7799 NP_001070868 P94S not found in SNVbox database
9540 NP_109597 K118R not found in SNVbox database
113 NP_705833 E599K not found in SNVbox database
621 NP_705833 K15R not found in SNVbox database
626 NP_705833 E774K not found in SNVbox database
859 NP_001070868 R423C not found in SNVbox database
1179 NP_001070868 L265P not found in SNVbox database
1282 NP_001070868 D77N not found in SNVbox database
1350 NP_705833 G406E not found in SNVbox database
1369 NP_001070868 K607R not found in SNVbox database
2252 NP_001070868 E656Q not found in SNVbox database
2505 NP_705833 F767Y not found in SNVbox database
2821 NP_705833 S656N not found in SNVbox database
3007 NP_001070868 S763P not found in SNVbox database
3085 NP_001070868 G14R not found in SNVbox database
3171 NP_705833 I535M not found in SNVbox database
3448 NP_705833 A127G not found in SNVbox database
3851 NP_705833 K795N not found in SNVbox database
3939 NP_001070868 K646N not found in SNVbox database
4105 NP_001070868 K95Q not found in SNVbox database
4247 NP_705833 K532E not found in SNVbox database
4311 NP_001070868 G663R not found in SNVbox database
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:52601701 A>G maps to NM_138932.2 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr16:7759117 C>T maps to NM_145891.2 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:9251208 C>T maps to NM_000014.4 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr12:9006739 T>C maps to NM_144670.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:44279823 C>T maps to NM_020745.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr17:79098601 C>T maps to NM_001080395.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr17:79098648 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:79093210 G>A maps to NM_001080395.2 H1351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:79100339 C>T maps to NM_001080395.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:107547871 C>T maps to NM_005502.3 P2150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:107578477 C>T maps to NM_005502.3 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr7:48318517 T>A maps to NM_152701.3 L2576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr7:48314896 C>T maps to NM_152701.3 S1878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr7:48314641 T>A maps to NM_152701.3 I1793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:48452146 G>A maps to NM_152701.3 T4142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:139904721 C>T maps to ENST00000355090 A2122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr16:2338027 G>A maps to NM_001089.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2373686 C>T maps to NM_001089.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:2327928 T>C maps to NM_001089.2 Q1620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr16:2374446 G>A maps to NM_001089.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:67109492 A>G maps to NM_080284.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1052085 G>A maps to NM_019112.3 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:1062284 C>T maps to NM_019112.3 R1895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:1054582 C>T maps to NM_019112.3 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr17:66918383 T>C maps to NM_007168.2 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:66928469 C>T maps to NM_007168.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:67031881 A>G maps to NM_080283.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:169853219 G>A maps to NM_003742.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:20725365 T>G maps to NM_001163941.1 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr16:16162159 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:16184365 G>T maps to ENST00000399408 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:16230426 C>T maps to ENST00000399408 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:43399894 C>T maps to NM_033450.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43411699 C>T maps to NM_033450.2 Q788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43412934 T>C maps to NM_033450.2 Y943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43413668 G>A maps to NM_033450.2 G1093G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr16:48209257 G>A maps to NM_032583.3 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:48234213 C>T maps to NM_032583.3 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:48250030 T>C maps to NM_032583.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:48226457 C>T maps to NM_032583.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:48174765 A>G maps to NM_033226.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:48151201 C>T maps to NM_033226.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:48139231 G>A maps to NM_033226.2 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:48745034 A>C maps to NM_003786.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:48745034 A>C maps to NM_003786.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:95696539 C>T maps to NM_005845.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:95696539 C>T maps to NM_005845.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:95715013 A>G maps to NM_005845.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:183696386 G>A maps to NM_005688.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr16:16248756 C>T maps to NM_001171.5 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr12:21998614 C>T maps to NM_005691.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr4:146033390 T>C maps to NM_002940.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr6:30553421 C>T maps to NM_001025091.1 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:30545878 A>G maps to NM_001025091.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:150920890 G>A maps to NM_005692.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:119025269 G>A maps to NM_001142505.1 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr11:119031693 C>T maps to NM_001142505.1 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:44078912 C>A maps to NM_022437.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr18:19283630 G>A maps to NM_138340.4 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:23072904 C>G maps to NM_022060.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr9:133729484 G>A maps to NM_007313.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:133759545 G>A maps to NM_007313.2 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:133761000 A>G maps to NM_007313.2 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:133755527 A>G maps to NM_007313.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:133760028 C>G maps to NM_007313.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:133760379 C>G maps to NM_007313.2 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:133755527 A>G maps to NM_007313.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:133760028 C>G maps to NM_007313.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:133761000 A>G maps to NM_007313.2 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr10:116331142 G>A maps to ENST00000277895 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:116203800 A>C maps to ENST00000277895 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr7:150557672 C>T maps to ENST00000416793 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr17:970325 G>A maps to NM_021962.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:970418 G>A maps to NM_021962.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:34226139 G>T maps to NM_145804.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:35470030 T>G maps to NM_198834.1 R2148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:109637233 G>T maps to NM_001093.3 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:134131032 C>T maps to NM_014384.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:211068099 A>G maps to NM_001608.3 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr10:124810590 G>A maps to NM_001609.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr11:44092849 C>T maps to NM_032592.3 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr23:15612968 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:19450597 G>C maps to NM_001010887.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:32433802 C>A maps to NM_002197.2 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr14:74008215 C>G maps to NM_001037161.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:55073629 C>T maps to NM_015547.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:6324746 G>A maps to NM_007274.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:58517519 A>G maps to NM_003500.3 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:58517519 A>G maps to NM_003500.3 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:11685947 A>G maps to NM_001111036.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:141006161 G>A maps to NM_001037172.1 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:25038483 G>A maps to NM_032501.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:25003704 A>C maps to NM_032501.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:229567383 G>T maps to NM_001100.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:5568299 A>T maps to NM_001101.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr17:79479256 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74140615 C>T maps to NM_001615.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:236908052 C>T maps to NM_001103.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:37394987 G>A maps to NM_024855.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52370180 G>A maps to NM_020328.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:38523753 C>T maps to NM_001106.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52308343 G>A maps to NM_001077401.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:127824166 C>T maps to NM_003474.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:39537615 C>T maps to NM_014237.2 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:70924431 C>T maps to NM_003813.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr7:87765307 C>T maps to NM_021723.3 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:24184087 G>T maps to NM_014265.4 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:24167699 G>A maps to NM_014265.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr4:175899129 G>A maps to NM_014269.4 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:39044564 G>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:39068683 T>A maps to NM_145004.5 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:24333984 C>T maps to ENST00000380789 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr8:38899581 C>A maps to NM_003816.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:24256388 A>T maps to NM_014479.3 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:24256511 T>C maps to NM_014479.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:24261517 G>A maps to NM_014479.3 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:28214237 T>C maps to NM_006988.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr9:136310908 G>A maps to NM_139025.3 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:72520416 A>G maps to NM_139155.2 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:130318934 C>A maps to NM_139055.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:77327041 C>T maps to NM_199355.2 Q1040Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:77325284 G>A maps to NM_199355.2 R1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:129001246 G>A maps to NM_133638.3 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr5:128863469 G>C maps to NM_133638.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:178564905 G>A maps to NM_014244.4 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:178552114 G>A maps to NM_014244.4 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:178549747 G>T maps to NM_014244.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr4:73205309 G>A maps to NM_014243.1 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:28315840 G>A maps to NM_007038.3 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:64756135 C>T maps to NM_197941.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:79065482 G>A maps to ENST00000258883 H691H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:79058985 C>T maps to ENST00000258883 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:130284494 C>T maps to NM_007037.4 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:64606839 C>A maps to NM_182920.1 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:64606791 C>T maps to NM_182920.1 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr9:18680513 G>A maps to NM_001040272.4 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr9:136404948 C>T maps to ENST00000393061 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1506798 C>T maps to NM_213604.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:154560613 G>A maps to ENST00000292205 T1045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr21:46595933 G>A maps to NM_015833.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:1405834 G>A maps to NM_018702.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:1246059 C>T maps to NM_018702.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr14:78392247 C>T maps to NM_020421.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140374481 G>C maps to NM_052853.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:41198209 A>G maps to NM_024876.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr19:41216027 G>T maps to NM_024876.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:45701761 C>T maps to NM_021116.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:7690871 G>A maps to NM_020546.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:7706988 C>T maps to NM_020546.2 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr14:24802152 G>A maps to NM_139247.3 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:50344626 C>T maps to NM_001114.3 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr16:4016486 C>T maps to NM_001116.3 A1117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:2896418 G>A maps to NM_014189.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:100237168 C>T maps to NM_000668.4 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:202915675 G>A maps to NM_015999.3 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:50921163 A>C maps to NM_024866.4 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr10:64565346 C>G maps to NM_032804.5 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:112838134 C>G maps to NM_000681.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:96780862 C>G maps to NM_000682.5 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:115804122 C>T maps to NM_000684.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:115804205 G>T maps to NM_000684.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:67052321 C>T maps to NM_001619.3 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:60883191 G>A maps to NM_175573.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:148695858 C>T maps to NM_152406.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:116056778 C>T maps to NM_001001936.1 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:148035199 G>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:148035199 G>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:148048493 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:147743485 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:74316460 C>T maps to NM_001134.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr4:178355533 A>G did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr12:58131510 G>A maps to NM_001122772.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:51769057 G>A maps to NM_001077665.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:86790935 C>T maps to NM_152336.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:228401668 T>C maps to NM_001135187.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:100353653 A>C maps to ENST00000311030 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:100340285 G>A maps to ENST00000311030 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139571559 G>A maps to NM_006412.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:139568308 G>A maps to NM_006412.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:45389033 C>T maps to NM_001037553.1 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:161567600 G>A maps to NM_020133.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:178364362 A>C maps to NM_003659.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:978799 C>T maps to NM_198576.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:985376 C>T maps to NM_198576.2 C1613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:67516604 G>C maps to NM_001138.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:88248238 T>C maps to ENST00000395847 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:88204461 A>G maps to ENST00000395847 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:115304548 G>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:115303836 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:115303933 T>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:247013202 G>A maps to ENST00000428671 N2073N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:247007231 T>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:247051713 A>G maps to ENST00000428671 Y788Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr14:105418967 G>C maps to NM_138420.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105415898 A>G maps to NM_138420.2 A1963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105416774 C>A maps to NM_138420.2 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105417731 G>A maps to NM_138420.2 D1352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105417737 G>C maps to NM_138420.2 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105417776 C>T maps to NM_138420.2 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:105416993 A>G maps to NM_138420.2 V1598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:105410416 G>A maps to NM_138420.2 L3791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:105413219 A>C maps to NM_138420.2 L2856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:105413648 A>G maps to NM_138420.2 D2713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr5:427977 G>A maps to NM_020731.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr1:26655286 C>T maps to NM_001039775.3 V1464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:67258361 C>A maps to NM_003977.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:6337403 G>A maps to NM_014336.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45712982 T>C maps to NM_000383.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:45712982 T>C maps to NM_000383.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr13:42877900 C>T maps to NM_016248.2 A1673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr13:42876625 C>A maps to NM_016248.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr13:42875257 T>C maps to NM_016248.2 Y792Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:49961618 C>T did not map to a codon.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr23:49957129 C>G did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:33014875 C>T maps to NM_004274.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:15484045 C>T maps to NM_005858.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15512392 G>A maps to NM_014371.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:91730337 C>T maps to NM_005751.4 L3689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:91660860 T>C maps to NM_005751.4 N1427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:109827527 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:88385578 G>A maps to NM_018064.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117099573 A>G maps to NM_030767.4 P1360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117104367 G>A maps to NM_030767.4 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:109395229 A>G maps to NM_152763.3 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:5042788 A>G maps to NM_001354.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105238782 G>A maps to NM_001014432.1 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:105239893 C>T maps to NM_001014432.1 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:105239893 C>T maps to NM_001014432.1 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:53526365 T>C maps to ENST00000425875 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:55041424 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:55039958 G>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:74285262 A>G maps to NM_000477.5 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:74280773 A>C maps to NM_000477.5 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49967995 G>A maps to NM_153329.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49969500 G>A maps to NM_153329.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49969521 C>T maps to NM_153329.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:101432797 C>G maps to NM_000693.2 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr9:38397088 G>A maps to NM_000692.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:125854403 C>T maps to ENST00000273450 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:125928394 A>G maps to NM_001182.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:125928394 A>G maps to NM_001182.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:135254033 G>A maps to NM_022568.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr1:165652257 C>T maps to NM_000696.3 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:101980706 A>G maps to NM_033087.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:183962999 A>G maps to NM_005787.5 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr11:77815051 A>G maps to NM_024079.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:29416749 A>G maps to NM_004304.3 Y1401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:29445424 G>A maps to NM_004304.3 S1136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:30143258 G>T maps to NM_004304.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:29543662 T>C maps to NM_004304.3 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:29940528 A>T maps to NM_004304.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:29543698 G>A maps to NM_004304.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:29416614 G>A maps to NM_004304.3 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:29449818 C>T maps to NM_004304.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:29449818 C>T maps to NM_004304.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:30143498 G>C maps to NM_004304.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:6374228 C>A maps to NM_032306.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:107427615 C>G maps to ENST00000417449 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr2:73677594 C>A maps to NM_015120.4 S1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:73676188 C>T maps to NM_015120.4 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:73676314 A>G maps to NM_015120.4 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:73829361 G>A maps to NM_015120.4 R4054R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:73646369 G>A maps to NM_015120.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4539170 G>T maps to NM_001140.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:7950008 C>G maps to NM_001141.2 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:233322999 C>T maps to NM_001631.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:233322285 C>T maps to NM_001631.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr18:56246642 G>T maps to NM_052947.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr18:56171334 C>T maps to NM_052947.3 P2025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:85400563 C>T maps to NM_020778.4 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:233243792 C>T maps to NM_001632.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:233243795 T>C maps to NM_001632.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:233271851 C>T maps to NM_031313.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:44286721 C>T maps to NM_021926.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:33520903 G>A maps to NM_152462.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7385773 C>T maps to NM_001102614.1 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:71469005 C>T maps to NM_016519.4 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:46456443 G>A maps to ENST00000458649 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2578130 C>G maps to NM_001145815.1 L233L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6907-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:118085544 A>G maps to NM_001098526.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr23:112065818 A>G did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:112033850 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:112022686 T>C did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:112053137 C>T did not map to a codon.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr23:112035108 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:94602456 G>A maps to NM_130847.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr11:94554797 G>A maps to NM_130847.2 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:10526178 C>T maps to NM_000480.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:2752025 G>A maps to NM_133463.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr7:2748853 C>T maps to NM_133463.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73992861 C>G maps to NM_173473.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:73992861 C>G maps to NM_173473.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr20:865838 G>A maps to NM_015985.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:854972 T>G maps to NM_015985.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:861852 G>A maps to NM_015985.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:178834230 T>C maps to NM_004673.3 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:41552839 G>A maps to ENST00000415018 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:114279769 T>C maps to NM_001148.4 S3332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:61830255 T>C maps to NM_020987.2 Q3461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:61832130 A>G maps to NM_020987.2 H2836H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr17:54403698 C>T maps to NM_153228.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:139917068 C>T maps to ENST00000253810 R2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr5:139818109 G>A maps to ENST00000253810 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr16:89348401 G>A maps to NM_013275.4 D1516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:27939426 G>C maps to NM_152345.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr4:74005712 G>A maps to NM_032217.3 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:33131226 C>T maps to NM_032139.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr18:21197728 C>T maps to NM_173505.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr18:14797833 C>T maps to NM_001145029.1 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52282864 C>T maps to NM_182608.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:98201526 G>A maps to NM_025190.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:48774318 G>A maps to NM_052855.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:132150803 G>A maps to NM_175873.4 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173596272 A>G maps to ENST00000367712 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:56638454 G>A maps to NM_173595.3 N901N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:71212379 C>A maps to NM_001115116.1 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr4:77818939 C>T maps to NM_001029870.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:118893022 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:118893389 A>G did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr6:34957032 G>A maps to NM_015245.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:99139558 G>T maps to NM_181670.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr9:101518729 G>T maps to ENST00000375018 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr11:70009434 C>T maps to NM_018043.5 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:5841700 C>T maps to ENST00000356134 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr11:26538444 A>C maps to NM_031418.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr11:26664762 G>A maps to NM_031418.2 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:101520846 G>A maps to ENST00000392977 *956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:242147053 G>A maps to NM_001001891.3 W403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:242144307 G>A maps to NM_001001891.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr4:165118818 C>T maps to NM_012403.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr4:80899205 T>C maps to NM_001145794.1 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr10:81932569 A>T maps to NM_145869.1 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:16318903 G>C maps to NM_001130524.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:77423964 A>C maps to NM_003664.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr5:77412010 A>T maps to NM_003664.3 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:83378365 G>A maps to NM_004644.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2116615 T>C maps to ENST00000355272 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:99704103 G>A maps to ENST00000429084 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:29398913 C>T maps to NM_005503.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:29368268 G>A maps to NM_005503.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:3760055 G>A maps to NM_004886.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:112176555 G>A maps to NM_001127510.2 A1755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:112162853 T>C maps to NM_001127510.2 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:112164560 G>A maps to NM_001127510.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:112176324 G>A maps to NM_001127510.2 G1678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:112176558 T>G maps to NM_001127510.2 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:112177170 G>A maps to NM_001127510.2 P1960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1469029 A>G maps to NM_005883.2 K1910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1469077 G>A maps to NM_005883.2 S1926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr3:49718541 G>A maps to ENST00000438011 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:36370091 C>T maps to NM_001024807.1 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr2:21239441 C>T maps to NM_000384.2 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:39357633 A>G maps to NM_001193289.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:39380130 C>T maps to ENST00000402182 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:39381956 C>T maps to ENST00000402182 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:39381935 G>A maps to ENST00000402182 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:56755299 A>C maps to NM_001638.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:36623578 T>A maps to ENST00000451256 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr22:36122573 C>T maps to NM_030642.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:36054943 C>T maps to NM_030641.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:27326976 A>G maps to NM_000484.3 Y538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:58603184 G>C maps to NM_006380.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:77301384 G>A maps to NM_173039.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:241631498 G>A maps to ENST00000429564 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:50344957 C>T maps to NM_000486.5 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:25228565 G>A maps to NM_001169.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr5:115351065 T>A maps to NM_173800.4 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr5:115299000 C>T maps to NM_173800.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:115351065 T>A maps to NM_173800.4 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:66905871 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:66937417 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:72403831 T>C did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr4:36069897 A>G maps to NM_015230.2 S1582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:143694519 C>T maps to NM_015193.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr11:118463476 G>A maps to ENST00000359415 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr20:61907882 G>A maps to NM_175609.1 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:47588948 G>A maps to NM_006420.2 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:32925225 T>G maps to NM_014783.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:24965974 C>G maps to NM_001006634.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr10:24880820 G>A maps to NM_020824.3 Q1333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr1:161026255 G>A maps to NM_001025598.1 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:128994780 G>A maps to NM_001142685.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:128842602 G>A maps to NM_001142685.1 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:11160429 A>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:11682920 C>A did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:45221389 C>T maps to ENST00000352766 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:45258342 C>T maps to ENST00000352766 H600H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:57867906 G>A maps to ENST00000393797 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:57869680 G>A maps to ENST00000393797 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:42409188 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:1808342 C>T maps to ENST00000398564 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:1905221 A>G maps to ENST00000398564 S1301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:156931507 C>T maps to NM_198236.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:155931629 G>A maps to NM_001162383.1 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:155935157 T>C maps to NM_001162383.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr1:155928158 T>G maps to NM_001162383.1 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr2:131799002 C>T maps to NM_015320.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:131803623 C>T maps to NM_015320.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr1:27056216 C>T maps to NM_006015.4 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr1:27102082 G>A maps to NM_006015.4 W1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:157505477 G>A maps to ENST00000367148 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr12:46244015 C>T maps to NM_152641.2 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:46245076 G>A maps to NM_152641.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:58831257 A>C maps to NM_002892.3 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:235357459 A>G maps to NM_016374.5 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr10:63662067 C>T maps to NM_032199.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:41477669 G>A maps to NM_001661.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr1:202113678 G>A maps to NM_138795.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:66517548 T>C maps to NM_018120.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31477441 T>C maps to ENST00000408912 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:31471282 G>A maps to ENST00000408912 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr3:138009386 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:100912064 C>T did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:101858510 C>T did not map to a codon.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr23:101858322 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:27543027 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:18121453 G>C maps to NM_015683.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr15:98512602 C>G maps to NM_183376.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr23:2873469 G>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:2852956 C>G did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:3021804 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:2990196 T>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:3021869 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:66397520 C>T maps to NM_014960.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:66416510 C>T maps to NM_014960.3 N495N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:149677634 G>A maps to NM_001012301.2 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:94936743 G>A maps to NM_198150.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr11:3661043 G>A maps to NM_001079536.1 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:19969494 G>T maps to NM_001670.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:19969586 G>A maps to NM_001670.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:52005056 T>C maps to NM_019893.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr1:23779192 T>C maps to NM_017707.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:15301724 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr23:63444982 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42248204 C>T maps to NM_080863.4 L16L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:76387794 C>T maps to NM_080868.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:94405615 G>A maps to ENST00000434324 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:132401752 G>A maps to NM_017873.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:7004926 C>T maps to NM_080912.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:32856837 C>A maps to NM_001672.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:32856837 C>A maps to NM_001672.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:65551781 G>A maps to NM_000048.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:1522324 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:1522329 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:1531700 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:79943474 A>G maps to ENST00000306729 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:79941510 C>T maps to ENST00000306729 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:79941510 C>T maps to ENST00000306729 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:119770494 G>A maps to ENST00000313400 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31022479 C>T maps to ENST00000375687 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr2:25966253 T>C maps to NM_018263.4 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr2:25966277 T>C maps to NM_018263.4 E976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr18:31326553 C>T maps to NM_030632.1 R2248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:124357252 G>A maps to NM_014109.3 H863H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:124360486 G>A maps to NM_014109.3 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:1458943 C>T maps to NM_018188.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:1458149 T>C maps to NM_018188.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:123670574 G>T maps to NM_001001976.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:39917560 C>T maps to NM_182810.1 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32093921 G>A maps to NM_004381.4 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:53925572 C>T maps to NM_001130059.1 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:14577523 C>T maps to NM_018179.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr14:96771960 T>A maps to NM_018036.5 G1566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:96829301 C>T maps to NM_018036.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:107396260 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:220088467 A>G maps to NM_024085.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:290887 G>A maps to ENST00000409479 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:290049 G>A maps to ENST00000409479 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:108163486 C>T maps to NM_000051.3 P1526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:108163486 C>T maps to NM_000051.3 P1526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr12:7045905 G>A maps to NM_001940.3 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr4:94750976 C>T maps to NM_005172.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:94750226 G>A maps to NM_005172.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:94750649 C>T maps to NM_005172.1 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr4:94751126 G>A maps to NM_005172.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:69991098 G>A maps to NM_145178.2 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:25928507 C>T maps to NM_024490.3 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:25962056 C>T maps to NM_024490.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:160115006 C>T maps to NM_025153.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr13:25255704 C>A maps to NM_001185085.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr13:25272806 C>T maps to NM_001185085.1 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:25255704 C>A maps to NM_001185085.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr13:25285536 C>T maps to NM_001185085.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:19766364 G>A maps to NM_020410.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:194157936 G>A maps to NM_024524.3 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:193120458 G>A maps to NM_032279.2 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:193120626 C>T maps to NM_032279.2 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:193272555 C>T maps to NM_032279.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:160090992 G>A maps to NM_000702.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:160104949 C>T maps to NM_000702.3 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:160129272 G>A maps to NM_144699.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:28898777 C>G maps to NM_173201.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:28898777 C>G maps to NM_173201.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:110765377 G>A maps to NM_170665.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3850909 A>G maps to NM_174953.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:152830494 T>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:203669370 G>A maps to NM_001001396.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:130698204 C>T maps to NM_001001486.1 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:40464821 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:138417681 G>A maps to NM_130840.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:104054602 T>C maps to NM_001695.4 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:50212571 G>T maps to NM_024837.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr20:50313971 G>A maps to NM_006045.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:50310558 G>A maps to NM_006045.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:117075139 A>C maps to NM_207303.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:76907650 G>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:111907955 G>C maps to NM_002973.3 S1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr7:105254602 G>A maps to NM_020725.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:74756499 G>A maps to ENST00000258081 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr2:74756625 C>T maps to ENST00000258081 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr1:1309460 G>A maps to NM_001127230.1 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:1309802 G>A maps to NM_001127230.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:57743517 C>T maps to NM_001015878.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:70239033 C>T maps to NM_015570.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:58197373 C>A maps to NM_006576.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:69455670 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr23:69261725 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:831810 C>T maps to NM_001700.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:831864 G>A maps to NM_001700.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:235647808 C>T maps to ENST00000366599 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr6:71571676 A>G maps to NM_080742.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:62449663 G>A maps to NM_006577.5 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr19:41932419 G>A maps to NM_198540.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:67183866 C>T maps to NM_033309.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:644350 A>G maps to NM_173593.3 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:380389 C>T maps to NM_178537.4 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:19246666 A>G maps to NM_015681.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:117186505 G>A maps to NM_012104.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:90718536 G>A maps to NM_001170794.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:38034401 G>A maps to NM_004874.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:11049615 C>T maps to NM_182482.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr8:143625723 C>T maps to NM_001702.2 G1567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:143599593 C>T maps to NM_001702.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:69348965 A>C maps to NM_001704.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1391361 A>G maps to NM_003933.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1391418 T>C maps to NM_003933.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr16:88039848 G>A maps to NM_001173543.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:88071610 C>T maps to NM_001173543.1 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr16:88039845 C>T maps to NM_001173543.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:31503218 G>A maps to ENST00000417556 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:31599555 A>C maps to NM_080686.2 R1036R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:31603045 C>T maps to NM_080686.2 D1766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:31602133 T>G maps to NM_080686.2 L1614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr9:134322482 G>A maps to NM_013318.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:171553208 C>T maps to ENST00000392078 S2508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:171509274 T>C maps to ENST00000392078 D890D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr14:35231203 A>G maps to NM_013448.2 R1334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:160241784 T>C maps to NM_013450.2 G1189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:27148846 G>A maps to NM_003986.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr4:123664880 G>T maps to NM_152618.2 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170336101 C>G maps to ENST00000419050 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:156621251 G>A maps to NM_021948.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:94049575 A>G maps to NM_003567.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:58952043 G>A maps to ENST00000407086 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr20:49411688 G>T maps to NM_198799.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:25031514 T>C maps to NM_001178093.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:24970965 G>A maps to NM_001178093.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:127541742 A>G maps to NM_016567.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:85733327 A>G maps to NM_003921.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr14:99641015 C>G maps to NM_138576.2 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr14:99641822 C>T maps to NM_138576.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr18:60985443 C>T maps to NM_000633.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:60985832 G>A maps to NM_000633.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr18:60985869 A>G maps to NM_000633.2 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr15:80263050 G>A maps to NM_004049.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:147091688 G>A maps to NM_004326.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:118770053 G>A maps to NM_182557.2 N1190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:118773203 G>A maps to NM_182557.2 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:39933242 A>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:39932948 G>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:39932807 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:23523317 C>T maps to NM_004327.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:23523321 C>T maps to NM_004327.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:23523330 T>C maps to NM_004327.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:219527856 G>A maps to NM_004328.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr14:101004956 G>A maps to NM_020836.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:13481465 C>T maps to ENST00000396900 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:61730413 C>A maps to NM_001139443.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr12:70087574 G>A maps to NM_032735.2 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:205397 G>A maps to NM_001098787.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102004045 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102005370 A>T did not map to a codon.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr23:102004883 G>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:32458755 C>T maps to NM_001714.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:32480885 T>C maps to NM_001714.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:32481368 C>T maps to NM_001714.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:127827597 C>T maps to NM_139343.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:127809839 C>A maps to NM_139343.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:127811560 G>A maps to NM_139343.1 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:102195296 G>A maps to NM_182962.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:102195983 T>A maps to NM_182962.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr2:32724812 C>T maps to NM_016252.3 R2890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:32673883 A>G maps to NM_016252.3 P1502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr2:32773074 T>C maps to NM_016252.3 L4323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr19:53793121 G>T maps to NM_033341.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:103460018 G>A maps to NM_017693.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:102046401 G>C maps to NM_173809.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr19:40964384 G>A maps to NM_000713.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr8:22052355 G>A maps to NM_006129.4 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:22059412 C>G maps to NM_006129.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:50659591 T>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:79832487 A>G maps to NM_198892.1 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr6:55659188 G>T maps to NM_021073.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:39988707 A>G maps to NM_181809.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:33946463 C>T maps to NM_133468.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:34091569 T>G maps to NM_133468.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:15555338 G>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:172578594 T>C maps to NM_013979.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:172581386 A>G maps to NM_013979.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:112993411 C>T maps to ENST00000273395 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:112989762 C>T maps to ENST00000273395 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31598908 G>A maps to NM_025227.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:32843311 G>A maps to NM_174932.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:65914910 T>C maps to ENST00000321892 D1921D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:65919091 G>A maps to ENST00000321892 R2024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140449149 T>C maps to NM_004333.4 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140481424 T>C maps to NM_004333.4 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:140449149 T>C maps to NM_004333.4 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:140449149 T>C maps to NM_004333.4 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr12:112082104 C>T maps to NM_006768.3 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:41245642 A>G maps to ENST00000471181 N635N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr13:32906688 G>A maps to NM_000059.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50217386 G>A maps to ENST00000342989 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:50217299 G>A maps to ENST00000342989 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:50217386 G>A maps to ENST00000342989 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr22:50217386 G>A maps to ENST00000342989 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:32948430 C>G maps to ENST00000395289 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:15349961 G>A maps to NM_058243.2 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:105707746 C>T maps to NM_001519.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:36177596 C>T maps to NM_015695.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:135574269 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55815071 C>T maps to NM_032430.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55823420 G>C maps to NM_032430.1 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:55817693 C>T maps to NM_032430.1 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:40590175 G>T maps to NM_018963.3 G1187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:40608529 A>C maps to NM_018963.3 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:40582822 C>T maps to NM_018963.3 T1311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:80064531 G>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:49692748 C>T maps to NM_003458.3 A1920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:49698694 T>C maps to NM_003458.3 R3139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:83725290 T>A maps to NM_025238.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:108011970 G>A maps to NM_001018072.1 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:15686610 C>T maps to NM_000060.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr12:92539199 G>A maps to NM_001731.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr12:92539202 G>A maps to NM_001731.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr12:92539202 G>A maps to NM_001731.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:92539245 G>A maps to NM_001731.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:92538170 G>C maps to NM_001731.2 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:92539188 G>A maps to NM_001731.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr12:92539170 C>T maps to NM_001731.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr12:92539202 G>A maps to NM_001731.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:203276374 C>T maps to NM_006763.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:203274877 T>C did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:203276286 C>G maps to NM_006763.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:203274835 G>A maps to NM_006763.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:203274875 G>T maps to NM_006763.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr1:203274835 G>A maps to NM_006763.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:203276386 C>T maps to NM_006763.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:100617217 A>G did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:100612564 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr23:100613633 A>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:26374570 G>A maps to NM_001197246.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr15:40453451 C>T maps to ENST00000412359 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:40453429 G>T maps to ENST00000412359 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:40512905 A>G maps to ENST00000412359 K1047K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:56388355 C>T maps to NM_004758.2 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:121602829 G>A maps to NM_024834.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:124457479 A>G maps to NM_001010912.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr10:127429568 G>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:5803348 A>C maps to NM_017782.4 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:120489827 G>A maps to NM_153810.4 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:11912380 G>A maps to NM_153256.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:50531519 C>A maps to NM_001135196.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:50531906 C>T maps to NM_001135196.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr10:128193432 C>T maps to NM_001004298.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:556583 G>A maps to NM_173573.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr11:33667419 C>T maps to ENST00000389726 H1575H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr11:33667497 G>A maps to ENST00000389726 P1601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:61254454 T>C maps to NM_145017.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr11:109294502 G>A maps to NM_207645.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr12:27070327 T>G maps to NM_018164.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:82780675 A>G maps to NM_032230.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:110206759 C>A maps to NM_032829.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr12:112622062 G>A maps to NM_001109662.2 S3397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:112600882 C>T maps to NM_001109662.2 P4189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr12:113624823 C>T maps to NM_032848.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr12:10339159 C>T maps to NM_153022.2 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:90745441 T>C maps to NM_017970.2 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:45693647 G>A maps to NM_018353.4 C714C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr14:45693170 A>G maps to NM_018353.4 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:93652733 C>T maps to NM_001098621.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:91666247 T>C maps to NM_001102368.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:91666130 C>T maps to NM_001102368.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:91666247 T>C maps to NM_001102368.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:77843919 A>G maps to NM_001010860.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:24771171 G>A maps to NM_174913.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:24772964 C>A maps to NM_174913.1 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr14:24771449 A>G maps to NM_174913.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:58604729 T>C maps to ENST00000438670 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:58605155 G>A maps to ENST00000438670 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr14:77493808 C>T maps to NM_024496.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr14:77493790 C>T maps to NM_024496.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:77493808 C>T maps to NM_024496.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr14:77493826 T>C maps to NM_024496.2 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:24923128 T>C maps to NM_018958.2 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr15:75500342 C>T maps to NM_015492.4 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:83673652 A>C maps to NM_001160114.1 V146V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6907-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:36989577 C>T maps to NM_001130010.1 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:90145117 T>A maps to NM_152259.3 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:90164768 T>C maps to NM_152259.3 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr16:31510676 A>G maps to NM_022744.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31505251 C>T maps to NM_022744.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:31502227 G>A maps to NM_022744.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:19590443 T>C maps to NM_020314.5 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89778918 T>C maps to NM_004913.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:89774869 C>T maps to NM_004913.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:89783204 G>A maps to NM_004913.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:19726123 G>A maps to NM_001012991.2 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:5115810 G>A maps to ENST00000350219 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr16:30770511 T>C maps to NM_001014979.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:80364340 C>T maps to NM_175902.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:45471442 G>A maps to NM_152347.4 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:58506784 G>T maps to NM_181707.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:8135445 G>A maps to NM_025099.5 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:8141778 T>C maps to NM_025099.5 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:8135445 G>A maps to NM_025099.5 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:16347000 C>T maps to NM_001113567.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:72588437 G>T maps to NM_152460.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3728314 C>T maps to NM_001114118.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:79632326 C>T maps to NM_001039842.1 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:47008735 G>A maps to NM_001035005.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr18:30950117 G>A maps to NM_001105528.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr18:30928851 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:507559 G>A maps to NM_033513.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:507730 C>T maps to NM_033513.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:757353 G>A maps to NM_173481.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:757482 G>A maps to NM_173481.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:757233 C>T maps to NM_173481.2 R96R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FF-8047-01A-11D-2210-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G8-6909-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:41248531 G>A maps to NM_198476.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:22987743 C>T maps to NM_000491.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:119915749 G>T maps to NM_182528.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr17:77043848 C>T maps to ENST00000392445 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr5:159781843 G>A maps to NM_031908.4 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:244715881 A>G maps to NM_001130957.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:200860730 G>A maps to NM_018265.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:38155318 C>T maps to NM_017850.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:162824959 G>A maps to NM_178550.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:169796858 A>C maps to NM_018186.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:231487132 G>A maps to NM_032018.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:11009678 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:11009678 G>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:11017140 G>A maps to NM_001170754.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:12819400 G>A maps to NM_152290.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:57185999 G>A maps to NM_001004303.4 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:55277552 C>T maps to NM_001110533.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:228290222 G>C maps to NM_024319.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr1:150256252 C>T maps to NM_144697.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:197872000 G>A maps to NM_001024594.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr1:233113955 C>T maps to NM_032324.1 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:156377719 G>A maps to ENST00000357975 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:16332642 C>G maps to NM_178840.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:43870070 C>A maps to ENST00000310739 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr1:60491071 C>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:226785101 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:55108507 G>A maps to NM_001013646.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:54940147 C>T maps to NM_080821.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:31044058 G>A maps to NM_080616.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:60989242 T>C maps to NM_080833.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31644435 A>C maps to NM_182658.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31661398 C>T maps to NM_182658.1 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:31671410 C>T maps to NM_182519.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr20:3302909 C>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:20055847 A>G maps to ENST00000389655 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:24954302 G>C maps to NM_020531.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:24954302 G>C maps to NM_020531.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr20:24959518 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:5086917 G>A maps to NM_001009923.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:5086917 G>A maps to NM_001009923.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:744509 G>A maps to NM_033409.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:13797178 G>A maps to NM_024120.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31761884 G>T maps to NM_080574.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31812948 C>T maps to NM_178466.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:56735760 C>T maps to NM_178456.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr20:10603705 G>A maps to NM_001009608.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr21:45753030 C>T maps to ENST00000397956 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45755645 C>T maps to ENST00000397956 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45929191 G>A maps to ENST00000443468 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45953575 C>T maps to ENST00000443468 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr21:45948341 C>T maps to ENST00000443468 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:45949768 G>A maps to ENST00000443468 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr21:47581868 G>A maps to NM_001142854.1 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:47588426 G>A maps to NM_001142854.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:47734776 G>A maps to NM_058180.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:37397875 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:24984260 G>A maps to NM_207644.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:45608214 G>A maps to NM_015264.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:27802456 T>C maps to NM_032266.3 G1006G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:27803809 C>T maps to NM_032266.3 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:27799711 G>A maps to NM_032266.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:220041490 C>T maps to NM_015680.4 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:70387825 C>A maps to NM_017880.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:24260861 A>G maps to NM_025203.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:29293836 C>T maps to NM_001029883.1 Q1097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170537660 A>G maps to NM_001085447.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:242814603 G>C maps to NM_173821.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:242814777 C>T maps to NM_173821.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr2:63661024 G>A maps to NM_015910.4 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr19:6696417 G>A maps to NM_000064.2 T974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:119445138 A>G maps to NM_033364.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:14769979 G>A maps to NM_032137.4 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:126270922 G>C maps to NM_152533.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:155493496 T>C maps to ENST00000340171 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr3:37458936 C>T maps to NM_178339.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:43122701 G>A maps to NM_032806.4 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr3:192516411 G>A maps to NM_178496.3 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:56667212 T>C maps to ENST00000447900 Q1202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr3:153203808 C>T maps to NM_001101337.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:207305068 A>C maps to NM_000715.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:207287445 C>G maps to NM_000715.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:113553097 G>A maps to NM_018392.4 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:71024466 T>G maps to NM_214711.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:71024472 T>A maps to NM_214711.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:56205558 C>T maps to NM_153706.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:2752509 G>A maps to NM_178569.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:37173976 A>G maps to NM_023073.3 A2017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:37182939 T>A maps to NM_023073.3 T1781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:37226887 A>G maps to NM_023073.3 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:37244668 C>T maps to NM_023073.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr5:147286046 A>G maps to NM_206966.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:125968300 C>T maps to NM_207408.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:41160292 A>G maps to NM_001115131.1 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:41181577 T>A maps to NM_001115131.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:43193876 G>A maps to ENST00000509253 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:43193876 G>A maps to ENST00000509253 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:30615412 T>C maps to NM_001161376.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:31079349 T>C maps to NM_014070.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43475194 G>A maps to NM_001012974.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:88046817 A>G maps to NM_020425.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:127797388 C>T maps to NM_001012279.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:4122278 A>G maps to NM_001085401.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:118953754 T>C maps to NM_001042475.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:151789706 T>A maps to NM_024573.1 L263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:151789727 T>A maps to NM_024573.1 L270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:35705058 G>A maps to NM_145028.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr6:151914337 C>T maps to ENST00000367290 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr5:40958154 G>A maps to NM_000587.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:40934470 G>A maps to NM_000587.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr5:40936441 C>T maps to NM_000587.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:2578923 G>A maps to NM_152743.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:150027801 C>T maps to NM_138434.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:148288134 C>T maps to NM_145304.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:92158153 G>A maps to NM_032120.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:33361279 C>T maps to NM_001102401.1 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr8:67796148 A>G maps to NM_173518.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:67813481 G>A maps to NM_173518.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:144652779 T>A maps to NM_001100878.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:10532187 T>C maps to NM_001040032.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:12879015 T>A maps to NM_020844.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:27925219 A>G maps to ENST00000341513 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr9:86258427 T>C maps to NM_001001551.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:131585085 G>C maps to NM_016390.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:139959230 G>A maps to NM_178448.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr9:12775860 T>C maps to NM_203403.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:12775854 T>C maps to NM_203403.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:135418388 G>A maps to NM_207417.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139740899 C>T maps to NM_001080482.2 N678N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140146525 G>A maps to ENST00000388931 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:34379661 T>A maps to NM_032596.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:34401048 C>T maps to NM_001184940.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:77632225 T>C maps to NM_152420.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr9:77614779 A>G maps to NM_152420.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:4625545 C>T maps to ENST00000454239 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr9:90499848 C>T maps to NM_178828.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:26842505 G>A maps to NM_024828.3 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:114454734 T>C maps to NM_173521.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:135601125 G>A maps to NM_152572.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr17:58227427 C>T maps to NM_000717.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:9009451 C>T maps to ENST00000413627 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr22:24447359 C>T maps to NM_012295.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:21736485 C>T maps to NM_012189.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:65142685 G>A maps to ENST00000371073 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:13323260 C>T maps to NM_023035.2 T2046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:13563766 G>A maps to NM_023035.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr12:2676735 C>T maps to NM_199460.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:181724380 C>T maps to ENST00000357570 F1279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:49061778 C>T did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:49083585 C>T did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:49088336 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:49070328 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:49081229 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1245061 C>T maps to NM_021098.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1255205 C>T maps to NM_021098.2 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:1268595 C>T maps to NM_021098.2 H1944H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:201058427 G>A maps to NM_000069.2 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:201058529 G>A maps to NM_000069.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:81593540 T>C maps to NM_000722.2 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr17:64881272 C>T maps to NM_145811.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:27447309 G>A maps to NM_004341.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:93108762 G>C maps to NM_001164737.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:105207175 G>A maps to NM_015916.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:47112206 C>T maps to NM_005184.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:9804657 G>A maps to NM_003656.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:114438739 C>T maps to ENST00000515496 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:75574955 G>A maps to ENST00000423381 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:183978935 G>A maps to NM_033259.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:110820115 T>G maps to NM_001744.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3786455 C>T maps to ENST00000381771 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr3:48265111 A>G maps to NM_004345.3 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:67699535 G>A maps to NM_018448.3 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:17426845 T>C maps to NM_006366.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:17507503 C>G maps to NM_006366.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39226162 G>A maps to NM_144691.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39227888 C>T maps to NM_144691.3 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39234673 G>A maps to NM_144691.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:39229074 C>T maps to NM_144691.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:42680057 T>C maps to NM_000070.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:42679976 C>T maps to NM_000070.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:42702835 C>T maps to NM_000070.2 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:76796021 C>A maps to ENST00000360841 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:76796081 G>A maps to ENST00000360841 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:110491864 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:113202385 C>T maps to NM_006135.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr22:37912257 G>A maps to NM_014550.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78176192 G>A maps to NM_024110.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139264826 C>T maps to NM_052813.4 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:8953029 C>T maps to NM_014316.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr13:111340365 C>A did not map to a codon.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr12:25297342 C>A maps to NM_018272.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:40916271 G>A maps to NM_170589.3 A1296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:94173773 C>T maps to NM_022900.4 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:41604808 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:2239542 C>T maps to NM_020764.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr11:104899974 C>T maps to NM_033292.2 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:142988725 G>A maps to NM_032982.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:104871192 A>G maps to NM_001136112.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr2:202141596 T>A maps to NM_001080125.1 C295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:202137431 A>G maps to NM_001080125.1 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:90577649 T>G maps to NM_012115.3 R1547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:160162590 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:134347240 T>C maps to NM_178019.2 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:92102818 G>A maps to NM_024764.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr10:74183071 G>A maps to NM_006077.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:74183033 G>A maps to NM_006077.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:32210967 G>A maps to NM_005093.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:67116168 C>T maps to NM_022845.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:119170361 C>T maps to NM_005188.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:119168129 G>C maps to NM_005188.2 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr3:105495384 G>A maps to NM_170662.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45285733 G>A maps to NM_012116.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:24898134 C>T maps to NM_001039771.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:54639962 G>A maps to NM_012117.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr10:70549638 G>A maps to NM_018237.2 T1120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr18:66721310 G>A maps to NM_024781.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35661087 G>A maps to NM_174923.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:35660871 C>T maps to NM_174923.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:219900299 A>C maps to NM_194302.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr18:47788543 T>G maps to NM_145020.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr18:47788543 T>G maps to NM_145020.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:185578336 C>T maps to NM_152683.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:21991223 C>T maps to NM_152612.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:33457327 C>T maps to NM_032816.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:33414391 T>C maps to NM_032816.3 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:31614237 C>T maps to NM_194300.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:92900575 T>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:42209766 C>T maps to NM_024821.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:123633664 T>C maps to NM_022757.4 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74708452 A>T maps to ENST00000393965 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:76891534 C>T maps to NM_020879.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:11537005 G>A maps to NM_145045.4 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49920718 C>T maps to NM_144688.4 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:30761994 G>A maps to NM_001017437.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:30765501 G>C maps to NM_001017437.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:77255209 C>T maps to NM_001042784.1 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:77272154 C>A maps to NM_001042784.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:77255209 C>T maps to NM_001042784.1 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:11465310 C>T maps to ENST00000427879 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:133378850 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:26581980 G>A maps to NM_022778.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:32669644 C>T maps to ENST00000421922 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr15:74623323 G>A maps to ENST00000321288 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:126142197 G>A maps to ENST00000505024 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:126137455 T>C maps to ENST00000505024 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:126142188 C>A maps to ENST00000505024 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78014023 G>A maps to NM_017950.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78032676 C>T maps to NM_017950.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr17:78032380 C>T maps to NM_017950.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:94702621 T>C maps to NM_001042399.1 K691K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr17:64125941 C>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:113175983 G>A maps to NM_144718.3 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:80146153 G>C maps to ENST00000445854 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:80059689 G>A maps to ENST00000445854 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr12:119942900 C>T maps to NM_178499.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:46520068 C>T maps to NM_001080402.1 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:49308260 C>T maps to NM_033124.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:56628032 C>T maps to NM_001141947.1 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:112356976 T>C maps to ENST00000447230 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr11:86131000 C>T maps to NM_001156474.1 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:86133615 G>T maps to NM_001156474.1 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:66359190 A>T maps to NM_018219.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:55615949 T>C maps to ENST00000436346 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:64120702 G>A maps to NM_032251.5 T1226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr14:91770134 G>T maps to NM_001080414.2 S1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:91770307 C>T maps to NM_001080414.2 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:91805803 C>T maps to NM_001080414.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:47774679 C>G maps to NM_015603.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124421763 C>T maps to NM_025140.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:31118303 C>T maps to NM_001105564.1 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:6291465 A>G maps to NM_176875.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:68471231 C>T maps to NM_031966.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:50085216 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:69462801 G>A maps to NM_053056.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:69457986 C>T maps to NM_053056.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr12:4383226 G>A maps to NM_001759.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:86695227 A>T maps to NM_001239.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:86708575 G>A maps to NM_001239.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:46401242 A>G maps to NM_001123041.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:167550740 C>A maps to NM_004367.5 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:62103326 G>T maps to NM_006430.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:10262606 G>A maps to NM_012073.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:17071898 G>A maps to NM_014406.4 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:17072346 C>T maps to NM_014406.4 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:74521947 G>T maps to NM_133493.3 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:74524723 G>A maps to NM_133493.3 V1263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:74524756 T>G maps to NM_133493.3 S1274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr5:140011944 G>A maps to NM_001174105.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:7636026 A>G maps to NM_004244.4 C1008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:158226645 C>G maps to NM_001763.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158299298 C>T maps to NM_001764.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:158151891 T>C maps to NM_001766.3 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:158151891 T>C maps to NM_001766.3 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158325764 C>T maps to NM_030893.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158325818 G>A maps to NM_030893.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:112648106 G>A maps to NM_138806.3 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:35831985 C>T maps to NM_001771.3 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:35835738 G>A maps to NM_001771.3 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:66083262 C>T maps to NM_020404.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr9:5457195 G>A maps to NM_014143.3 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:41926022 G>A maps to NM_145273.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr7:80285935 C>A maps to NM_001127444.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:80300448 T>G maps to NM_001127444.1 Y325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:35223302 G>A maps to NM_000610.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr17:80274178 A>G maps to NM_006137.6 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr19:42384802 G>T maps to NM_001783.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr17:62006832 A>G maps to NM_001039933.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:14118296 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr2:87085357 G>A maps to NM_172213.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr19:14512522 C>T maps to NM_078481.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:43028206 G>C maps to NM_138477.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:100856379 A>C maps to NM_033312.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:100928420 C>T maps to NM_033312.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:100933575 T>C maps to NM_033312.2 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr13:115002274 A>G maps to NM_003903.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:54424380 G>A maps to NM_001170402.1 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:137533900 C>T maps to NM_004661.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:137654979 G>A maps to NM_001790.3 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:227504744 A>G maps to ENST00000366766 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:103406168 C>T maps to NM_006035.3 R1569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:103434984 G>A maps to NM_006035.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:64594200 C>T maps to NM_017525.2 E1485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:65088497 T>C maps to NM_006779.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:44387304 T>C maps to NM_001253.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38447568 T>C maps to NM_001254.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:105478158 C>T maps to NM_145701.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:54605768 C>T maps to NM_201546.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:68862164 C>T maps to NM_004360.3 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:83378486 T>C maps to ENST00000268613 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:83636135 G>A maps to ENST00000268613 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:89260194 G>A maps to NM_004933.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr5:19571925 T>A maps to NM_004934.3 K339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr18:64176385 C>T maps to NM_021153.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr18:25583074 C>T maps to NM_001792.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73377068 C>T maps to ENST00000398860 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73551087 G>A maps to ENST00000398860 P2088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73553176 C>T maps to ENST00000398860 I2169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73574947 C>T maps to ENST00000398860 N3331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:73492026 G>A maps to ENST00000398860 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:23523352 G>T maps to NM_022478.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr20:58587640 C>T maps to NM_177980.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr16:68716272 C>T maps to NM_001793.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr16:66423378 G>A maps to NM_001795.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr16:66423408 C>T maps to NM_001795.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:31294253 C>T maps to NM_004932.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr18:63527020 T>C maps to NM_004361.2 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:61935329 T>C maps to NM_001796.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:26885963 T>G maps to NM_016279.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:26885963 T>G maps to NM_016279.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:85958846 C>T maps to NM_033100.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:105621473 C>T maps to NM_152750.4 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:105636764 C>T maps to NM_152750.4 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr16:29870829 G>T maps to NM_006319.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:1647900 C>T maps to NM_024011.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:37619037 G>A maps to NM_016507.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:37627386 A>G maps to NM_016507.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:123749833 G>A maps to NM_004642.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:30815207 G>A maps to NM_003885.2 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:219824730 G>C maps to NM_003936.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:219824730 G>C maps to NM_003936.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:92462571 G>A maps to NM_001145306.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:133655066 C>T maps to NM_001113575.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:39440540 G>A maps to ENST00000395035 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:18664127 C>T did not map to a codon.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr23:18671624 C>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:133747353 C>G maps to NM_080656.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:125873795 C>T did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:15519028 A>C maps to ENST00000455584 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:88874544 G>T maps to NM_030928.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:4892380 C>T maps to ENST00000328908 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:80642075 C>T maps to NM_152342.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:42092224 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:42125708 G>A maps to NM_001817.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43093717 C>T maps to NM_001816.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43093792 G>A maps to NM_001816.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:37454997 A>G maps to NM_005760.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:37455231 C>A maps to NM_005760.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:135942007 C>T maps to NM_001807.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr12:51736399 G>A maps to NM_001971.5 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:46760101 C>T maps to NM_014246.1 T2942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:46761134 G>T maps to NM_014246.1 T2849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:46859700 C>T maps to NM_014246.1 T1362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:46761564 G>C maps to NM_014246.1 L2774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:46762359 G>A maps to NM_014246.1 N2741N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:48699133 G>T maps to NM_001407.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:3766884 G>A maps to NM_001810.5 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:25480615 T>A maps to NM_018451.3 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173772505 T>G maps to NM_001127181.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:42342461 C>T maps to NM_024053.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:117214880 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:243328225 A>G maps to NM_014812.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:243329092 G>C maps to NM_014812.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:13040857 A>G maps to NM_032142.3 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:13068190 C>A maps to NM_032142.3 G1571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34084414 G>C maps to NM_007186.3 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34089678 C>T maps to NM_007186.3 S1302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34091623 G>A maps to NM_007186.3 Q1809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr12:88483186 A>G maps to NM_025114.3 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:95262979 C>T maps to NM_018131.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:80881356 G>C did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:101477213 C>A maps to ENST00000327230 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:31918103 G>A maps to ENST00000437789 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:196648798 T>C maps to NM_000186.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:117306990 C>T maps to NM_000492.3 Y1424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:49551572 C>T maps to ENST00000448456 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:151493097 C>T maps to NM_020770.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:55005082 C>T maps to NM_006568.2 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:48543123 G>A maps to NM_001267.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:132470418 G>A maps to ENST00000448878 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:98216990 C>A maps to NM_001270.2 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:93552522 C>G maps to NM_001271.3 S1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:7796804 C>G maps to NM_001005271.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr12:6710853 G>A maps to ENST00000309577 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:6188595 G>A maps to NM_015557.2 A1231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr1:6196686 G>T maps to NM_015557.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr8:61767069 G>A maps to NM_017780.2 S2308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:21868677 C>T maps to NM_001170629.1 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:53855737 G>C maps to NM_018397.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:53855737 G>C maps to NM_018397.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr22:29130411 G>A maps to NM_001005735.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:72797295 A>T did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:902267 G>A maps to NM_001142676.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:85119696 C>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:241797790 A>G maps to NM_001821.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78972901 C>T maps to NM_024591.4 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:78968836 C>A maps to NM_024591.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:78972191 C>T maps to NM_024591.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:240072487 C>A maps to NM_000740.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr15:78894446 G>A maps to NM_000743.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:78893786 G>A maps to NM_000743.4 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:78894419 A>G maps to NM_000743.4 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:40339249 T>C maps to NM_017581.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:45671240 C>G maps to NM_003654.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:101009868 C>T maps to NM_004854.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:126260790 C>T maps to NM_152889.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:126260994 C>T maps to NM_152889.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:75564171 C>G maps to NM_024533.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:129520931 T>G maps to NM_175856.4 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr16:840178 C>T maps to ENST00000317063 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:846011 C>T maps to ENST00000317063 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:841237 G>A maps to ENST00000317063 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:57468109 G>A maps to NM_020313.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:24775286 G>A maps to NM_014430.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:24775286 G>A maps to NM_014430.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:11000861 G>T maps to NM_000246.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:120139700 T>G maps to ENST00000392521 G1789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:120260705 G>A maps to ENST00000392521 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:120222829 G>A maps to ENST00000392521 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:130938649 G>A maps to NM_012127.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:130941450 C>T maps to NM_012127.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:130948017 G>A maps to NM_012127.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:122104691 G>A maps to NM_015282.2 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:33759473 C>T maps to ENST00000359576 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:33543194 C>T maps to ENST00000359576 A1470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:87043732 C>T maps to ENST00000263723 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:109477405 C>T maps to NM_001048210.1 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:11879571 C>T maps to ENST00000376496 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:11876691 G>A maps to ENST00000376496 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:11884585 G>A maps to ENST00000376496 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:1500566 C>T maps to ENST00000382745 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:1506129 C>T maps to ENST00000382745 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:37833360 G>A maps to NM_001146077.1 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:43201613 C>T maps to NM_148960.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:8559916 G>A maps to NM_194284.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:38724042 G>A maps to NM_175060.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:11114173 A>G maps to ENST00000409790 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:11133641 G>A maps to ENST00000409790 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:11133680 C>T maps to ENST00000409790 N536N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:11097154 G>A maps to ENST00000409790 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:139225214 T>C maps to NM_001080511.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:8290880 T>C maps to NM_016184.3 *238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:71043606 G>C maps to NM_173535.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:71046535 G>A maps to NM_173535.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:7828276 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:10278005 C>A maps to NM_197947.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:141313499 G>A maps to NM_004362.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr4:141313739 C>T maps to NM_004362.2 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:139890104 C>G maps to NM_004669.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:201721688 C>T maps to NM_001162407.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:17517140 G>A maps to NM_001079827.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:140281767 G>A maps to NM_022131.2 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:36197563 A>G maps to NM_007096.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:19213090 C>T maps to NM_007098.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr22:19175132 C>A maps to NM_007098.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:27457506 G>C maps to NM_001831.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:27468004 G>A maps to NM_001831.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3554798 T>C maps to NM_015041.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:3554798 T>C maps to NM_015041.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr18:618014 C>G maps to NM_199167.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr8:62289217 C>T maps to NM_173519.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:62370915 T>G maps to NM_173519.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:108686571 C>T maps to NM_001142344.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:79029024 T>C maps to NM_153610.3 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:79028812 G>T maps to NM_153610.3 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr8:88298780 T>A maps to NM_173538.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:150912170 G>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:150908167 G>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:58001085 C>T maps to NM_001297.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:58001085 C>T maps to NM_001297.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:26508996 C>T maps to ENST00000374253 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr19:1037763 C>G maps to NM_004368.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:101120670 G>A maps to NM_020348.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:104678800 C>T maps to NM_017649.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr10:104679784 A>G maps to NM_017649.3 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr2:97483237 A>G maps to NM_017623.4 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:88854165 C>T maps to NM_016083.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr9:17135257 C>A maps to NM_017738.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:2787337 G>A maps to NM_175607.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:100226899 G>A maps to NM_014361.2 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:100211840 T>A maps to NM_014361.2 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:39149903 G>A maps to NM_033655.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:76461497 T>G did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:125627338 G>T maps to NM_130773.2 E1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr7:51203881 T>C maps to ENST00000395542 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:51093048 C>T maps to ENST00000395542 E1257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:165550999 G>A maps to ENST00000392717 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:230796532 T>G maps to NM_007357.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:230810857 T>C maps to NM_007357.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr13:46104848 C>T maps to NM_031431.2 H797H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr16:70515314 G>A maps to NM_015386.2 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:23403743 A>G maps to NM_153603.3 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:33133554 C>T maps to NM_080680.2 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:75827164 G>A maps to ENST00000322507 D2484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:71640266 C>A maps to ENST00000356340 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr8:121282319 C>A maps to NM_021110.1 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr8:121219272 A>T maps to NM_021110.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:101797678 C>G maps to NM_001855.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:32149325 C>T maps to NM_001856.3 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:32164125 C>T maps to NM_001856.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:105824331 C>T maps to NM_000494.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:105836065 C>T maps to NM_000494.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46900669 C>T maps to ENST00000359759 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:48263785 G>A maps to NM_000088.3 C1299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:48269166 G>A maps to NM_000088.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr7:94041933 C>T maps to NM_000089.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:94057006 C>T maps to NM_000089.3 Y1112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr6:55988900 T>A maps to NM_030820.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:56035494 G>A maps to NM_030820.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:55924957 G>A maps to NM_030820.3 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr8:139626109 C>T maps to NM_152888.1 P1326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr8:139712354 G>A maps to NM_152888.1 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:139609155 G>A maps to NM_152888.1 Q1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:86591013 T>C maps to NM_152890.5 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:116958282 G>A maps to NM_032888.2 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117068825 G>A maps to NM_032888.2 V1655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:7571419 T>C maps to NM_001037763.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:7398422 C>T maps to NM_001037763.2 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:48381393 G>A maps to NM_001844.4 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:189849576 A>G maps to NM_000090.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:189858789 T>C maps to NM_000090.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:189862994 T>C maps to NM_000090.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:111102769 C>T maps to NM_001846.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr2:228125810 C>T maps to NM_000091.4 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr2:228172582 G>A maps to NM_000091.4 G1470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:228004876 C>T maps to ENST00000396625 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr23:107923950 C>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:107867475 A>T did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:107816877 A>G did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr9:137726978 C>T maps to NM_000093.3 L1767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:137630360 G>A maps to NM_000093.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:47422173 G>A maps to NM_001848.2 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:47545888 C>G maps to NM_001849.3 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr2:238277338 G>A maps to NM_004369.3 D1589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:238253331 G>A maps to NM_004369.3 A2443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:238280552 G>A maps to NM_004369.3 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr2:238249704 G>A maps to NM_004369.3 I2618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:130188008 C>T maps to ENST00000312481 G2387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr3:130116568 G>A maps to ENST00000312481 G1237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:130287095 C>T maps to NM_001102608.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:130289686 C>T maps to NM_001102608.1 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:130380709 C>T maps to NM_001102608.1 F2020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:130311550 A>T maps to NM_001102608.1 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:36563508 G>A maps to NM_005202.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:61452555 G>A maps to NM_001853.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:3691386 C>T maps to ENST00000418971 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:19950267 G>A maps to NM_001135162.1 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:128984408 G>A maps to NM_016128.3 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:128971750 C>T maps to NM_016128.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:232653357 C>T maps to NM_022730.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:56664040 G>A maps to NM_144576.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:198334870 A>C maps to NM_025147.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr16:30198462 C>T maps to NM_007074.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:30199791 C>G maps to NM_007074.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:84651451 G>C maps to NM_021149.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:98264477 C>T maps to NM_001862.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:77158146 C>A did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr7:129916535 G>A maps to NM_001869.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:148601595 G>A maps to NM_001870.2 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr19:17081794 G>A maps to ENST00000443236 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:17062904 G>A maps to ENST00000443236 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:148545788 C>T maps to NM_001871.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:148575249 C>T maps to NM_001871.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:173317236 T>C maps to NM_030627.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:101835763 C>G maps to NM_001308.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr14:24544772 A>C maps to NM_006032.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89645359 G>A maps to NM_014427.4 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:207834048 G>C maps to NM_173077.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr2:211464274 T>C maps to NM_001122633.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:145624577 G>A maps to NM_013291.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:68529026 A>G maps to NM_001876.3 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr22:51012004 G>A maps to NM_152245.2 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:50212023 C>T maps to NM_152359.2 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:29111949 A>G maps to NM_031311.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr23:88008608 A>G did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:88009292 A>T did not map to a codon.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr10:125557597 C>T maps to NM_198148.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:8621166 G>A maps to NM_001014447.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:207669707 G>A maps to NM_000651.4 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1706479 C>G maps to NM_020825.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131860420 G>A maps to NM_000755.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:126133251 C>T maps to NM_173689.5 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:4171824 G>A maps to NM_032607.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:4159721 C>T maps to NM_032607.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:3808871 G>A maps to NM_004380.2 Q1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:9984854 C>T maps to NM_001077415.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:1389045 C>T maps to NM_175918.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:21272248 G>A maps to NM_005207.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:18710495 G>A maps to NM_004750.4 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr4:5868476 G>A maps to NM_001014809.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:5837707 C>T maps to NM_001014809.1 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:20033193 G>T maps to NM_016652.4 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:86986862 T>C maps to NM_001143935.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:99667839 A>G maps to NM_018058.4 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:21272647 A>G maps to NM_001888.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:56669798 G>A maps to NM_004077.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr1:115276719 C>A maps to NM_001130523.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:115269684 A>G maps to NM_001130523.1 Y476Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:110466775 C>T maps to NM_000757.4 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:149460543 G>A maps to NM_005211.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:149457677 G>A maps to NM_005211.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:149460552 A>G maps to NM_005211.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:149460354 G>A maps to NM_005211.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:1413299 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:36933492 G>A maps to NM_156039.3 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr8:3141792 G>A maps to NM_033225.5 D1342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:4494913 A>G maps to NM_033225.5 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:3432585 T>G maps to NM_033225.5 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:3019695 G>A maps to NM_033225.5 P1943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:34174736 A>G maps to ENST00000373381 I1136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:34052136 G>A maps to ENST00000373381 L2300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr8:114111174 C>A maps to NM_198123.1 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:113275877 C>T maps to NM_198123.1 P3284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:113662507 A>G maps to NM_198123.1 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:113668452 A>G maps to NM_198123.1 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:113841970 A>G maps to NM_198123.1 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:64592521 T>C maps to NM_022048.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:122881388 C>G maps to NM_001044723.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr20:485847 G>A maps to NM_177559.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:58201630 G>A maps to NM_001896.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr15:75980081 G>A maps to NM_001897.4 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:75982118 G>T maps to NM_001897.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:23669597 C>T maps to NM_001899.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45196135 C>A maps to NM_000100.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:120008931 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:39736692 G>T maps to ENST00000396158 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr1:85040023 C>T maps to NM_004388.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:30910829 C>T maps to NM_001330.3 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr6:132271958 T>G maps to NM_001901.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:80646659 C>T maps to ENST00000402739 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:16707681 C>T did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:16711586 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:15767035 C>A maps to NM_007272.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr11:88070756 G>A maps to NM_001814.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr1:206329026 C>T maps to ENST00000361052 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:79224731 G>A maps to NM_004390.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr11:70265879 C>T maps to NM_001184740.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr7:117368153 T>C maps to NM_033427.2 Q1348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:88780602 C>G maps to ENST00000378384 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr10:16967408 A>G maps to NM_001081.3 P2159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:225365108 T>A maps to NM_003590.3 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:107943123 T>C maps to NM_003478.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:107965638 G>A maps to NM_003478.3 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:43006686 G>A maps to NM_001168370.1 R1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43152365 C>A maps to ENST00000354495 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43154063 C>T maps to ENST00000354495 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:43152365 C>A maps to ENST00000354495 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr7:101892120 G>A maps to ENST00000360264 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:36963225 G>T maps to NM_017748.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr17:36971289 G>A maps to NM_017748.3 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:101995476 T>G maps to NM_018294.4 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:107224414 A>G maps to NM_152434.2 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:107309825 C>T maps to NM_152434.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr4:48990494 A>G maps to NM_025087.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:218999797 T>C maps to NM_001168298.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:219000192 A>G maps to NM_001168298.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:118764381 G>T maps to NM_001716.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:118764447 C>T maps to NM_001716.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:118765107 G>A maps to NM_001716.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:237489797 C>A maps to NM_020311.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:47809709 A>G maps to NM_001101654.1 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:47813156 C>A maps to NM_001101654.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:35969412 T>C did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:35970006 A>T did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:75395308 T>C did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:75394783 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:37850384 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:45011017 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:45059837 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:40496353 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:105883825 T>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:23933911 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70325880 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:61513508 C>T maps to NM_001915.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:43024248 T>C maps to NM_001171660.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:88713212 C>G maps to NM_000101.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:37663372 A>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:37663233 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:156742032 C>T maps to ENST00000442283 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:156741410 C>T maps to ENST00000442283 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:83128910 G>C did not map to a codon.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:83127995 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:50783695 C>T maps to ENST00000311559 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:143958290 C>T maps to ENST00000377675 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:38301802 C>G maps to NM_000104.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:94835623 C>T maps to NM_000783.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr10:94824262 G>T maps to NM_183374.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:219674481 G>A maps to NM_000784.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:127956963 G>A maps to NM_001001665.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:41351210 G>A maps to NM_000762.5 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:41382543 G>A maps to NM_000764.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:41703792 G>A maps to ENST00000301173 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:99358594 C>T maps to NM_017460.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:99358597 G>A maps to NM_017460.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:99358603 T>C maps to NM_017460.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:99262834 C>T maps to NM_000777.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:99261642 A>T maps to NM_000777.3 L249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:99317992 G>A maps to ENST00000292414 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:47283813 T>C maps to NM_001099772.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16024604 C>G maps to NM_021187.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15791211 A>C maps to NM_023944.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15793237 C>T maps to NM_023944.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15793281 A>G maps to NM_023944.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15794410 C>T maps to NM_023944.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15794422 C>T maps to NM_023944.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15795938 A>G maps to NM_023944.2 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr19:15794329 C>A maps to NM_023944.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:15760034 C>G maps to NM_000896.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:59409212 C>T maps to NM_000780.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:48977188 C>T maps to NM_017457.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:6227340 A>G maps to ENST00000396741 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:37693631 C>T maps to NM_013385.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:24761501 G>A maps to NM_015330.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr17:20107644 G>T did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr21:27945185 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:59821935 C>T maps to NM_014992.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:59792754 G>A maps to NM_014992.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr14:59797396 G>A maps to NM_014992.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:85950134 G>T did not map to a codon.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr23:85403678 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:90252965 C>T maps to NM_004938.2 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:33287809 G>A maps to NM_001350.4 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr19:1434902 C>T maps to NM_018959.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:1434901 C>G maps to NM_018959.2 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:121929931 C>T maps to NM_014618.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:136521748 G>A maps to NM_000787.3 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:45444425 G>A maps to NM_001004329.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr9:34125209 G>A maps to NM_015397.3 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:27765404 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:27766473 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:27766416 A>G did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr18:50432600 C>T maps to NM_005215.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:50976897 G>A maps to NM_005215.3 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr18:50278562 T>C maps to NM_005215.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:55038535 G>A maps to NM_053283.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:32677369 C>T maps to NM_001099434.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr11:6652557 G>A maps to NM_003737.2 I1252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:155219372 A>G maps to NM_017639.3 V1576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:155407594 C>A maps to NM_001142553.1 *710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:155158283 A>C maps to NM_017639.3 L2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:155298431 A>G maps to NM_017639.3 Y133Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GS-A9TW-01A-11D-A382-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr13:36428728 A>G maps to NM_001195415.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:36779991 G>A maps to NM_033403.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:2102454 A>C maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:112349108 C>T maps to NM_152624.4 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:126215506 G>A maps to NM_014026.3 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:183814233 G>A maps to NM_001012732.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74593481 G>A maps to NM_004082.4 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74596320 T>C maps to NM_004082.4 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:50611750 C>T maps to NM_000790.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:20980798 G>A maps to NM_005216.4 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:162729612 C>T maps to NM_006182.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:112309229 C>T maps to NM_007204.4 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:94526811 C>T maps to NM_020414.3 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:125778304 C>T maps to NM_013264.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:135493791 G>A maps to NM_022779.7 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr23:41204801 G>T did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:41206197 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:41204445 G>C did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:41206602 G>A did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr17:61895139 T>C maps to NM_203499.1 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:74125282 T>C maps to NM_018665.2 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:19037175 G>A maps to NM_019070.4 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:62499162 C>T maps to NM_004396.3 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132628284 G>A maps to NM_175066.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:132625026 G>A maps to NM_175066.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr17:35993353 T>G maps to NM_007010.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124090654 C>T maps to NM_020936.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:169227550 T>C maps to NM_017631.5 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:169342925 G>A maps to NM_001012967.1 Y793Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:169294858 C>T maps to NM_001012967.1 G1578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:461442 C>T maps to NM_020664.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:460975 G>A maps to NM_020664.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:90032295 T>G maps to NM_207514.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:90028508 C>T maps to NM_207514.1 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:6914168 G>A maps to NM_021010.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:49989621 A>G maps to NM_001037497.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:49986787 T>A maps to NM_001037497.1 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:49986737 C>T maps to NM_001037497.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11831556 G>A maps to NM_001033018.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:100615706 G>A maps to NM_206918.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:100613196 G>A maps to NM_206918.2 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:18258285 C>T maps to NM_003472.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140221877 G>A maps to NM_015689.3 N896N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140225577 G>A maps to NM_015689.3 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140227183 C>T maps to NM_015689.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:111738588 A>T maps to NM_024901.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr8:142178187 C>T maps to NM_014957.2 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:65957716 C>G maps to ENST00000443035 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:9286514 C>T maps to NM_015213.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:69424866 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:69424318 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:69424306 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr22:19029398 G>A maps to NM_005137.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:20079073 C>T maps to NM_022720.6 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:56346890 C>T maps to NM_201554.1 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:14620535 C>A maps to NM_004080.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:42803314 G>A maps to NM_178009.2 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:137150664 T>C maps to NM_004717.2 E875E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:137263066 T>A maps to NM_004717.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr7:137206620 G>A maps to NM_004717.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74174012 G>A maps to NM_080916.1 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:72055077 G>A maps to NM_001361.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:24768219 G>T maps to NM_001136050.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:34951480 C>T maps to NM_024308.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr13:52346026 C>T maps to NM_001031719.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:24114489 G>A maps to NM_182908.4 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:24424345 G>A maps to NM_021004.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:12160867 C>T maps to NM_018706.5 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:24550579 G>A maps to NM_001358.2 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:47858525 C>T maps to NM_014681.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:154002773 G>A maps to NM_020865.2 N678N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:125438711 C>A maps to NM_032656.3 R833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:72132831 G>A maps to NM_014003.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:57652788 C>T maps to NM_024612.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:41570818 G>A maps to NM_004941.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:182827296 G>A maps to NM_001357.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:122692957 C>T maps to NM_019887.4 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:96354706 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:95572110 A>C maps to NM_177438.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:61525487 A>G maps to NM_033081.2 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:61510848 C>T maps to NM_033081.2 R2153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:61528043 G>A maps to NM_033081.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr12:51126264 G>A maps to NM_173602.2 P1309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr15:66621331 T>C maps to NM_001143688.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr2:233001288 C>T maps to NM_152383.4 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:40656723 C>T maps to NM_033510.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr11:111851575 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:65547774 C>T maps to NM_138368.3 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:107845786 T>C maps to NM_014421.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:12023867 A>G maps to ENST00000450094 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr8:12957769 C>T maps to NM_182643.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:196842830 A>G maps to NM_004087.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:83182725 G>T maps to NM_001142699.1 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr11:83770526 C>T maps to NM_001142699.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:79603422 C>T maps to NM_004747.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:79616519 G>C maps to NM_004747.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr18:3814274 T>A did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:1497730 G>A maps to ENST00000357934 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr8:1624700 G>A maps to ENST00000357934 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:101200779 T>C maps to NM_003836.5 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:101201205 C>T maps to NM_003836.5 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:96653683 G>C maps to NM_005221.5 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:124345720 G>T maps to ENST00000368915 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:32466653 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:32716109 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:32486755 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:33146261 A>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:78326766 C>T maps to NM_013391.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr19:36002411 G>A maps to NM_033317.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36002393 G>A maps to NM_033317.4 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:36002420 A>G maps to NM_033317.4 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:46273739 T>C maps to NM_001081562.1 *626W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:1056516 C>G maps to NM_181872.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:70218889 C>T maps to NM_001080449.1 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:70191969 A>G maps to NM_001080449.1 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:70178964 T>C maps to NM_001080449.1 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr3:52400533 C>T maps to ENST00000273600 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124270466 C>T maps to NM_207437.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124323010 T>C maps to NM_207437.3 G1519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124360031 C>T maps to NM_207437.3 H2613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:124366299 G>T maps to NM_207437.3 G2803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:124417972 C>T maps to NM_207437.3 N4346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:124272401 C>T maps to NM_207437.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:57469150 T>C maps to NM_178504.4 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:76447616 A>G maps to ENST00000389840 D3542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:76570923 G>A maps to ENST00000389840 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:76567707 G>A maps to ENST00000389840 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:76503584 G>C maps to ENST00000389840 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:76490893 G>A maps to ENST00000389840 Y2003Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:76488793 G>A maps to ENST00000389840 A2140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr17:76450727 G>A maps to ENST00000389840 D3396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:7701921 G>A maps to NM_020877.2 T2815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:21042390 G>A maps to NM_017539.1 N1805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:20948141 A>G maps to NM_017539.1 N3896N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:13841065 G>A maps to NM_001369.2 Y1886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:13867948 T>C maps to NM_001369.2 K1329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:13830748 A>G maps to NM_001369.2 C2006C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:13716796 A>G maps to NM_001369.2 G4236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:84752783 A>C maps to NM_001370.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:84926755 G>A maps to NM_001370.1 L2572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:196825255 G>C maps to NM_018897.2 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:196825255 G>C maps to NM_018897.2 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr2:196852947 A>G maps to NM_018897.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:38805752 G>A maps to ENST00000327475 T1455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:38903420 G>A maps to ENST00000327475 R3825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:38882999 C>T maps to ENST00000327475 S3317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11532786 C>T maps to NM_001372.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11540078 C>T maps to NM_001372.3 H588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11550412 T>C maps to NM_001372.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11583244 G>A maps to NM_001372.3 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11592927 C>T maps to NM_001372.3 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11622728 C>T maps to NM_001372.3 T1877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:11687720 G>A maps to NM_001372.3 A2642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:11502187 C>T maps to NM_001372.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:11687720 G>A maps to NM_001372.3 A2642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr17:11666906 C>T maps to NM_001372.3 F2382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr17:72287204 C>T maps to NM_023036.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:72306238 C>G maps to NM_023036.4 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr15:78565494 G>A maps to NM_018602.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:14629137 C>T maps to NM_006145.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:74098036 A>G maps to NM_017626.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:108213544 T>C maps to NM_012328.2 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr2:183627528 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:6700044 G>A maps to NM_018198.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:132166301 T>G maps to NM_015268.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:34937648 G>A maps to NM_194283.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3707261 G>A maps to NM_005223.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:2287293 C>T maps to NM_001374.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr16:2287820 G>A maps to NM_001374.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140051008 G>A maps to NM_194249.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:6559960 G>A maps to NM_144666.2 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:10870485 A>G maps to NM_001005361.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:31388079 C>T maps to NM_006892.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:128795080 G>A maps to ENST00000398025 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:225637894 C>T maps to NM_014689.2 L2061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:117680018 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:169116303 T>A maps to NM_004946.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:169469087 G>C maps to NM_004946.2 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr3:51317589 T>C maps to NM_004947.4 H959H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:51386356 C>T maps to NM_004947.4 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr8:25181468 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:25149589 G>A maps to NM_024940.6 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:25149611 C>T maps to NM_024940.6 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:11325004 C>T maps to ENST00000319867 Q1428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr1:62962114 G>T maps to ENST00000371140 G1606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:328143 G>A maps to NM_203447.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:382645 C>T maps to NM_203447.3 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:74783099 G>A maps to NM_001381.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:131708709 G>A maps to NM_014908.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr6:83849763 T>C maps to NM_015018.2 T1722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr21:37584330 C>T maps to NM_005128.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:2222326 G>A maps to ENST00000221482 A1053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:65113458 G>T maps to NM_006268.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:162876788 T>C maps to NM_001935.3 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr9:140009156 G>T maps to NM_013379.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:109049506 A>G maps to NM_018189.3 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:34978925 G>A maps to NM_015283.1 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:95746882 G>A maps to NM_181787.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr2:27147876 C>T maps to NM_020134.3 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:27163000 C>T maps to NM_020134.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:27121393 G>A maps to NM_020134.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:100509421 C>T did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:100497417 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:28710614 C>A maps to NM_024421.2 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:28712638 T>C maps to NM_024421.2 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr18:28710614 C>A maps to NM_024421.2 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr18:28662380 T>G maps to ENST00000438199 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr21:42064784 C>T maps to NM_001389.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr21:41648054 G>A maps to NM_001389.3 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:117329596 G>C maps to NM_020693.2 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:116758003 C>T maps to NM_013352.2 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr18:65180408 G>T maps to NM_032160.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr18:65178777 G>T maps to NM_032160.2 S1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:65180705 T>C maps to NM_032160.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:28934273 C>T maps to NM_001942.2 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr18:29098212 C>T maps to NM_001943.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr18:29055634 C>T maps to NM_001944.2 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:7576568 T>C maps to NM_004415.2 Y891Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr6:7584953 C>T maps to NM_004415.2 L2487L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6325-01A-11D-2210-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G8-6326-01A-11D-2210-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G8-6326-01A-11D-2210-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G8-6326-01A-11D-2210-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G8-6906-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:56505174 T>A maps to ENST00000361203 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:56327855 C>T maps to ENST00000370754 V5543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:56494070 A>G maps to ENST00000361203 N1273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:56505174 T>A maps to ENST00000361203 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:56505291 G>A maps to ENST00000361203 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:212218053 A>C maps to NM_016448.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:25611101 G>A maps to NM_021907.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:15533468 G>A maps to ENST00000515875 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr12:113496146 C>T maps to NM_004416.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr12:113496134 C>T maps to NM_004416.2 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr12:113496131 C>T maps to NM_004416.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr12:113496023 G>C maps to NM_004416.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr12:113496200 G>A maps to NM_004416.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr7:76132840 G>A maps to NM_020892.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:76109876 G>A maps to NM_020892.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:76132804 C>G maps to NM_020892.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:58949851 C>T maps to NM_015177.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:45427344 C>T maps to NM_175940.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:45444571 T>C maps to NM_175940.1 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr15:45439819 C>T maps to NM_175940.1 R838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr15:45403768 C>T maps to NM_014080.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr15:45404809 C>T maps to NM_014080.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:76797659 C>T maps to NM_001003892.1 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:221912333 T>G maps to NM_007207.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:96809899 G>C maps to NM_004418.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:96810589 G>C maps to NM_004418.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:167096794 G>A maps to NM_001080426.1 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:1580172 C>A maps to NM_004420.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:1273784 G>A maps to ENST00000378888 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr14:102476411 C>T maps to NM_001376.4 V2070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:102469272 T>C maps to NM_001376.4 Y1618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:102482398 C>T maps to NM_001376.4 I2483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:102516486 G>A maps to NM_001376.4 T4588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:103115999 T>C maps to NM_001080463.1 A3320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:40317310 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:68052165 C>T maps to NM_006482.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:71778828 G>A maps to NM_001130987.1 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:207564536 C>T maps to NM_001093730.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:67229826 C>T maps to NM_001950.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:43630155 A>C maps to NM_001159936.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:43630155 A>C maps to NM_001159936.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:43637172 G>A maps to NM_001159936.1 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:74899208 G>A maps to NM_001135752.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:183967499 A>C maps to NM_014693.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:183995838 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:11797483 A>G maps to NM_024693.4 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:150482638 C>T maps to ENST00000369049 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:150484015 G>A maps to ENST00000369049 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:95267937 T>C maps to NM_001393.3 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:11617019 T>G maps to NM_016581.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:139223634 A>T did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:69253327 G>C did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:5229642 C>T maps to NM_014674.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:83433086 G>A maps to NM_005711.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:144671954 C>T maps to NM_032378.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:3980851 G>A maps to NM_001961.3 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:28381068 A>G maps to NM_198529.3 E699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:28407860 G>A maps to NM_198529.3 K1096K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:56145109 G>T maps to NM_001039349.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr6:52344013 C>G maps to NM_018100.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:52288817 G>C maps to NM_018100.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr2:233546428 G>T maps to NM_025202.3 *240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:68058641 C>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:110884395 A>G maps to NM_001963.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:38409146 C>T maps to ENST00000354891 N430N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:55238086 C>T maps to NM_201284.1 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:55238086 C>T maps to NM_201284.1 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:55268915 C>T maps to NM_005228.3 D994D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:55238873 T>A maps to NM_005228.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:55259449 C>T maps to NM_005228.3 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:55238086 C>T maps to NM_201284.1 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:55238873 T>A maps to NM_005228.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:55268915 C>T maps to NM_005228.3 D994D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:41306770 G>A maps to NM_053046.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr5:137801552 C>T maps to NM_001964.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr10:64575714 G>A maps to NM_001136178.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:65349036 G>A maps to NM_001099409.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:65349036 G>A maps to NM_001099409.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140671146 C>T maps to NM_024757.4 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140707589 C>T maps to NM_024757.4 P1000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:31851171 G>A maps to ENST00000395728 C1044C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:150285534 T>C maps to NM_032025.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:37353463 A>G maps to NM_001135651.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:88926521 C>A maps to NM_004836.5 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:36367664 C>T maps to NM_012199.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:36521339 C>T maps to NM_024852.2 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:24073784 A>G did not map to a codon.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr10:120824952 A>C maps to NM_003750.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr7:2409104 A>C did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr8:109215228 G>A maps to NM_001568.2 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:8016898 C>G maps to ENST00000449102 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:10226685 G>A maps to NM_003755.3 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:32622232 A>T did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr3:186502429 C>T maps to ENST00000440191 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:184037522 C>T maps to NM_001194947.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:184049806 C>T maps to NM_001194947.1 D1524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:10821184 G>A maps to ENST00000429377 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr9:23762078 G>A maps to ENST00000359598 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr13:41507881 C>T maps to NM_172373.3 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:140046465 A>C maps to ENST00000379550 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:129201409 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47498399 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:96641343 G>A maps to NM_005230.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:96641451 C>T maps to NM_005230.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18561419 C>T maps to NM_006532.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18561472 G>A maps to NM_006532.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:18583656 T>C maps to NM_006532.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:45014803 G>A maps to ENST00000439931 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:45003210 C>T maps to ENST00000439931 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:11005775 C>T maps to NM_017770.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:27957437 C>T maps to NM_018091.5 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:46127998 C>T maps to NM_001193268.1 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:89220873 C>T maps to ENST00000380664 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:6906468 T>C maps to ENST00000381407 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:119305281 C>A maps to NM_004098.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:71510367 C>T maps to NM_031889.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131584648 C>T maps to NM_004435.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:48110149 G>A maps to NM_001172439.1 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:130586660 C>T maps to NM_001114753.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:77079853 A>G maps to NM_001042573.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:77075630 C>T maps to NM_001042573.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr4:111398088 G>A maps to NM_001977.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:120575111 G>A maps to NM_006209.3 N854N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr8:120631488 A>T maps to NM_006209.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr17:77709107 C>T maps to NM_178543.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr17:77704924 C>T maps to NM_178543.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:97471745 G>A maps to NM_001098175.1 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:74444008 G>A maps to NM_001249.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:27758755 G>A maps to ENST00000449599 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:41542752 A>G maps to NM_001429.3 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:132504638 C>T maps to ENST00000333577 T1477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:132528723 C>T maps to ENST00000333577 D2187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:132498341 G>A maps to ENST00000333577 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:29391504 G>A maps to NM_001166005.1 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34782155 G>A maps to NM_012156.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:131186717 T>A maps to NM_001431.3 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:111531386 A>T maps to NM_022140.3 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:112017882 A>G maps to NM_019114.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr2:120799655 T>G maps to NM_020909.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:143088591 G>A maps to NM_005232.4 H963H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:16458338 G>A maps to NM_004431.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr3:89390950 C>T maps to NM_005233.5 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:89391214 G>A maps to NM_005233.5 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:222301159 G>T maps to NM_004438.3 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:93982099 C>T maps to NM_004440.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:23222007 C>T maps to ENST00000400191 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:184290806 G>A maps to NM_004443.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr7:100420196 C>T maps to NM_004444.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:142562010 C>T maps to NM_004445.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:142561785 T>C maps to NM_004445.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:226032895 T>C maps to NM_001136018.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:27358508 A>G maps to ENST00000458037 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:37033347 A>G maps to NM_014805.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:144942096 G>A maps to NM_031308.1 H1775H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:144942933 C>T maps to NM_031308.1 A1496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:144941939 G>A maps to NM_031308.1 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:144943383 G>A maps to NM_031308.1 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:144945534 G>A maps to NM_031308.1 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:144947061 C>T maps to NM_031308.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr8:144942990 G>A maps to NM_031308.1 Y1477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:51829574 C>T maps to NM_001981.2 K774K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:51869183 T>G maps to NM_001981.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:15776094 C>T maps to NM_004447.5 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:15776094 C>T maps to NM_004447.5 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:37863267 G>A maps to NM_004448.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr5:65349496 C>A maps to ENST00000506030 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:65350043 A>G maps to ENST00000506030 Q966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:212251863 T>C maps to NM_005235.2 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:212587118 T>C maps to NM_005235.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:212251863 T>C maps to NM_005235.2 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:56026203 C>T maps to ENST00000460849 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:14031694 A>G maps to NM_005236.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:103514938 C>T maps to NM_000123.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:103518035 A>G maps to NM_000123.2 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:103519118 G>A maps to NM_000123.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:50678543 A>C maps to NM_000124.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:71426261 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr12:29514612 T>C maps to NM_016570.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:5805740 C>T maps to NM_024896.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:62149422 G>A maps to NM_001433.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:62132159 C>T maps to NM_001433.3 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:53133133 A>G maps to NM_014584.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:236381832 A>G maps to NM_019891.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:15070168 T>A maps to NM_152321.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:53680134 C>T maps to NM_012291.4 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:6500711 C>G maps to NM_031475.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:152201862 C>T maps to NM_001122741.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:68269819 C>T maps to NM_024939.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:64083272 C>T maps to NM_004451.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:103495006 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:138176435 A>G maps to NM_031913.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr2:67630425 G>A maps to NM_019002.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:67624738 C>A maps to NM_019002.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:159627844 T>C maps to NM_004453.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr3:185797672 G>A maps to NM_004454.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr12:11803094 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:5806511 G>A maps to NM_153717.2 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr4:5811336 A>G maps to NM_153717.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:7914021 C>T maps to NM_001159944.1 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:100563867 G>A maps to NM_016337.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:74006078 G>A maps to NM_001988.2 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:18284262 C>T maps to NM_001145127.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:176948444 C>G maps to NM_001080458.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:592565 C>T maps to NM_018303.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:67222675 G>A maps to NM_178516.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:133682284 C>T maps to NM_021807.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:133749076 C>T maps to NM_021807.3 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:231472915 G>A maps to NM_175876.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr3:38537953 G>A maps to NM_005107.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:133579151 G>A maps to NM_014285.5 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:108380608 C>T maps to NM_015065.2 R1875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:108384856 T>C maps to NM_015065.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr8:118812013 G>A maps to NM_000127.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr8:72267113 C>T maps to NM_000503.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr6:133836534 A>G maps to ENST00000452339 L532L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6325-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:65622419 G>A maps to ENST00000370616 C866C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:187195372 C>T maps to NM_000128.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:46751058 G>A maps to NM_000506.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:154221376 A>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:138643938 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:46876487 G>C maps to NM_001441.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:46871745 G>A maps to NM_001441.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr23:57515298 G>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:82370893 T>C maps to NM_001080526.1 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:70049751 C>T maps to NM_003824.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:175919323 G>A maps to NM_014613.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr5:175913490 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:80460420 C>T maps to NM_000137.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:97749729 G>T maps to NM_199336.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr3:138341027 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr17:74262007 C>T maps to NM_182565.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr9:130742407 G>A maps to NM_001035254.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:130710488 G>A maps to NM_001035254.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:55187410 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:825578 G>A maps to NM_031424.4 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:47629178 G>T maps to NM_138371.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:38907221 A>G maps to NM_138389.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50752257 G>A maps to NM_001001794.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:50753262 G>A maps to NM_001001794.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr22:50755781 G>A maps to NM_001001794.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr17:47799868 G>A maps to NM_030802.3 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr22:45719124 C>T maps to NM_017911.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr11:126110773 A>G maps to NM_024556.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:170704590 G>A maps to NM_032448.1 Q872Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:54209067 C>T did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:63411916 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:63410109 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:63412689 A>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:63412986 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:63412762 C>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:23030691 C>T maps to NM_032581.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:130270781 G>A maps to NM_022833.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:130270781 G>A maps to NM_022833.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:17643124 C>T maps to ENST00000335393 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:220046154 C>T maps to NM_024293.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:71245977 G>A maps to NM_001162529.1 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:71248045 A>G maps to NM_001162529.1 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:71195891 A>G maps to NM_020819.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:139160925 A>G maps to NM_015912.3 F1095F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:70528091 G>A maps to ENST00000430566 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:89950629 C>G maps to NM_014883.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:287645 G>T maps to NM_001002919.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:55075333 G>A maps to NM_176782.2 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:79797689 G>A maps to NM_205548.1 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:21954016 C>T maps to NM_022749.5 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:62053676 A>G maps to ENST00000404929 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr21:35757786 C>T maps to NM_058182.4 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:35757786 C>T maps to NM_058182.4 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140140187 G>A maps to NM_001001710.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:140139105 G>A maps to NM_001001710.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:93159970 T>C maps to NM_032042.5 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:102716221 A>G maps to NM_001136123.1 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:29225462 C>T maps to NM_199280.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:45431635 C>T maps to ENST00000361462 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:45473264 G>A maps to ENST00000361462 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:30818127 A>G maps to NM_032222.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:30868351 C>T maps to NM_032222.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr4:92519731 C>T maps to NM_001145065.1 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:91230406 T>C maps to NM_001145065.1 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr4:159092158 G>T maps to NM_001128424.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:68782298 C>T maps to NM_182522.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:99701001 C>T maps to NM_001170741.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr3:194408349 G>A maps to NM_153690.4 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:118166194 C>T maps to NM_017709.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:34148960 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:34961478 C>T did not map to a codon.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr23:34961270 C>T did not map to a codon.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr23:37028313 C>T did not map to a codon.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr23:37028924 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:37028761 C>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:24329792 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:153674050 A>G did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:126370637 G>A maps to NM_014661.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:136560947 G>A maps to NM_138419.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:101540551 G>T maps to NM_145037.2 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:114453548 G>A maps to NM_001077639.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr18:29850211 G>A maps to ENST00000269209 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr1:190423954 T>C maps to NM_199051.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:24843182 A>G maps to NM_014722.2 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:114507955 G>A maps to NM_182614.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:49107038 G>T maps to NM_017708.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr17:18907060 G>A maps to NM_001039999.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:5141836 C>T maps to NM_201400.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:8377347 T>C maps to NM_018088.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:33820634 C>T maps to ENST00000395190 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:8764369 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:8763297 C>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89839751 C>T maps to NM_000135.2 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89857879 C>T maps to NM_000135.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr16:89880940 A>T maps to NM_000135.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr3:10094084 T>G maps to NM_033084.3 Y520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:89849412 C>A maps to NM_001113378.1 A1175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr14:45624649 A>T maps to NM_020937.2 K462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:45665433 A>G maps to NM_020937.2 P1800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:13743324 A>G maps to NM_032228.5 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:13041557 G>A maps to NM_004461.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr2:223504316 A>T maps to NM_005687.3 L146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr10:90773124 G>C did not map to a codon.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr10:90770573 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:172628487 G>A maps to NM_000639.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:80044213 G>A maps to NM_004104.4 S1216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170403105 G>A maps to NM_024622.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170428197 G>A maps to NM_024622.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:170403105 G>A maps to NM_024622.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:207632127 C>T maps to NM_014929.3 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:7867026 A>G maps to NM_024091.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:7867026 A>G maps to NM_024091.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:187518873 G>A maps to ENST00000260147 G4113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:187629136 A>G maps to ENST00000260147 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:187541970 G>A maps to ENST00000260147 I1926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:187629136 A>G maps to ENST00000260147 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr4:187549437 C>T maps to ENST00000260147 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr4:187530475 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:150946443 G>A maps to NM_001447.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:150901208 G>T maps to NM_001447.2 R3649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:150930204 C>T maps to NM_001447.2 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:150947127 G>A maps to NM_001447.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:92577818 C>T maps to ENST00000298047 H3762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:92495107 C>G maps to ENST00000298047 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:92538350 C>T maps to ENST00000298047 L2977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:92538421 C>T maps to ENST00000298047 L3000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:92568195 C>T maps to ENST00000298047 D3344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:92616005 C>T maps to ENST00000298047 Y4128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:92624275 G>A maps to ENST00000298047 V4589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:92088523 C>T maps to ENST00000298047 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr11:92577431 G>C maps to ENST00000298047 V3633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr4:126239317 G>A maps to NM_024582.4 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr4:126408516 A>G maps to NM_024582.4 V4278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:126241564 C>T maps to NM_024582.4 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr4:126336501 C>T maps to NM_024582.4 D2128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr4:126240716 C>T maps to NM_024582.4 Q1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:73913826 G>T maps to ENST00000389570 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:73914039 C>T maps to ENST00000389570 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:40329746 C>T maps to NM_001436.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:16091699 G>A maps to NM_017556.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr15:48779515 C>T maps to NM_000138.4 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:127670411 T>G maps to NM_001999.3 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:127595152 G>C maps to NM_001999.3 L2911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:8137051 G>A maps to NM_032447.3 P2656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:8150352 C>T maps to NM_032447.3 G2327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:8150427 G>A maps to NM_032447.3 A2302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:8171067 G>A maps to NM_032447.3 C1579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:99374435 T>C maps to NM_012160.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:48059538 A>G maps to NM_001190274.1 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:28321152 A>G maps to NM_172366.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:5948351 G>A maps to NM_032807.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:39870593 T>C maps to NM_203301.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr14:55817617 T>G maps to NM_152231.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:6684002 C>G maps to NM_153230.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:16577947 G>A maps to NM_018994.1 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:16641796 C>T maps to NM_018994.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr5:171305088 T>A maps to NM_012300.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:139836693 C>T maps to NM_018998.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12805524 G>C maps to ENST00000380339 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12807065 G>C maps to ENST00000380339 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:207140993 T>C maps to NM_001170631.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr1:161187858 C>A maps to NM_004106.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:40364010 G>A maps to NM_003890.2 S4877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:161518232 C>A maps to NM_000569.6 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50017190 G>T maps to NM_004107.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr19:17897427 C>T maps to NM_015122.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:141030639 C>T maps to ENST00000354789 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:157771978 C>T maps to NM_052938.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:157736672 C>T maps to NM_030764.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr1:157670255 C>T maps to NM_052939.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr1:157665374 G>A maps to NM_052939.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr1:157516958 G>A maps to NM_031281.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:157514684 G>A maps to NM_031281.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:161680616 G>A maps to NM_001184866.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:161695617 G>A maps to NM_001002901.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:161697067 C>T maps to NM_001002901.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:155288030 C>T maps to NM_001135821.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:108294978 T>C maps to NM_005246.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:108294978 T>C maps to NM_005246.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:6078245 C>T maps to NM_017671.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:91434276 C>T maps to NM_002005.3 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:91436964 C>T maps to NM_002005.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:36818108 T>C maps to NM_001042548.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:95766335 C>T maps to NM_033086.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:95768395 C>T maps to NM_033086.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr12:32734983 A>G maps to NM_139241.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:14860967 G>A maps to NM_152536.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:76709749 C>T did not map to a codon.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr11:69625282 G>A maps to NM_005247.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:69588797 A>G maps to NM_002007.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:123239111 G>A maps to NM_001144915.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:123239111 G>A maps to NM_001144915.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:123239111 G>A maps to NM_001144915.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:123279642 C>T maps to ENST00000351936 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:123325033 C>T maps to ENST00000351936 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:1803250 T>C maps to NM_000142.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:1801510 C>T maps to NM_000142.4 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:155526108 G>T maps to ENST00000407946 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr1:60223664 G>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:17731875 A>G maps to NM_201552.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:241663824 G>A maps to NM_000143.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:241676971 G>A maps to NM_000143.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:153886103 G>A maps to NM_033393.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:153886103 G>A maps to NM_033393.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr4:153875425 A>G maps to NM_033393.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:60522656 A>C maps to NM_002012.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:106002853 G>A maps to ENST00000344213 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:67266064 T>C maps to NM_013241.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr18:34340707 C>T maps to NM_025135.2 P1346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:54324913 C>T maps to NM_030917.3 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr17:39974645 C>T maps to NM_021939.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:49315820 T>C maps to NM_016594.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:30054491 C>T maps to NM_017946.2 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:35544941 G>A maps to NM_001145775.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:35544941 G>A maps to NM_001145775.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr7:33014896 G>A maps to NM_007270.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32096527 G>A maps to NM_022110.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:152278748 T>G maps to NM_002016.1 S2871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152285540 T>C maps to NM_002016.1 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:152283266 T>A maps to NM_002016.1 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:152283604 C>A maps to NM_002016.1 G1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr1:152280083 G>A maps to NM_002016.1 S2426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152324396 G>A maps to NM_001014342.2 H1955H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152325455 G>A maps to NM_001014342.2 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:18148943 C>G maps to NM_002018.2 V1178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:18156956 G>A maps to NM_002018.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:84605343 G>A maps to NM_001001670.2 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:84609248 A>T maps to NM_001001670.2 P1288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:153578208 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:153581213 C>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:153594931 T>G did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:153594534 G>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:58080638 C>T maps to NM_001164317.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr7:128492880 G>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr13:28623524 G>A maps to NM_004119.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49977928 A>G maps to NM_001459.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:180043438 G>A maps to NM_182925.4 D1049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:180058719 G>A maps to NM_182925.4 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:33359092 T>C maps to NM_001103184.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:240371408 G>T maps to ENST00000406993 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:240371501 C>T maps to ENST00000406993 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:240371408 G>T maps to ENST00000406993 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:240635708 G>T maps to ENST00000406993 G1843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:171249932 C>T maps to NM_002021.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:171176878 G>A maps to NM_001460.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:146656088 C>T maps to NM_001144829.1 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:146993714 G>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:146993714 G>T did not map to a codon.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr2:216257690 G>A maps to NM_212482.1 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr2:216257885 G>T maps to NM_212482.1 T1279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:80684842 G>A maps to NM_024619.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:80676895 C>T maps to NM_024619.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:159647583 G>A maps to NM_032532.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:171969311 G>C maps to NM_022763.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:172061987 C>T maps to NM_022763.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr3:172025173 C>T maps to NM_022763.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr4:159789386 C>T maps to ENST00000379346 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr8:42940406 A>T maps to NM_002027.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr20:22562835 C>T maps to NM_021784.4 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr15:60297266 G>A maps to NM_012182.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr9:79635700 G>A maps to NM_001013735.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:1610820 C>G maps to NM_001453.2 Y47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:1611084 C>T maps to NM_001453.2 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:1612242 T>G maps to NM_001453.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117636 G>A maps to NM_207305.3 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:80543900 C>T maps to NM_004514.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:80545020 G>A maps to NM_004514.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:48573874 A>G maps to NM_002158.3 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:41134628 G>A maps to NM_002015.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:41240298 C>A maps to NM_002015.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:108882914 C>T maps to NM_001455.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:36886177 A>G maps to NM_001102371.1 Y644Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:36886111 G>A maps to NM_001102371.1 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr22:36886231 C>G maps to NM_001102371.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:130569257 C>T maps to NM_004957.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:74670276 G>A maps to NM_003838.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr1:74670195 C>T maps to NM_003838.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr4:79399180 C>T maps to NM_025074.6 S2688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr4:79328898 C>G maps to NM_025074.6 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:79396609 G>A maps to NM_025074.6 K2567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr9:14859352 C>T maps to ENST00000380880 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:14863862 A>G maps to ENST00000380880 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:14740228 G>A maps to ENST00000380880 Y2089Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:14750209 G>T maps to ENST00000380880 V1827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr13:39262560 T>C maps to NM_207361.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:39263421 C>T maps to NM_207361.4 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:39265557 T>A maps to NM_207361.4 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr13:39261783 C>A maps to NM_207361.4 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:39263217 C>T maps to NM_207361.4 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr13:39262599 C>T maps to NM_207361.4 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:168458001 G>A maps to NM_024919.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:13779897 C>T maps to NM_018027.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr3:69237038 G>A maps to NM_015123.1 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:131212486 G>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:131212943 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:49431170 C>T maps to NM_001018071.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:12720126 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:12728587 T>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:48542670 G>A maps to NM_015030.1 N1998N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:79495889 C>T maps to NM_001077182.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr2:186671111 T>G maps to NM_173651.2 S5782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:186671504 C>G maps to NM_173651.2 L5913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:52781028 G>A maps to NM_013409.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr5:52778713 G>C maps to NM_013409.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:132535224 G>A maps to NM_015082.1 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:162680602 A>T maps to NM_020116.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:31089872 A>T did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr5:121188182 G>A maps to NM_177478.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:2275176 G>A maps to NM_013393.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:61902010 C>T maps to NM_017647.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:37426428 T>C maps to NM_015050.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:24189739 G>A maps to NM_000147.4 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:91424028 C>T maps to NM_002569.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31193947 C>T maps to NM_004960.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49253716 G>T maps to NM_000148.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:5867724 C>T maps to NM_002034.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139925458 G>A maps to NM_004479.3 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:180630499 C>T maps to NM_005087.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:7497291 G>A maps to NM_004860.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:7496410 G>A maps to NM_004860.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:46009619 C>T maps to NM_024513.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:90895943 C>T maps to NM_003505.1 H583H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:130648575 G>T maps to NM_007197.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr12:130648917 G>A maps to NM_007197.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:28413374 C>T maps to NM_017412.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78092080 G>T maps to NM_001079804.1 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:77930446 G>A maps to NM_080491.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:153925442 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:17445709 C>T maps to NM_001037814.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:17447236 C>G maps to NM_001037814.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:17472784 G>A maps to NM_001037814.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr6:29578719 G>T maps to NM_001470.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:101151191 G>A maps to NM_005458.7 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:151358332 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:47408849 C>T maps to NM_000812.3 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:26806153 G>A maps to NM_021912.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:26825544 G>A maps to NM_021912.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr15:26806090 G>A maps to NM_021912.4 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:27222265 A>G maps to NM_033223.4 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:27777750 T>C maps to NM_033223.4 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:27725916 C>T maps to NM_033223.4 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr5:170222291 G>T maps to NM_014211.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr5:170235619 G>A maps to NM_014211.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:151820128 T>C did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:151820138 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:151817741 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:171713563 C>T maps to NM_000817.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:26575276 T>C maps to NM_001134366.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:2476601 G>A maps to NM_015675.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:843535 G>A maps to NM_005255.2 H1287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr7:99757592 G>C maps to NM_024637.4 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:151791434 C>T maps to NM_022087.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:151818707 C>T maps to NM_022087.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:101594218 A>G maps to NM_024642.3 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:155102402 T>C maps to NM_052917.2 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:230391057 G>A maps to NM_004481.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:166621412 C>T maps to NM_004482.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:89917348 C>T maps to NM_003774.4 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr12:132837583 G>A maps to NM_001122636.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132681663 G>A maps to NM_001122636.1 H600H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:172735850 G>A maps to NM_001034845.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:173269736 T>C maps to NM_001034845.2 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:42644234 A>G maps to NM_198141.2 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:22770668 T>C maps to NM_005256.3 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:114526503 G>A maps to ENST00000357389 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:8100631 T>C maps to NM_001002295.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11614558 A>G maps to NM_002052.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:11606437 C>T maps to NM_002052.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:19762988 A>G maps to NM_005257.3 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:19612026 C>T maps to ENST00000404158 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:153788926 G>A maps to NM_020699.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr15:45660420 A>G maps to ENST00000432007 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr1:155207244 G>A maps to NM_001005742.2 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:81586148 G>A maps to ENST00000264326 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:136029473 C>T maps to NM_021996.4 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:136029137 G>A maps to NM_021996.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:136029644 G>T maps to NM_021996.4 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:136029137 G>A maps to NM_021996.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:136029644 G>T maps to NM_021996.4 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:89523843 G>A maps to NM_002053.2 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:89655786 T>C maps to NM_052941.4 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:89599012 G>T maps to NM_207398.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:89613279 G>A maps to NM_207398.2 D445D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-RQ-AAAT-01A-11D-A38X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:38211727 A>G maps to NM_001171690.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:111844088 G>T maps to NM_001190259.1 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr21:34132287 G>A maps to NM_016631.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:53365101 C>T maps to NM_001498.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:53387229 C>T maps to NM_001498.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:74325100 C>T maps to NM_016591.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr12:7848213 C>T maps to NM_020634.1 K37K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:153670075 A>G did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:76944177 G>A maps to ENST00000376217 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:75150970 G>A maps to NM_030792.6 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:648915 T>C maps to NM_015721.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:650370 C>T maps to NM_015721.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:649983 G>A maps to NM_015721.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr17:648462 G>C maps to NM_015721.2 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:17961320 A>G maps to NM_001130009.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:17962116 T>A maps to NM_001130009.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42985452 G>T maps to NM_002055.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:74037368 C>T maps to NM_032380.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:3640567 C>T maps to NM_145762.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr16:23521642 G>C maps to NM_015044.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr16:23498054 C>T maps to NM_015044.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:85783340 G>A maps to NM_000821.4 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:85788527 C>T maps to NM_000821.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:25010745 T>C maps to NM_005265.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:24622123 G>A maps to NM_001099781.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:23966315 T>C maps to NM_178311.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:61995188 G>A maps to NM_000515.3 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:85902478 A>T maps to ENST00000436406 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:42689035 C>T maps to NM_000163.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr3:172163204 G>A maps to NM_198407.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:100279987 G>A maps to NM_022574.4 C906C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150439553 G>A maps to ENST00000447239 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150164188 C>A maps to NM_175571.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr5:102442521 G>A maps to NM_017676.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:46177996 G>T maps to NM_000164.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:27903997 A>C maps to NM_001085454.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:147380459 G>A maps to NM_005267.4 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr1:39341673 G>A maps to NM_030772.4 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:35227040 C>T maps to NM_153212.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:35226962 C>T maps to NM_153212.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:134239759 C>T maps to NM_138342.3 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:69561180 T>C maps to NM_015554.1 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:6587175 G>A maps to NM_000170.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:121742123 G>A maps to NM_005270.4 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:121742123 G>A maps to NM_005270.4 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:121742306 C>T maps to NM_005270.4 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:121708911 C>T maps to NM_005270.4 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:42004896 G>C maps to NM_000168.5 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:151231139 C>G maps to NM_001146040.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:151208499 C>T maps to NM_001146040.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102962342 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102979183 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:102974118 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:48182858 G>A maps to NM_015711.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:48254798 T>C maps to NM_015710.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:48259786 C>T maps to NM_015710.4 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:120182458 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:220370745 G>A maps to ENST00000373917 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr14:24702482 G>T maps to ENST00000348719 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:155633816 G>T maps to NM_003875.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:2834753 T>C maps to NM_007353.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:63010493 G>A maps to NM_006572.4 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:80144098 G>A maps to NM_004297.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:79828572 A>G maps to NM_002069.5 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:57429162 C>T maps to NM_080425.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:57478806 C>T maps to NM_080425.2 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:50232261 G>T maps to NM_000172.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr7:80117973 A>C maps to NM_001102386.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:80117992 C>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:100276354 C>T maps to NM_005273.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:100273935 C>T maps to NM_005273.3 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:180665122 G>A maps to NM_006098.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:52433396 C>T maps to NM_016194.3 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:52446259 C>T maps to NM_016194.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:52433396 C>T maps to NM_016194.3 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:52446259 C>T maps to NM_016194.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:68171214 A>G maps to NM_018841.5 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:54578724 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:42930876 G>A maps to NM_018960.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr12:102158978 G>A maps to NM_024312.4 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:1411893 G>A maps to NM_032520.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr12:65153011 G>A maps to ENST00000418919 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:133358983 A>G maps to NM_005895.3 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr3:121414038 G>A maps to ENST00000393667 N1777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:32126440 G>A maps to NM_022130.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:37797466 A>G maps to NM_152413.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:55539093 G>A maps to NM_001083899.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:145138062 G>A maps to NM_003801.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:33587297 C>T maps to NM_018025.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:217793717 A>G maps to NM_018040.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:217793483 C>T maps to NM_018040.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:156565388 C>T maps to NM_015590.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:241404913 C>T maps to NM_002081.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:99773878 G>A maps to NM_152742.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:132670268 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:132730540 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:132833965 C>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr13:93879792 G>T maps to NM_005708.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr20:5559161 A>C maps to NM_019593.3 L190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr2:157407177 G>T maps to NM_000408.4 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:157367398 G>T maps to NM_000408.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:1132383 G>A maps to NM_001505.2 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:48970654 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:176573027 T>C maps to NM_005277.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:23300351 G>T maps to ENST00000435486 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:23313744 C>T maps to ENST00000435486 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr23:136112326 C>T did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:136113229 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:132854642 T>C maps to NM_001136557.1 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:46976923 G>A maps to ENST00000283297 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:26540950 G>A maps to NM_001145168.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:46846059 C>T maps to NM_015234.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr10:95335855 G>T maps to NM_181745.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:37690614 G>A maps to NM_032777.9 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:64051852 G>A maps to NM_001170726.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:72368382 C>A maps to ENST00000440684 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:1097429 G>A maps to NM_138445.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:154147335 C>T maps to NM_001038705.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr3:154139034 T>C maps to NM_001038705.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:94957070 A>T maps to NM_199243.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:145894881 G>A maps to NM_194251.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:119886100 G>A maps to NM_153002.2 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr10:25887599 C>A maps to NM_020752.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:6934803 C>T maps to NM_019858.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:128408746 C>A maps to NM_005291.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:40094430 C>T maps to NM_007223.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:36482371 A>C maps to ENST00000398597 T2361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:36487411 G>A maps to ENST00000398597 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:57389535 G>A maps to NM_007264.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr13:99948276 G>C maps to NM_004951.4 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:125447510 G>A maps to NM_153442.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:41555135 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:241569491 G>C maps to NM_001195381.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:150348669 T>A did not map to a codon.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:150348454 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:47844898 C>T maps to NM_018485.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:47844382 G>T maps to NM_018485.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:41586751 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:41586774 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:112724146 G>A maps to NM_018970.6 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:101005553 C>A maps to NM_022049.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr1:101004705 C>T maps to NM_022049.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:90079810 C>T maps to NM_032119.3 P4530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr5:90052842 C>T maps to NM_032119.3 N3935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:101912464 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:101970661 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:101970876 T>C did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:101970122 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:13103195 G>A maps to NM_018654.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:117127550 G>A maps to NM_148963.2 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:117130560 T>G maps to NM_148963.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:46998903 G>A maps to NM_014696.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr4:90170367 G>A maps to NM_198281.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:125813448 C>T maps to NM_023927.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:50672016 G>A maps to NM_005311.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:11750984 C>T maps to NM_014668.3 H946H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:10101288 C>T maps to NM_198182.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:102585964 C>T maps to NM_024915.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:102570829 G>A maps to NM_024915.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:37436754 G>A maps to NM_012203.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:153078581 A>C maps to NM_001114183.1 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:158142837 C>T maps to NM_000826.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr10:87615869 C>T maps to NM_017551.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr10:87898677 G>A maps to NM_017551.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:94137953 G>A maps to NM_001510.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:37356578 G>T maps to NM_000831.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:9862740 G>A maps to NM_000833.3 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:9857230 C>T maps to NM_000833.3 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:13717015 G>A maps to NM_000834.3 H1052H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:48908451 G>A maps to NM_000836.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:48945043 C>T maps to NM_000836.2 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:104385645 A>G maps to NM_133445.2 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:104432461 A>G maps to NM_133445.2 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:48837642 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:47422387 C>T maps to NM_004491.4 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:86479693 G>A maps to NM_000840.2 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:88338073 G>A maps to NM_001143831.2 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38122116 G>A maps to NM_178171.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:130762323 A>G maps to NM_031415.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:144641513 G>T maps to NM_024736.6 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3627618 C>T maps to NM_031965.2 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:11969984 C>T maps to NM_002094.3 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:106058939 C>T maps to NM_183239.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:144966207 T>C maps to NM_001164629.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:81686831 C>G did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:30881102 C>A maps to NM_001517.4 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr6:158613138 C>T maps to NM_207118.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:74105423 A>G maps to NM_032999.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:135546020 G>A maps to NM_012204.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:17450037 C>T maps to NM_133644.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr3:112719764 A>G maps to NM_014170.2 *285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:42141359 C>T maps to NM_000409.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:42152582 A>G maps to NM_002098.5 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:7909889 C>T maps to NM_000180.3 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:44680659 G>A maps to NM_021927.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:72971413 A>G maps to NM_001080393.1 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:45948961 C>T maps to NM_152312.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:21692209 T>C maps to NM_021957.3 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:549010 C>T maps to NM_005317.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:129267914 T>C maps to NM_153833.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:118965687 G>A maps to NM_002105.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:134670755 G>C maps to NM_138610.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr10:71835545 C>T maps to NM_018649.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:9322193 C>T maps to NM_004285.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:26505744 G>A maps to NM_000183.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1869906 G>A maps to NM_005326.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:1869939 G>A maps to NM_005326.4 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:777589 C>T maps to NM_207112.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:7920985 C>T maps to NM_017545.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr19:52222860 G>A maps to NM_001523.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:52223025 C>A maps to NM_001523.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr8:122641109 G>A maps to NM_005328.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr9:19058364 T>C maps to NM_017645.3 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr19:17166718 G>A maps to NM_033417.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:5289815 G>A maps to NM_005330.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:135358397 G>A maps to NM_001145207.1 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:135359072 G>A maps to NM_001145207.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:153223256 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:153227752 G>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:45396653 G>A maps to NM_021072.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:605092 G>A maps to NM_001194.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:608076 C>T maps to NM_001194.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:155247407 G>T maps to NM_020897.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr15:73617311 G>A maps to NM_005477.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:73617722 G>T maps to NM_005477.2 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:240003872 G>A maps to NM_006037.3 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:240111555 G>A maps to NM_006037.3 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:240078399 G>A maps to NM_006037.3 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:240036847 C>T maps to NM_006037.3 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:71571611 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:18914208 G>T maps to NM_178425.2 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:18687541 A>T maps to NM_178425.2 P390P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FA-8693-01A-11D-2397-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:83591878 T>C did not map to a codon.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr14:31819063 C>T maps to ENST00000389961 W874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:37280710 T>C maps to NM_019024.1 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr5:41054901 T>G maps to ENST00000296803 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:139488363 C>G maps to NM_016217.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr14:31626394 G>T maps to NM_015382.2 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:93260362 C>T maps to ENST00000446394 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:43506112 A>C maps to NM_015052.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:43547691 G>A maps to NM_015052.3 Q1276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr2:197092928 C>A maps to NM_020760.1 E1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:197087060 T>C maps to NM_020760.1 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:84350869 A>G maps to NM_133636.2 H775H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:185940195 A>T maps to NM_001029887.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr17:65116526 G>A maps to NM_014877.3 R1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:65199432 A>G did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:100692329 A>G maps to NM_018437.3 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:124794762 T>G maps to NM_152722.4 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:65480100 A>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:65390578 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:93844721 C>T maps to NM_001098672.1 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr15:28366536 T>C maps to NM_004667.4 V4409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:28389879 G>A maps to NM_004667.4 S3693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:28424099 C>T maps to NM_004667.4 T3032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:28420675 C>T maps to NM_004667.4 A3271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:28459091 G>A maps to NM_004667.4 D2194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:28459392 C>T maps to NM_004667.4 V2128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr4:89427001 C>T maps to NM_016323.2 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:43246455 G>A maps to NM_144608.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:91809035 T>C maps to NM_001017975.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:81388041 T>C maps to NM_000601.4 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:79658568 C>T maps to NM_004712.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr17:79663743 G>A maps to NM_004712.4 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr4:145658961 G>A maps to NM_022475.1 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:222721251 G>A maps to NM_024746.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr1:100547629 G>A maps to NM_033055.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr7:27702326 G>A maps to NM_152740.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:75221692 C>T maps to NM_005338.4 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:75187008 T>C maps to NM_005338.4 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:75171261 G>A maps to NM_005338.4 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:114514542 G>A maps to ENST00000426820 G1108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:19340927 G>A maps to NM_003325.3 H933H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:19385569 T>C maps to NM_003325.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:26017330 C>T maps to NM_005325.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:27835054 G>A maps to NM_005322.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:27835054 G>A maps to NM_005322.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:26056470 C>G maps to NM_005319.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:26234975 C>T maps to NM_005320.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:26156899 G>A maps to NM_005321.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:26156899 G>A maps to NM_005321.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:26156968 G>A maps to NM_005321.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:26124564 C>A maps to NM_003512.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr6:26124687 G>A maps to NM_003512.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:26124780 C>T maps to NM_003512.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:26124804 G>A maps to NM_003512.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:26124609 G>A maps to NM_003512.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr6:26124711 G>A maps to NM_003512.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:26199192 C>T maps to NM_021065.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:26199192 C>T maps to NM_021065.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:27101119 C>T maps to NM_021064.4 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:27805864 G>A maps to NM_003510.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:27805993 C>A maps to NM_003510.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:27833341 C>T maps to NM_003511.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:27833377 C>T maps to NM_003511.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr6:27860756 C>T maps to NM_003514.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:27860579 C>T maps to NM_003514.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:26123769 C>T maps to NM_003526.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr6:26158775 T>C maps to NM_138720.1 *127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:26158723 G>A maps to NM_138720.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:26158525 C>T maps to NM_138720.1 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr6:26216763 C>T maps to NM_003518.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr6:26216826 G>A maps to NM_003518.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:26252147 C>T maps to NM_003524.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:27100436 C>T maps to NM_021058.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:27114199 C>T maps to NM_080593.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:27775366 C>T maps to NM_003519.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr6:27775318 G>T maps to NM_003519.3 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:27806573 G>A maps to NM_003520.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr6:27861455 G>A maps to NM_003527.4 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:26031961 G>A maps to NM_003537.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr6:26197211 C>G maps to NM_003530.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:26250505 G>A maps to NM_021018.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:26271207 T>C maps to NM_003534.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:27839874 C>T maps to NM_003533.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:27858309 G>A maps to NM_003535.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:26027285 G>A maps to NM_003544.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:26104381 C>T maps to NM_003542.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:27107281 C>T maps to NM_003495.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:27799130 G>A maps to NM_003541.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr1:149857824 G>A maps to NM_003528.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:149858046 C>T maps to NM_003528.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228612933 A>G maps to NM_003493.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228612993 T>C maps to NM_003493.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:14923886 G>A maps to NM_175054.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:71142491 C>T maps to ENST00000439900 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:75107670 C>T maps to NM_000189.4 Y515Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:176309081 C>T maps to NM_002115.2 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr19:37853920 A>T maps to NM_181786.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:29911226 G>T maps to ENST00000376806 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:29911212 G>A maps to ENST00000376806 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:29911108 G>A maps to ENST00000376806 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:31324575 G>A maps to ENST00000428231 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:31239415 G>A maps to ENST00000383329 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32975895 A>G maps to NM_002119.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32976012 G>A maps to NM_002119.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:32549583 C>T maps to NM_002124.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:32497899 A>G did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:29693018 G>A maps to NM_001098479.1 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:148768129 T>C maps to NM_003071.3 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:186043898 T>C maps to NM_031935.2 N2722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:186057346 A>T maps to NM_031935.2 T3172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:185953338 G>A maps to NM_031935.2 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:31037444 T>C maps to NM_002128.4 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1079967 G>A maps to NM_012292.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1085689 G>A maps to NM_012292.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:121437113 G>A maps to NM_000545.5 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:121416621 C>G maps to NM_000545.5 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:121435341 C>T maps to NM_000545.5 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:121437113 G>A maps to NM_000545.5 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:121416621 C>G maps to NM_000545.5 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:121435341 C>T maps to NM_000545.5 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:121437113 G>A maps to NM_000545.5 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:43048367 C>T maps to ENST00000338692 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:54676629 G>A maps to NM_031157.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr12:54676987 G>T maps to NM_031157.2 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:53216665 G>A maps to NM_001011725.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:26236234 T>C maps to NM_031243.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:12907262 A>T maps to NM_001013631.1 *294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr4:83294755 G>A maps to NM_031370.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:39331197 A>T maps to ENST00000221419 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:41811705 C>T maps to NM_007040.3 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:23744843 C>T maps to NM_020834.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:23745722 G>A maps to NM_020834.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:23744843 C>T maps to NM_020834.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:30518154 C>T maps to NM_152510.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:46669729 G>T maps to NM_002147.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr17:46669810 G>A maps to NM_002147.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:46690776 A>G maps to NM_024016.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:54379609 G>C maps to NM_017409.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr12:54367691 A>T maps to NM_014212.3 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:54422478 G>A maps to NM_004503.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:176983922 G>C maps to NM_002148.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr2:176972103 C>T maps to NM_021192.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:177034129 G>A maps to NM_006898.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr2:177016723 G>A maps to NM_014621.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:176988764 C>T maps to NM_014213.3 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:72110871 G>A maps to ENST00000228226 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:100185637 T>C maps to NM_000195.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr3:148863159 A>G maps to NM_032383.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:26864576 G>C maps to NM_022081.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:18330521 A>G maps to NM_181507.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:84222207 A>G maps to NM_006665.5 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:84222207 A>G maps to NM_006665.5 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:21978733 G>A maps to NM_005144.4 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:534241 A>G maps to NM_005343.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:534241 A>G maps to NM_005343.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:534241 A>G maps to NM_005343.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49657525 G>A maps to NM_002152.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:49658344 G>A maps to NM_002152.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr3:11302021 C>A maps to NM_001098211.1 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152193048 C>T maps to NM_001009931.1 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:20840850 C>T maps to NM_022460.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:22826320 G>A maps to NM_006043.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr16:22826242 C>T maps to NM_006043.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:14248344 G>A maps to NM_006041.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:132091066 C>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:96743583 G>T maps to NM_153456.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:88278483 T>G maps to NM_016245.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:88243831 A>G maps to NM_178135.3 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:99064377 G>A maps to NM_000197.1 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:118877676 C>T maps to NM_000414.3 Y733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120057162 G>A maps to ENST00000235547 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:120056848 C>T maps to ENST00000235547 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16263945 C>T maps to NM_032855.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:102552200 A>G maps to NM_001017963.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr6:44218143 A>C maps to NM_007355.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr10:118464771 G>A maps to NM_025015.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:122931336 T>C maps to NM_006597.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:119631653 C>T maps to NM_014365.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr1:22207013 G>A maps to NM_005529.5 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr1:22182157 G>A maps to NM_005529.5 G1904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:22169925 G>A maps to NM_005529.5 H2874H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:22214039 G>A maps to NM_005529.5 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:22183831 G>A maps to NM_005529.5 S1780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:135593166 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:135593332 G>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:63257309 C>T maps to NM_000524.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr13:47409700 G>T maps to NM_000621.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr13:47409324 C>A maps to NM_000621.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr11:113848284 G>A maps to NM_001161772.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:183777327 C>T maps to NM_130770.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:124268260 G>A maps to NM_002775.4 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:3107139 C>T maps to NM_002111.6 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr21:33371235 C>T maps to NM_014586.1 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr21:33318468 C>T maps to NM_014586.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:53654401 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:71101205 A>G maps to NM_032821.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr16:70989410 G>A maps to NM_032821.2 N2060N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:43917887 C>G maps to NM_001190880.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:118925934 G>A maps to NM_001130991.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr9:95021261 G>A maps to ENST00000375660 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:10445805 C>T maps to NM_002162.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:10404587 T>C maps to NM_003259.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr21:45656993 C>T maps to ENST00000400379 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr1:23885689 G>T maps to NM_002167.3 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr8:39782768 C>T maps to NM_002164.4 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:148579704 G>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:13264329 C>T maps to NM_004907.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr14:94594297 G>A maps to NM_032036.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:18286007 G>C maps to NM_006332.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:163128882 G>A maps to NM_022168.2 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:25671870 A>G maps to NM_001145728.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:25673000 C>G maps to NM_001145728.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:21206723 G>A maps to NM_002171.1 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:21239577 C>T maps to NM_002172.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr9:21239703 G>A maps to NM_002172.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:21166422 C>T maps to NM_002175.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:21350486 G>A maps to NM_021002.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:21409438 C>T maps to NM_002170.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:34713316 T>C maps to NM_000629.2 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:137540422 C>T maps to NM_000416.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:129237965 G>A maps to NM_052985.2 R1187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:185542652 T>A maps to NM_006548.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:160469541 A>G maps to NM_000876.2 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:71522998 C>T maps to NM_144646.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:23917175 G>A maps to NM_020070.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr22:23230314 C>T maps to ENST00000410090 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr22:23230403 A>G maps to ENST00000410090 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr22:23230347 C>T maps to ENST00000410090 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr22:23230277 G>A maps to ENST00000410090 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr22:23230379 C>T maps to ENST00000410090 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr22:23230314 C>T maps to ENST00000410090 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:23230347 C>T maps to ENST00000410090 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:23230364 A>T maps to ENST00000410090 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr22:23230277 G>A maps to ENST00000410090 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr22:23230278 C>T maps to ENST00000410090 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr22:23230347 C>T maps to ENST00000410090 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr22:23230385 C>T maps to ENST00000410090 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr22:23230418 C>T maps to ENST00000410090 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr22:23230439 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr22:23235998 G>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:23230311 C>T maps to ENST00000410090 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:23230316 G>A maps to ENST00000410090 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:23230418 C>T maps to ENST00000410090 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:23230311 C>T maps to ENST00000410090 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:23230439 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:23230403 A>C maps to ENST00000410090 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr22:23230439 G>C did not map to a codon.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr22:23230322 T>C maps to ENST00000410090 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr22:23230412 A>G maps to ENST00000410090 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr22:23230301 C>T maps to ENST00000410090 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr22:23230310 G>A maps to ENST00000410090 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr22:23230325 G>A maps to ENST00000410090 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr22:23230388 T>A maps to ENST00000410090 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr22:23230277 G>A maps to ENST00000410090 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:151155196 T>C maps to NM_178822.4 Q2384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:18731904 T>A maps to NM_173588.3 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:41142957 C>T maps to NM_001080444.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:133801989 G>A maps to NM_014987.1 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:99007410 C>T maps to NM_201612.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:111665214 A>C maps to NM_003640.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:42174379 G>A maps to NM_001556.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr8:42176068 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:206666600 C>A maps to NM_014002.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:50459541 T>C maps to NM_006060.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:117870256 C>T maps to NM_001558.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:117864061 A>G maps to NM_001558.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:67787285 T>C maps to NM_001559.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:117907927 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:81589339 C>T maps to NM_172217.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:9970061 C>T maps to NM_153461.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:9962633 C>T maps to NM_153461.2 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:113539223 G>A maps to NM_000575.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:102781465 A>G maps to NM_000877.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:102781628 G>A maps to NM_000877.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:102626186 G>A maps to NM_004633.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:27460435 C>T maps to NM_181079.4 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:14162739 A>G maps to NM_004843.2 K557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:24496084 G>A maps to NM_170743.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:70693990 C>T maps to NM_152456.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:1471061 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50393742 A>G maps to NM_172374.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:27356270 T>C maps to NM_000418.2 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:3139909 T>C maps to NM_000564.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:153635021 A>G maps to NM_004515.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:10795538 T>G maps to NM_153464.2 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:86385811 T>C maps to NM_006839.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:43923210 G>A maps to NM_175882.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:62455981 G>A maps to NM_176877.2 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:61897541 G>A maps to NM_001040694.1 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:6760366 C>T maps to NM_001127582.1 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr2:121107184 G>A maps to NM_002193.2 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:30795418 C>T maps to NM_006774.4 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:41277550 T>C maps to NM_017553.1 E1302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:33048616 G>A maps to NM_001098817.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:206872125 C>T maps to NM_017759.4 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:206872125 C>T maps to NM_017759.4 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr4:143235863 C>T did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr4:143044562 A>C maps to NM_003866.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:38343862 G>A maps to ENST00000373026 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:121587115 C>T maps to NM_014937.2 R1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:71949156 C>T maps to NM_001567.3 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:5233663 A>G maps to NM_002195.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr19:7174666 C>T maps to NM_000208.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:156814883 C>T maps to NM_014215.2 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:1538173 C>T maps to ENST00000389470 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:153740284 G>A maps to ENST00000428986 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:153701187 G>A maps to ENST00000428986 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr9:103054776 C>T maps to NM_014425.2 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:44422366 A>G maps to NM_014652.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:44424524 G>A maps to NM_014652.3 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:44433054 G>A maps to NM_014652.3 K894K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:24652349 G>A maps to ENST00000458132 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:9456505 T>C maps to NM_006391.2 Y700Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:201798366 C>T maps to NM_018085.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:95411815 G>A maps to NM_022755.5 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:32672878 G>A maps to NM_001160042.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:2611907 G>C maps to NM_152558.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:90976985 A>G maps to NM_003870.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:156508791 T>C maps to NM_178229.4 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:156502773 C>T maps to NM_178229.4 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:53263763 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:53263763 C>T did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:10251271 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:131825082 C>A did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:393208 C>T maps to NM_002460.3 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr6:393223 C>T maps to NM_002460.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:393328 G>A maps to NM_002460.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:85942774 A>G maps to NM_002163.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:44096771 C>T maps to NM_001007561.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:227663445 G>A maps to NM_005544.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:107977809 C>A did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:107976166 C>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:2749538 G>C maps to NM_033267.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:55362624 C>T maps to NM_024335.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr5:50683347 G>A maps to NM_002202.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:77942315 G>A maps to NM_199296.2 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18547208 G>A maps to NM_016368.4 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr19:18546465 C>T maps to NM_016368.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr20:32996579 G>A maps to ENST00000262650 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr16:47494776 C>T maps to NM_030790.3 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:2930730 C>T maps to NM_018463.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:68631919 C>T maps to ENST00000423218 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:68650912 G>A maps to ENST00000423218 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:68643658 G>A maps to ENST00000423218 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr5:52351855 T>C maps to NM_002203.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:52347390 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42455125 C>T maps to NM_000419.3 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42457086 C>T maps to NM_000419.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42457119 C>T maps to NM_000419.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:48151295 T>C maps to NM_002204.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:182322530 G>A maps to NM_000885.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:182392095 A>G maps to NM_000885.4 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:173362719 T>C maps to ENST00000264106 F1041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:37536019 C>T maps to NM_002207.2 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:37860416 C>T maps to NM_002207.2 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:37550108 A>G maps to NM_002207.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31422530 T>C maps to ENST00000444228 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31429478 T>C maps to ENST00000444228 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:30495495 C>T maps to NM_002209.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr2:187521025 A>C maps to NM_002210.3 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:187490231 G>A maps to NM_002210.3 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr2:187533625 G>A maps to NM_002210.3 E857E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31382463 G>C maps to NM_000887.3 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:31382469 A>G maps to NM_000887.3 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:46330666 G>A maps to NM_000211.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:45331301 A>G maps to NM_000212.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:7759735 G>A maps to NM_002216.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr10:7780635 C>A maps to NM_002216.2 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:52840324 C>T maps to NM_002217.3 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr10:7679230 C>T maps to ENST00000256861 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:7628026 C>T maps to ENST00000256861 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:54783951 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:54815064 G>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:54783778 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:160853311 C>T maps to NM_017625.2 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:160853311 C>T maps to NM_017625.2 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:231742137 G>A maps to NM_030926.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr1:226925147 G>A maps to NM_002221.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:226924564 C>A maps to NM_002221.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:226924769 C>T maps to NM_002221.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr1:226925102 C>T maps to NM_002221.3 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr3:4722293 C>T maps to ENST00000356617 R1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:26834832 G>A maps to NM_002223.2 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:33658779 C>T maps to ENST00000374316 A2373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr16:19126811 G>A maps to NM_001034841.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:19126577 T>C maps to NM_001034841.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr21:35190668 C>T maps to NM_003024.2 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:24498673 C>T maps to NM_006277.2 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:128244215 T>C maps to NM_017969.2 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:10624501 G>A maps to NM_000214.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr20:10633194 C>T maps to NM_000214.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105622156 G>A maps to NM_002226.3 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:105615513 G>A maps to NM_002226.3 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:65300304 T>C maps to NM_002227.2 Q1135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:5050705 C>T maps to NM_004972.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:5050705 C>T maps to NM_004972.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:5050705 C>T maps to NM_004972.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:5081779 G>A maps to NM_004972.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:6062159 C>T maps to NM_001099433.1 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr10:133962950 C>T maps to NM_001105521.2 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr11:134019042 C>T maps to NM_032801.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:15517414 C>T maps to NM_004973.2 V1158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:42139874 A>G maps to NM_005090.3 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:143746106 C>T maps to NM_003724.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:143746721 G>A maps to NM_003724.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2253640 G>T maps to NM_144616.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:23444246 G>A maps to NM_032876.4 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr6:24358061 C>T maps to NM_181337.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:8538658 A>C did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr3:124103696 G>A maps to NM_001024660.3 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:124174061 C>T maps to NM_001024660.3 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:124374486 T>C maps to NM_001024660.3 Y1944Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:123953755 C>A maps to NM_001024660.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:124201698 C>T maps to NM_001024660.3 Y1410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:124044858 C>T maps to NM_001024660.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:124157797 C>A maps to NM_001024660.3 R1036R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr3:124175524 C>T maps to NM_001024660.3 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:738502 C>T maps to NM_015158.2 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr19:11289040 C>T maps to NM_015493.6 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr17:40267788 G>A maps to NM_021078.2 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:40266532 G>A maps to NM_021078.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:40265750 C>T maps to NM_021078.2 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr13:30784565 A>G maps to NM_032116.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:41706449 G>C maps to NM_152903.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr17:7832621 C>T maps to NM_004732.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:73849767 A>C maps to NM_004770.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr11:17793669 C>T maps to NM_001112741.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr12:75436935 G>A maps to NM_139137.2 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr12:75601403 G>A maps to NM_139137.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:110766184 C>T maps to NM_004978.4 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:48826489 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:108867912 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:210857144 C>T maps to NM_172362.2 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:40312348 G>A maps to NM_012285.2 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:63174699 G>A maps to NM_139318.3 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:63175011 A>G maps to NM_139318.3 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:163228506 A>C maps to NM_033272.2 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr3:19322822 T>C did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:21319184 T>A maps to NM_021012.4 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:68128416 C>T maps to NM_018658.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr21:39087048 G>A maps to NM_002240.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr1:233802347 C>G maps to NM_002245.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:47748486 G>A maps to NM_022055.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:47748387 G>A maps to NM_022055.1 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr14:90650647 G>A maps to NM_022054.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:39284147 C>T maps to NM_032115.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:39267229 G>A maps to NM_031460.3 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18084723 C>T maps to ENST00000222249 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18084774 G>A maps to ENST00000222249 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:18104349 G>A maps to ENST00000222249 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:18096219 C>T maps to ENST00000222249 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:113698762 C>T maps to NM_021614.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:2683251 C>T maps to NM_000218.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:2869085 C>T maps to NM_000218.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:62078183 G>C maps to NM_172107.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:138651647 A>G maps to ENST00000298480 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:196303116 C>T maps to NM_198503.2 E619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:36692302 G>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:110986479 G>A maps to NM_014379.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:37458570 C>T maps to ENST00000403888 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr6:36447472 C>T maps to NM_173562.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:215759864 A>G maps to NM_016121.3 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr1:215751395 C>T maps to NM_016121.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:66094183 C>T maps to ENST00000451741 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr4:44450162 C>T maps to NM_198353.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:23395036 T>C maps to NM_001009999.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:23409673 G>A maps to NM_001009999.2 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:23409802 G>A maps to NM_001009999.2 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr12:121882312 G>A maps to ENST00000377071 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:121877738 G>A maps to ENST00000377071 H1250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr12:121881587 C>T maps to ENST00000377071 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:86709703 C>T maps to NM_001146688.1 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:86669184 C>T maps to NM_001146688.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:137766065 G>A maps to NM_016604.3 V1674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:7013873 C>T maps to NM_015061.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:94759725 C>T maps to NM_001161630.1 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:53223818 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:53230908 C>T did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr23:44942729 A>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:55956182 G>T maps to NM_002253.2 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:142640003 T>C maps to NM_000420.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:6415734 A>G maps to NM_003685.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:141313887 A>C maps to NM_014773.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:141309151 C>T maps to NM_014773.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:48511728 C>T maps to NM_001080394.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:85695297 C>T maps to NM_014615.2 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:73493216 G>A maps to ENST00000375248 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:126079866 T>C maps to ENST00000377985 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:126087350 T>G maps to ENST00000377985 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:126056087 C>T maps to ENST00000377985 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:197427514 C>T maps to NM_014687.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:197427583 G>A maps to NM_014687.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:42832682 G>A maps to NM_015349.1 Q913Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:105352909 G>A maps to ENST00000453495 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:24570150 G>A maps to NM_014809.3 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:35972374 A>T maps to NM_024874.4 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:114124353 C>A maps to NM_001080398.1 E2004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:114172437 C>T maps to NM_001080398.1 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr6:127768257 A>G maps to NM_014702.4 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:4830970 G>T maps to ENST00000450194 T1504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:4830970 G>T maps to ENST00000450194 T1504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:22680808 T>C maps to ENST00000446597 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:27709811 C>T maps to NM_015202.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:58943846 G>A maps to ENST00000354386 E997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:138379607 C>T maps to NM_014811.3 T1084T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:2604697 G>A maps to NM_015229.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:39879404 C>T maps to NM_015038.1 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:39877010 A>C maps to NM_015038.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:96985310 T>C maps to NM_015323.4 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:75552297 T>C maps to NM_015037.2 Y667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:154525445 A>C maps to NM_001131007.1 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:5461975 T>C maps to NM_015325.1 N843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:84856408 T>C maps to NM_014895.2 K1289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:84925635 A>C maps to NM_014895.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:105550564 C>T maps to NM_015275.1 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:105550564 C>T maps to NM_015275.1 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:141362557 G>T maps to NM_001080392.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:81172063 G>A maps to NM_018689.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:81217023 G>A maps to NM_018689.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr15:81188309 C>T maps to NM_018689.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:24834979 C>T maps to NM_019590.3 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:24813584 G>A maps to NM_019590.3 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:24833406 T>C maps to NM_019590.3 R1736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:70775328 G>A maps to NM_015634.3 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:109714592 C>T maps to NM_020775.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:52901886 A>G maps to NM_019600.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:52905881 G>A maps to NM_019600.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:101829069 C>T maps to NM_020802.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:232943774 C>T maps to NM_019090.2 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:30318344 C>T maps to NM_020848.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr18:59936159 A>T maps to NM_020854.3 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:100122383 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:1374768 G>A maps to NM_020894.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:7682861 C>G maps to NM_001080429.2 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr7:138602478 C>T maps to NM_001164665.1 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:118713595 G>A maps to NM_001127211.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr18:43514835 G>A maps to NM_020964.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18368523 C>T maps to NM_001145304.1 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:36856578 G>A maps to NM_001029864.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr20:36869740 G>A maps to NM_001029864.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:36842085 G>A maps to NM_001029864.1 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:20820345 A>T maps to NM_017794.3 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:233489681 G>A maps to NM_032435.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:22464809 C>T maps to NM_021174.5 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:22472472 G>A maps to NM_021174.5 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr8:22472490 T>A maps to NM_021174.5 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139698976 G>A maps to NM_001039374.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:94369246 C>T maps to NM_004523.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:200558419 C>T maps to NM_014875.2 K1013K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr20:16360312 G>A maps to NM_024704.4 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:16492162 T>C maps to NM_024704.4 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:21031009 G>A maps to NM_020816.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:21044150 G>A maps to NM_020816.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:21031117 C>T maps to NM_020816.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:72340964 G>A maps to NM_153209.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:241702598 G>A maps to ENST00000373308 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr1:10363222 C>T maps to NM_183416.3 D660D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4918121 A>G maps to NM_006612.5 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4925673 C>T maps to NM_006612.5 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:39734065 T>G maps to ENST00000395670 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:39716674 T>A maps to ENST00000395670 R1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:69714346 T>C maps to NM_138555.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:104640097 G>A maps to NM_015656.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:104640097 G>A maps to NM_015656.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:245775264 C>T maps to NM_018012.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:245772691 A>C maps to NM_018012.3 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:86518565 T>C maps to NM_017576.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr10:32307309 T>C maps to NM_004521.2 K791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:149861926 G>A maps to NM_004522.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:39607448 C>T maps to NM_145027.4 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:90192362 G>A maps to NM_198525.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:145698757 G>A maps to NM_145754.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36349720 G>A maps to NM_199180.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36351905 C>A maps to NM_199180.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:126299147 G>A maps to NM_032531.3 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:126294660 G>A maps to NM_032531.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:126294660 G>A maps to NM_032531.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:55561861 G>T maps to NM_000222.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:88912623 G>A maps to NM_000899.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr13:33635909 T>C maps to NM_004795.3 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:104143805 C>T maps to ENST00000445352 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45848945 G>A maps to NM_177417.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1854700 G>A maps to NM_031918.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:16436832 C>G maps to NM_016270.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr19:16437841 G>C maps to NM_016270.2 *356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr19:16436025 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:38696384 C>T maps to NM_016531.5 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:110249414 T>C maps to NM_004235.4 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:27950774 G>A maps to NM_020782.1 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:18807522 G>A maps to NM_152375.2 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr13:70370950 A>G maps to NM_020866.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:202863791 G>A maps to NM_021633.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:117035895 A>G did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr18:30350107 C>T maps to NM_020805.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr18:30350265 G>A maps to NM_020805.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:899823 C>T maps to NM_198317.2 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173725100 G>A maps to NM_014458.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173735377 T>C maps to NM_014458.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:6662375 G>A maps to NM_014851.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18778878 C>T maps to NM_018316.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18779727 C>T maps to NM_018316.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:18779112 C>T maps to NM_018316.1 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:136975603 G>A maps to NM_017415.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:97533192 C>A maps to NM_052904.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:97562206 G>T maps to NM_052904.3 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:21675124 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:84691255 C>T maps to NM_024731.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:23212626 A>G maps to NM_001031710.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:51582089 G>A maps to NM_022046.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr19:51466702 G>A maps to NM_001012964.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:48687053 A>C maps to NM_001135629.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr12:10560926 C>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:123107091 G>A maps to NM_014708.4 K2151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:45734284 T>C maps to NM_002265.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr1:152732766 C>T maps to NM_001025231.1 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:47978738 C>T maps to NM_007059.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:25362776 A>G maps to NM_004985.3 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:25362776 A>G maps to NM_004985.3 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr16:3014556 C>T maps to NM_172229.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr17:39661358 A>G maps to NM_153490.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39741279 A>G maps to NM_000526.4 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39767946 C>T maps to NM_005557.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr17:39775872 G>A maps to NM_000422.2 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:39777894 T>A maps to NM_000422.2 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:38859552 G>T maps to NM_019016.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38859663 G>A maps to NM_019016.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:38927461 G>A maps to NM_181539.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr12:53185489 C>T maps to ENST00000309505 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39551532 G>A maps to ENST00000393998 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39521516 C>T maps to ENST00000394004 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39521751 G>A maps to ENST00000394004 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52865923 G>A maps to NM_173086.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52636842 G>A maps to NM_005556.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:52636918 C>T maps to NM_005556.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:52946423 G>A maps to NM_033448.2 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:52966367 C>T maps to NM_175053.3 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:53090180 G>A maps to NM_175078.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr12:53216987 C>T maps to NM_175834.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:52579314 C>T maps to NM_182507.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:52777465 C>A maps to NM_033045.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:39727893 A>G maps to NM_000226.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:39197484 A>G maps to NM_030967.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:39197172 A>G maps to NM_030967.2 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46057342 C>A maps to NM_181688.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46057942 C>T maps to NM_181688.1 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46057948 C>T maps to NM_181688.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46057951 C>A maps to NM_181688.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:46057633 T>C maps to NM_181688.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr21:46067103 C>T maps to NM_198692.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:46067193 C>T maps to NM_198692.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46117745 C>T maps to NM_198699.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr21:45970771 A>G maps to NM_198693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45978127 G>A maps to NM_198696.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45994762 C>T maps to NM_198687.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011405 G>T maps to NM_198688.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011408 G>A maps to NM_198688.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011414 G>A maps to NM_198688.2 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011543 G>C maps to NM_198688.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011546 G>A maps to NM_198688.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46011570 G>T maps to NM_198688.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:31797918 G>A maps to NM_181622.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr21:31797918 G>A maps to NM_181622.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:31802628 C>T maps to NM_181600.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr21:31802628 C>T maps to NM_181600.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:31874240 G>T maps to NM_181611.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr21:32127678 G>A maps to NM_181619.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr21:31692281 G>T maps to NM_203405.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:31709722 A>C maps to NM_001077711.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39156084 G>T maps to NM_031959.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:39274171 G>T maps to NM_033059.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr17:39274171 G>T maps to NM_033059.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39324253 G>A maps to NM_033187.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39324409 G>A maps to NM_033187.1 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39240610 G>A maps to ENST00000377731 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:39240790 C>G maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39253796 G>A maps to NM_031960.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39254183 T>C maps to NM_031960.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:39261792 G>A maps to NM_001146041.1 R51R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FA-A6HN-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr11:1651378 G>A maps to NM_001001480.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:71249529 T>C maps to NM_021046.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:71259708 C>T maps to NM_005553.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:71259840 C>T maps to NM_005553.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr14:56105907 C>T maps to NM_001079521.1 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr14:56079009 C>T maps to NM_001079521.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:134322876 G>A maps to NM_178554.4 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:134369766 G>A maps to NM_178554.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:153128161 A>G did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr18:6138190 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr19:55014154 T>C maps to NM_002288.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:48961800 C>A did not map to a codon.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr18:6978309 C>T maps to NM_005559.2 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:6961949 T>C maps to NM_005559.2 L2482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:6966295 G>A maps to NM_005559.2 S2300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr6:129636793 A>G maps to NM_000426.3 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr18:21492733 C>T maps to ENST00000416669 D2408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr18:21496532 C>T maps to ENST00000416669 D2601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr18:21453037 C>T maps to NM_000227.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:21496532 C>T maps to ENST00000416669 D2601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:112513024 G>A maps to NM_001105206.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr20:60885314 G>A maps to NM_005560.3 P3551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:60884472 C>T maps to NM_005560.3 A3669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:60885977 G>T maps to NM_005560.3 R3421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:60898653 G>A maps to NM_005560.3 N1974N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:60898890 C>T maps to NM_005560.3 L1930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:107591719 G>A maps to NM_002291.2 C1114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:49161003 C>A maps to NM_002292.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:107706207 C>T maps to NM_007356.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:107746264 T>C maps to NM_007356.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:119576454 G>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:119576454 G>A did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:37431668 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:34000459 G>A maps to NM_133642.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr4:129035898 T>C did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:909710 A>G maps to NM_015155.1 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:71128690 G>A maps to NM_018357.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:145522991 C>T maps to NM_020117.9 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:45459029 C>T maps to NM_015340.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:30480465 G>A maps to NM_030915.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:225603028 T>C maps to NM_194442.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:80223258 T>G maps to NM_181714.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152777873 T>A maps to NM_178351.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152777876 G>A maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:152552310 G>A maps to NM_032563.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139657899 C>G maps to NM_203347.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr9:139651500 A>C maps to ENST00000371689 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:139879195 C>T maps to NM_207510.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:88466464 C>T maps to NM_007078.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:54480032 G>A maps to NM_001010978.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:140271024 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:226074435 G>C maps to NM_020997.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr1:226127478 G>A maps to NM_003240.3 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:65564344 G>T maps to NM_014319.4 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:66102616 A>G maps to NM_002303.5 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:40195182 C>T maps to NM_020129.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr10:95552601 C>A maps to NM_005097.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:25014047 G>A maps to NM_018176.3 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:22009052 G>A maps to NM_139278.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:22006122 G>A maps to NM_139278.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr14:93171021 G>A maps to NM_005606.6 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:93172902 C>T maps to NM_005606.6 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:40175310 G>A maps to NM_005780.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:77784809 A>C maps to NM_005779.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr12:113901351 G>A maps to NM_022363.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:38510767 T>C maps to NM_002310.5 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:38510602 G>A maps to NM_002310.5 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:48626235 A>G maps to NM_000234.1 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:108862809 G>A maps to NM_001098268.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:54744770 A>G maps to ENST00000245620 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:54783835 G>A maps to ENST00000391747 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:50571068 G>A maps to NM_001113546.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr3:45636655 C>T maps to NM_014240.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:61775956 C>T maps to NM_030576.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:61776163 C>T maps to NM_030576.3 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr2:109300339 G>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:77907657 C>T maps to NM_032808.5 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:42910415 C>T maps to NM_005357.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:47088740 C>T maps to NM_006033.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:73559452 C>T maps to NM_001031803.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:73569210 C>T maps to NM_001031803.1 Y859Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:57026449 G>C maps to NM_005570.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:49498634 G>T maps to NM_018113.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr5:126113529 C>T maps to NM_005573.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2432449 C>G maps to NM_032737.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr13:76370886 T>C did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:76370782 A>G maps to ENST00000357063 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:69168746 A>G maps to NM_198271.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:97822989 G>A maps to NM_014916.3 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:49013808 G>T maps to NM_001080434.1 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:28130472 G>A maps to NM_153371.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:100911979 C>T maps to NM_198461.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:118109490 G>A did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr2:74761668 G>A maps to NM_032603.2 H604H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:160977166 G>T maps to NM_005577.2 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:19737991 G>A maps to NM_004720.5 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:19737991 G>A maps to NM_004720.5 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:85331461 A>C maps to NM_012152.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr16:55608566 C>T maps to NM_017839.4 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr19:14266281 G>A maps to NM_001008701.2 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr19:14288464 G>A maps to NM_001008701.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:14261852 G>A maps to NM_001008701.2 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:14288368 C>T maps to NM_001008701.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr1:82415873 G>T maps to ENST00000370717 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:188478054 C>T maps to NM_005578.3 C465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:104032337 C>T maps to NM_017753.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:99469999 G>A maps to NM_001037317.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:151388905 T>C maps to NM_006726.3 P2244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr13:47224429 C>A maps to NM_001164211.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39805187 C>T maps to NM_020862.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:40400822 C>T maps to NM_020737.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:40360491 C>T maps to NM_020737.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:133881793 T>C maps to NM_144648.1 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:133884015 C>T maps to NM_144648.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:133812350 T>C maps to NM_144648.1 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:66433457 G>A maps to NM_015541.2 C813C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:85993922 C>T maps to NM_015613.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:85982074 A>G maps to NM_001017924.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:110791452 T>C maps to NM_198506.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:57578695 C>T maps to NM_002332.2 R2087R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:57603646 C>T maps to NM_002332.2 P4145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:57594551 C>T maps to NM_002332.2 C3393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:57571248 C>T maps to NM_002332.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:57550587 G>A maps to NM_002332.2 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:57587436 T>C maps to NM_002332.2 C2591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:57579389 C>T maps to NM_002332.2 C2180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:57592066 G>A maps to NM_002332.2 T3137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:141819820 G>A maps to NM_018557.2 Y345Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:141079637 A>G maps to NM_018557.2 D4178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr2:141294278 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:141274455 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr2:141819774 G>T maps to NM_018557.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr2:170134322 C>T maps to NM_004525.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:169993976 C>T maps to NM_004525.2 G4515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170034472 G>A maps to NM_004525.2 F3411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:46914525 C>T maps to ENST00000256991 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:46918528 C>T maps to ENST00000256991 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:68193581 G>A maps to NM_002335.2 R1188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:3520700 T>C maps to NM_002337.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:3516559 G>A maps to NM_002337.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:44172495 T>C maps to NM_133259.3 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:44175292 G>A maps to NM_133259.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:145745267 G>A maps to NM_014665.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:194080173 G>A maps to NM_001135057.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:26998121 T>G maps to NM_022901.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:145748074 T>G maps to NM_001024678.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:134151130 G>T maps to NM_030626.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:62856645 G>A maps to NM_199340.2 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:40136048 A>G maps to NM_020929.1 Y598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56949528 C>T maps to NM_001005210.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr7:150034702 G>A maps to NM_023942.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:67926716 T>C maps to ENST00000421742 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:131670216 C>T maps to NM_001127244.1 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:90049087 G>A maps to NM_015350.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:90049576 C>T maps to NM_015350.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:90179469 A>G maps to NM_032270.4 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:238662004 T>C maps to NM_001137552.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr12:85459140 T>G maps to NM_001079910.1 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:74575140 G>A maps to NM_001105659.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:74649118 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:74648374 A>G maps to NM_001105659.1 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:101606083 G>A maps to NM_024652.3 A1814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:101593596 C>T maps to NM_024652.3 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:101567970 C>T maps to NM_024652.3 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:40677935 G>A did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr7:110764120 T>C maps to NM_018334.4 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:110763562 T>C maps to NM_018334.4 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:110764123 A>G maps to NM_018334.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr7:110764564 T>C maps to NM_018334.4 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:80529705 A>G maps to NM_178839.4 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:80529594 C>T maps to NM_178839.4 W450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:80529908 C>A maps to NM_178839.4 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:80529909 C>A maps to NM_178839.4 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr2:77746079 G>T maps to NM_001134745.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:130263361 C>T maps to NM_001005374.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:54958883 A>G maps to NM_020678.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:71806514 A>G maps to NM_145309.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:102106458 G>A maps to NM_152892.1 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:102112913 C>T maps to NM_152892.1 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:102113387 C>A maps to NM_152892.1 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:194371924 A>G maps to NM_018385.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18420500 G>A maps to NM_012321.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:147110789 A>T maps to NM_007080.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr21:47626601 G>A maps to NM_002340.5 N516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr12:21201644 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:31541085 C>T maps to NM_000595.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr12:96409428 C>A maps to NM_000895.1 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr6:31550122 T>C maps to NM_002341.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:31549363 G>A maps to NM_002341.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:31549603 G>A maps to NM_002341.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr6:31548737 G>A maps to NM_002341.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr2:33614281 G>C maps to ENST00000354476 V1582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:33567989 T>C maps to ENST00000354476 Y1273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:33623566 G>A maps to ENST00000354476 P1708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr14:74971791 C>T maps to NM_000428.2 A1421A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:46501307 T>C maps to NM_002343.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:46490455 G>A maps to NM_002343.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:46496909 G>A maps to NM_002343.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:139090514 A>G maps to NM_016019.2 A164A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GR-7351-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:31647043 A>G maps to NM_025262.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:143783108 A>G maps to ENST00000292430 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:160690645 T>C maps to NM_001198759.1 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:160737716 G>A maps to NM_001198759.1 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:160783594 C>T maps to ENST00000263285 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:143833839 C>G maps to NM_205545.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43967422 G>A maps to NM_014400.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:130515810 G>A maps to NM_181705.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:235971801 G>A maps to NM_000081.2 D772D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:235907278 A>G maps to NM_000081.2 I2717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:235955275 G>T maps to NM_000081.2 A1422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:235918869 T>G maps to NM_000081.2 L2379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:9995632 G>A maps to NM_032368.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:21347141 C>T maps to NM_006767.3 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:102762438 C>T maps to NM_032429.2 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:39853162 T>C maps to ENST00000361689 H2821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr20:15967420 G>A maps to ENST00000310348 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:144512156 C>T maps to NM_201589.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:79880564 G>A maps to NM_002359.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:35793378 G>A maps to NM_002361.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:151092967 G>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:151870116 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:149013962 C>T did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:27839461 A>C did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:35821007 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:30254063 C>T did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:26212457 A>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:26212333 A>C did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:140995471 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:140993884 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:140993736 C>T did not map to a codon.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr23:140995448 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:141291746 G>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:140985324 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:54837276 G>C did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:75648637 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:75649429 G>A did not map to a codon.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr3:184429558 C>T maps to NM_022149.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr15:23889330 G>A maps to NM_019066.4 R1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr3:65425590 T>C maps to NM_001033057.1 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr3:65425602 T>C maps to NM_001033057.1 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr7:79082450 C>T maps to NM_012301.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr1:114191925 A>G maps to NM_001142782.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:113933813 C>T maps to NM_001142782.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:77112934 C>T did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:149639034 C>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:91452565 G>A maps to NM_006122.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:6602377 G>A maps to NM_015274.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:6621676 C>G maps to NM_015274.1 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr15:75660457 C>T maps to NM_006715.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr4:103585913 G>A maps to NM_005908.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr6:96053986 C>T maps to NM_024641.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:38265652 T>C maps to NM_001113482.1 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:71489694 C>T maps to NM_005909.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:71495319 G>A maps to NM_005909.3 E2046E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr5:71495763 G>A maps to NM_005909.3 T2194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:17835916 C>T maps to NM_018174.4 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:66779596 A>T maps to NM_002755.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:4110551 C>G maps to NM_030662.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:4117482 G>A maps to NM_030662.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:56178614 A>C maps to NM_005921.1 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:65367222 A>G maps to NM_002419.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr12:53880794 G>A maps to NM_001193511.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:19387317 C>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:161507617 C>T maps to NM_005922.2 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:27686372 G>A maps to NM_004672.3 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:71202691 T>C maps to NM_033141.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr14:71267771 G>A maps to NM_033141.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:39101771 C>T maps to NM_001042600.1 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:36636773 G>A maps to NM_018067.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:36644873 G>A maps to NM_018067.3 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:36636773 G>A maps to NM_018067.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:20074800 C>T did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:135301795 T>C did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr4:87022298 C>T maps to NM_138982.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:86950353 A>G maps to NM_138982.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:36104467 C>G maps to NM_002754.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:19285391 G>A maps to NM_139034.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:1817854 C>T maps to NM_015133.3 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:128206854 C>T maps to NM_001006617.1 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:206905039 C>T maps to NM_032960.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr5:16091040 C>T maps to NM_001102562.1 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:103941453 G>A maps to ENST00000335102 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12978555 C>G maps to NM_014975.2 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:46496367 C>T maps to NM_015112.2 D881D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr5:66462401 C>T maps to NM_001164664.1 F2465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:66461582 C>T maps to NM_001164664.1 H2192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:27462060 G>A maps to NM_001172303.1 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:3789320 G>A maps to NM_002378.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:99028810 G>A maps to ENST00000254898 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr18:47799096 A>G maps to ENST00000424334 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr2:149226790 C>T maps to ENST00000404807 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr2:9002785 G>A maps to NM_138799.2 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:8998970 T>C maps to NM_138799.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:54682537 C>T maps to NM_024298.3 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:54687452 G>A maps to NM_024298.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:74701935 G>A maps to NM_001025101.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr17:49281176 G>A maps to ENST00000389496 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:84125393 G>A maps to NM_003791.2 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89985983 G>A maps to ENST00000304984 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89986565 C>T maps to ENST00000304984 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:150551346 C>T maps to NM_021960.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:127340582 C>T maps to NM_004526.2 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:47695219 A>G maps to NM_003906.3 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr21:47692530 T>C maps to NM_003906.3 E803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr21:47664745 C>A maps to NM_003906.3 P1671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr8:48889331 G>A maps to NM_182746.1 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:48875552 A>T maps to NM_182746.1 K216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:136602195 G>A maps to NM_005915.4 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:5943984 G>A maps to NM_032485.4 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:94858807 G>A maps to NM_018349.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:30668373 G>A maps to NM_014641.2 F2046F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:37605197 G>A maps to ENST00000297153 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:75684272 G>A maps to NM_005918.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:68708978 G>A maps to NM_017440.4 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr6:90437659 C>T maps to NM_014611.1 L1788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:90424457 C>T maps to NM_014611.1 S2291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:90500066 C>T maps to NM_014611.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70339714 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:70354253 G>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:70351981 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr23:70352366 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:150874032 T>C maps to NM_053002.4 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:151150567 G>A maps to NM_053002.4 P2138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:60038403 T>C maps to NM_005121.2 P1768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:116446354 A>G maps to NM_015335.4 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:40551992 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:20909388 G>A maps to NM_001003891.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:93529673 C>T maps to NM_004268.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:136208441 C>T maps to NM_133640.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16687869 G>A maps to NM_004831.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:17616348 G>A maps to NM_025205.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr19:39884259 C>T maps to NM_017592.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:100250917 G>A maps to ENST00000338042 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:126746146 C>T maps to NM_032446.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:3411234 G>A maps to ENST00000452816 H1389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:42873088 G>A maps to ENST00000251268 T2192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:42874899 C>T maps to ENST00000251268 C2351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr9:123367752 T>C maps to ENST00000426959 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:36597283 C>G maps to NM_014791.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr6:46766883 G>T maps to NM_005588.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr2:112779061 C>T maps to NM_006343.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:112740560 A>G maps to NM_006343.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:81294773 G>C maps to NM_022566.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:81271790 G>A maps to NM_015154.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr15:90320148 G>A maps to NM_001039958.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr15:90320148 G>A maps to NM_001039958.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr15:90320148 G>A maps to NM_001039958.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:130140728 C>T maps to NM_002402.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:116340268 C>T maps to NM_001127500.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:116339281 G>A maps to NM_001127500.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:116397571 A>G maps to NM_001127500.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:116339314 G>A maps to NM_001127500.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:116397571 A>G maps to NM_001127500.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:116339671 C>T maps to NM_001127500.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:116435767 C>T maps to NM_001127500.1 D1304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:116436021 G>A maps to NM_001127500.1 A1357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:116436096 G>A maps to NM_001127500.1 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:116339281 G>A maps to NM_001127500.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:116435767 C>T maps to NM_001127500.1 D1304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:116436021 G>A maps to NM_001127500.1 A1357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:116436096 G>A maps to NM_001127500.1 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:116397571 A>G maps to NM_001127500.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:21971693 C>G maps to NM_019852.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:2554914 G>A maps to NM_022840.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:51319237 T>C maps to NM_014033.3 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:56077598 A>T maps to NM_152637.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:170912684 T>C maps to NM_021647.6 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr4:170926947 G>A maps to NM_021647.6 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:8748057 C>T maps to NM_004225.2 K837K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:8748147 A>C maps to NM_004225.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:8749317 A>G maps to NM_004225.2 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:12061597 C>T maps to NM_014874.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr2:191300916 A>C maps to NM_017694.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:8701700 A>G maps to NM_152599.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:103343355 A>C maps to NM_032718.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr15:42003385 C>T maps to ENST00000219905 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:42019420 A>G maps to ENST00000219905 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr7:141756636 G>A maps to ENST00000475668 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:141754624 C>T maps to ENST00000475668 T1077T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:43277282 G>A maps to NM_153361.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:39717001 A>G maps to NM_054024.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:222805651 G>A maps to NM_198551.2 E1105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:31378927 C>T maps to NM_000247.1 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:18379639 C>T maps to NM_015241.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:12313844 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:1488316 G>A maps to NM_182924.3 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:1478524 C>T maps to NM_182924.3 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:107147247 A>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:97686158 C>T maps to NM_153182.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:89312045 T>C maps to NM_004897.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:56847383 G>A maps to NM_012064.3 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr3:69928320 G>A maps to ENST00000448226 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr19:2041910 G>A maps to NM_199054.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140158959 G>A maps to NM_013446.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr22:50512731 G>A maps to NM_015166.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr3:158289124 C>T maps to NM_022443.4 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr12:49427101 G>A maps to NM_003482.3 Q3796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr12:49435940 G>A maps to NM_003482.3 Q2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr12:49435032 G>A maps to NM_003482.3 Q2174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:49433355 G>A maps to NM_003482.3 R2697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:49439899 G>A maps to NM_003482.3 A1547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:49426817 G>A maps to NM_003482.3 S3890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr12:49428191 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr12:49427323 G>A maps to NM_003482.3 Q3722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr7:151896388 C>T maps to ENST00000355193 S1416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:151970898 T>C maps to ENST00000355193 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:36223698 G>T maps to NM_014727.1 T2083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr19:36218066 C>T maps to NM_014727.1 C1338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:6222551 C>T maps to NM_005934.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr17:36865738 C>T maps to NM_005937.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:36868975 G>A maps to NM_005937.3 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr1:2527446 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:24124470 C>A maps to NM_005940.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:102825226 G>A maps to NM_002427.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr16:58073911 C>T maps to NM_002428.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132329665 C>T maps to NM_016155.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:56236135 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:33855125 C>T maps to NM_006690.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:102567521 G>A maps to NM_022122.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:102593272 T>G maps to NM_002424.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:28193096 C>T maps to NM_002430.2 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:28192808 G>A maps to NM_002430.2 D1241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:93649551 A>G maps to NM_022151.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2078289 G>A maps to NM_130807.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2078423 G>T maps to NM_130807.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:33828915 A>G maps to NM_017947.2 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr20:49575720 T>C maps to NM_014484.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:29638100 T>C maps to NM_002433.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:223574545 A>G maps to NM_058165.2 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:108780894 T>A maps to NM_014429.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:106221322 C>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:13183485 T>C maps to ENST00000319217 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr11:58978340 G>A maps to NM_001039396.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr11:58978739 G>A maps to NM_001039396.1 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr11:58979543 G>A maps to NM_001039396.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr11:58980008 G>A maps to NM_001039396.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr11:58979063 G>A maps to NM_001039396.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:58978433 C>A maps to NM_001039396.1 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:71360054 C>T maps to NM_005791.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr22:43870784 C>A maps to NM_001044370.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:17030128 G>A maps to NM_015134.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:118133333 T>C maps to NM_144765.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:118134829 G>A maps to NM_144765.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:60767593 C>A maps to NM_006039.3 R1274R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G8-6906-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:18159405 C>G maps to NM_054031.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:13875452 C>T maps to NM_001031727.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:79671297 C>T maps to NM_002949.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:39421978 T>G maps to NM_033363.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:43906543 C>T maps to NM_032014.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:43908660 G>T maps to NM_032014.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:24418748 G>A maps to NM_020662.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr11:10655534 G>A maps to NM_001098579.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:60073625 G>A maps to NM_148975.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:59943081 C>T maps to NM_152852.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:17998000 C>T maps to NM_001105569.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:47637438 C>T maps to NM_000251.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:47637438 C>T maps to NM_000251.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:47630527 C>T maps to NM_000251.1 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr5:79950716 C>T maps to NM_002439.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr5:79950707 T>C maps to NM_002439.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr5:79950749 T>G maps to NM_002439.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:79950749 T>G maps to NM_002439.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:48027374 T>C maps to NM_000179.2 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38285680 T>C maps to ENST00000398532 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr9:35753721 A>G maps to NM_001044264.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:64955263 G>T did not map to a codon.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr23:64951011 C>T did not map to a codon.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr12:65857047 C>T maps to NM_001031679.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:65857077 C>T maps to NM_001031679.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr4:4864581 G>T maps to NM_002448.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105931108 C>T maps to NM_004689.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:105936203 C>T maps to NM_004689.3 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:121463424 T>C maps to NM_022045.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:242036768 G>A maps to NM_182501.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr14:64921448 G>A maps to NM_005956.3 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:80189276 C>T maps to NM_006441.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:149896206 A>C did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:149896261 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:149899967 A>G did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr15:31266589 A>C maps to NM_017762.2 L134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:9695363 G>C maps to NM_001077525.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:30403306 C>T maps to NM_021090.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:56585592 C>T maps to NM_004687.4 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr13:25831927 C>T maps to NM_004685.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:63568660 C>T did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:63574800 A>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:63488669 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11142528 T>C maps to NM_015458.3 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:187455328 G>A maps to NM_005958.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:11188141 C>T maps to NM_004958.3 T1984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:7892932 A>G maps to NM_024010.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:7893004 C>T maps to NM_024010.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:7892932 A>G maps to NM_024010.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:7893004 C>T maps to NM_024010.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:7873565 C>G maps to NM_024010.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:125575046 G>T maps to NM_014751.4 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:125568484 C>T maps to NM_014751.4 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:17503611 C>G maps to NM_001001924.2 S1212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:17611915 C>T maps to NM_001001924.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr13:30054458 C>T maps to NM_001033602.2 H1129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr13:29675048 A>T maps to NM_001033602.2 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr3:124646709 T>A maps to NM_033049.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:8999043 G>A maps to NM_024690.2 S13600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr19:9033693 G>A maps to NM_024690.2 T12081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr19:9070330 C>T maps to NM_024690.2 A5705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:100678692 T>C maps to NM_001040105.1 Y1332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:100696347 G>T maps to NM_001040105.1 V4395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:100676967 G>A maps to NM_001040105.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:100683795 T>C maps to NM_001040105.1 G3033G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:100677354 A>C maps to NM_001040105.1 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:100678692 T>C maps to NM_001040105.1 Y1332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:1093361 C>G maps to ENST00000441003 T1727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:1103854 C>T maps to ENST00000441003 V2718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:1092842 C>G maps to ENST00000441003 G1554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr6:30955190 G>C maps to NM_001010909.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr6:30954869 T>C maps to NM_001010909.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:30954308 A>T maps to NM_001010909.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:30954326 C>T maps to NM_001010909.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:195505246 G>T maps to NM_018406.5 I4290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr11:1260238 C>A maps to ENST00000447027 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr11:1258273 C>T maps to ENST00000447027 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:1272245 G>A maps to ENST00000447027 T4715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:1258183 C>T maps to ENST00000447027 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:1264940 G>A maps to ENST00000447027 T2280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:1263647 G>A maps to ENST00000447027 V1849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:1281931 C>T maps to ENST00000447027 C5684C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:1272842 C>T maps to ENST00000447027 S4914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:1016629 G>A maps to NM_005961.2 S2057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:105449436 G>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr6:49423827 G>A maps to NM_000255.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:49425445 T>C maps to NM_000255.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr21:42817372 A>G did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:3242041 C>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:3241590 C>T did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:3248332 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:1290407 A>G maps to NM_032348.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:54377235 C>T maps to NM_001020818.1 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4448323 C>T maps to NM_001105538.1 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4458535 T>C maps to NM_001105538.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:4446216 C>T maps to NM_001105538.1 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:4452637 C>T maps to NM_001105538.1 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr8:67492514 A>G maps to NM_001080416.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr8:128750843 C>T maps to NM_002467.4 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr8:128750612 G>A maps to NM_002467.4 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr8:128751020 C>T maps to NM_002467.4 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr8:128752906 A>G maps to NM_002467.4 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr8:128750819 G>A maps to NM_002467.4 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr13:77754318 G>T maps to NM_015057.4 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:10404765 C>T maps to NM_005963.3 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:8416981 C>T maps to ENST00000360416 K873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:8455418 T>C maps to ENST00000360416 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:8413246 G>A maps to ENST00000360416 D991D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr17:8455391 C>T maps to ENST00000360416 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr16:15880585 G>A maps to NM_001040114.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:15841533 G>T maps to NM_001040114.1 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:15931974 G>A maps to NM_001040114.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr17:10267751 G>A maps to NM_003802.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50810404 C>T maps to NM_001145809.1 L1926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:50795616 C>T maps to NM_001145809.1 L1743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:50812314 C>T maps to NM_001145809.1 A1947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:108147509 A>G maps to NM_014981.1 F1197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:108163558 C>T maps to NM_014981.1 Q881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr17:10430003 G>A maps to NM_017534.5 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr14:23852442 G>A maps to NM_002471.3 A1884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:23862709 C>T maps to NM_002471.3 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:33568454 T>C maps to NM_020884.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:33588873 G>A maps to NM_020884.3 T1838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:33586673 C>T maps to NM_020884.3 Y1424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:10312791 C>T maps to NM_002472.2 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:36678815 C>A maps to NM_002473.4 P1927P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:36691690 T>C maps to NM_002473.4 E1115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:36685328 C>T maps to NM_002473.4 E1453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:36708243 G>C maps to NM_002473.4 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:35176540 G>A maps to NM_006097.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:30414620 C>T maps to NM_033118.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:16673799 G>A maps to NM_012334.2 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:16682061 C>T maps to NM_012334.2 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:16701716 C>T maps to NM_012334.2 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:16754990 C>T maps to NM_012334.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:16877738 G>A maps to NM_012334.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr22:26164605 G>A maps to ENST00000407587 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:26168332 C>T maps to ENST00000407587 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:26422992 C>T maps to ENST00000407587 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:26164407 C>G maps to ENST00000407587 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr22:26422650 G>A maps to ENST00000407587 P2239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:26304362 G>A maps to ENST00000407587 E1743E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr22:26242204 C>T maps to ENST00000407587 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:34859830 G>A maps to NM_001163735.1 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:1382888 G>A maps to NM_001080779.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr15:59506885 C>A maps to NM_004998.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:59517010 G>A maps to NM_004998.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:59500969 C>T maps to NM_004998.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:8620635 C>T maps to NM_012335.3 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:109826534 G>A maps to NM_001101421.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:109838953 C>T maps to NM_001101421.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr18:47462674 C>T maps to NM_001080467.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:47462656 G>A maps to NM_001080467.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:47506873 G>T maps to NM_001080467.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:76922207 G>A maps to NM_000260.3 K2021K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:76918410 A>G maps to NM_000260.3 S1940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:128341903 G>A maps to ENST00000389524 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:128367450 C>T maps to ENST00000389524 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr18:3129296 C>T maps to NM_003803.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:2050563 G>A maps to NM_003970.2 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:69934011 C>A maps to NM_032578.2 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:40231809 C>T maps to NM_015460.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:59126850 A>G maps to NM_001085487.1 C773C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:41790865 G>C maps to NM_006766.3 V1624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr2:1796098 C>T maps to ENST00000399161 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:174974264 C>T maps to NM_207015.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:57114434 C>T maps to NM_001113203.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:57118251 C>T maps to NM_001113203.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:59668274 T>A maps to NM_199290.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr9:138903496 G>A maps to NM_144653.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:1688718 C>A maps to ENST00000344463 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:46417624 A>G maps to NM_001029861.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:92928106 C>A did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:92928123 G>T did not map to a codon.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr23:92928070 T>G did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:92927727 T>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:23377814 G>A maps to ENST00000431864 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:60747575 G>A maps to NM_024611.4 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:78279743 T>C maps to NM_024678.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:34133766 G>A maps to NM_024662.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:50334567 G>A maps to NM_012191.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:50334591 G>A maps to NM_012191.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr4:2062887 C>T maps to ENST00000423729 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:20066703 C>T maps to ENST00000396087 A1153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:19735324 C>A maps to ENST00000396087 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:20070348 C>T maps to ENST00000396087 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:19735324 C>A maps to ENST00000396087 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:15679409 G>A maps to NM_015909.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:15607852 G>A maps to NM_015909.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr13:35729912 C>A maps to ENST00000400445 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:203922074 A>G maps to NM_001114132.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:47033969 C>T maps to NM_015175.1 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:47046484 C>T maps to NM_015175.1 Y2106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:21795286 G>A maps to NM_032264.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120378656 G>A maps to NM_001047980.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120378701 A>G maps to NM_001047980.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120386921 A>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:41342736 G>A maps to NM_005899.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:22790830 T>C maps to NM_004540.2 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr21:22656514 G>A maps to NM_004540.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:6634816 C>T maps to NM_014865.3 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:6638196 C>T maps to NM_014865.3 T1188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:183817153 T>C maps to NM_205842.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:183866767 G>A maps to NM_205842.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:133538702 G>A maps to NM_207363.2 G1657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr2:133636474 C>T maps to NM_207363.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:50186584 T>C maps to NM_001037806.3 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:48716536 C>A maps to NM_016453.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:48717275 G>A maps to NM_016453.2 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:232320280 G>A maps to NM_005381.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:3207397 G>A maps to NM_020170.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr20:46279883 A>G maps to NM_181659.2 Q1270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr20:46265034 C>T maps to NM_181659.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:33338098 G>A maps to NM_014071.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:33328371 C>T maps to NM_014071.2 P1896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:15968886 T>C maps to ENST00000395857 Q1636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:16001755 G>A maps to ENST00000395857 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124821704 G>A maps to NM_006312.4 P1910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:124841275 G>A maps to NM_006312.4 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:124886978 C>T maps to NM_006312.4 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:55423581 G>A maps to NM_004829.5 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:41318577 T>C maps to NM_004828.3 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr15:23931596 G>A maps to NM_002487.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140108467 C>T maps to NM_001144026.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr23:43809177 C>T did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:118975188 G>T maps to NM_004784.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:19627082 G>C maps to ENST00000436926 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:60448733 T>C maps to NM_174889.4 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:152486079 G>T maps to NM_001164507.1 A3268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr2:152486100 G>A maps to NM_001164507.1 D3261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr2:152432214 C>A maps to NM_001164507.1 V5669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:152470903 C>T maps to NM_001164507.1 K3829K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:152547267 G>A maps to NM_001164507.1 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:152382758 T>C maps to NM_001164507.1 K7321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:152389990 A>G maps to NM_001164508.1 L7128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:84030847 C>T maps to NM_019065.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:32248087 C>T maps to NM_031232.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr12:8245310 A>G maps to NM_015509.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:29886340 C>T maps to NM_021076.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr22:29884843 C>T maps to NM_021076.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr8:24813639 G>A maps to ENST00000221169 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:24771317 G>A maps to NM_005382.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:75641681 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11640852 C>T maps to NM_145043.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11643730 G>A maps to NM_145043.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:130947465 G>A maps to NM_024800.4 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7221453 G>A maps to NM_032442.2 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7226081 G>A maps to NM_032442.2 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:31378794 G>A maps to NM_022728.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr17:29667602 T>G maps to NM_001042492.2 G2334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:29652883 T>C maps to NM_001042492.2 L1628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:29679400 A>G maps to NM_001042492.2 Q2528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:204939762 C>T maps to ENST00000367172 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:68225196 C>T maps to NM_173165.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:13183881 C>G maps to ENST00000397661 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:103505960 C>T maps to NM_003998.3 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr14:35871694 G>A maps to NM_020529.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:129752425 G>A maps to NM_006165.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:41232587 A>G did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:47579566 G>A did not map to a codon.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr3:25781093 G>A maps to NM_018297.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr10:115636656 A>C maps to NM_198514.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:17750128 G>A did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:71358412 A>G did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:71359554 G>A did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr1:236156993 G>A maps to NM_002508.2 D902D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:52486849 G>A maps to NM_007361.3 C907C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr9:95887258 C>A maps to NM_004148.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:36985750 A>G maps to NM_133433.3 K823K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:36986296 A>G maps to NM_133433.3 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:36985273 C>T maps to NM_133433.3 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:50667298 C>T maps to NM_033119.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:42662975 A>C maps to NM_005385.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:42662975 A>C maps to NM_005385.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:13545609 C>T maps to NM_001189.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:7319123 C>T maps to NM_020795.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:5821467 C>G did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr16:3614076 C>T maps to ENST00000448023 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3613689 G>A maps to ENST00000448023 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:57071166 G>A maps to NM_032206.3 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:54313943 A>C maps to ENST00000391773 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:7064270 T>C maps to NM_176822.3 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:247588139 C>T maps to NM_004895.4 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:56369094 C>T maps to NM_134444.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:56369667 C>T maps to NM_134444.4 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:56369913 C>T maps to NM_134444.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr11:279843 C>T maps to NM_138329.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:284298 A>G maps to NM_138329.1 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:285255 G>A maps to NM_138329.1 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55441970 G>A maps to ENST00000446217 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55451082 A>G maps to ENST00000446217 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:56467166 C>T maps to NM_176811.2 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr19:56244557 G>A maps to NM_176820.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr6:142399928 T>C maps to NM_002511.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr6:142400027 G>T maps to NM_002511.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr16:4516346 G>A maps to NM_020677.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:43181222 C>T maps to NM_021079.3 D437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:232393131 G>A maps to NM_006056.4 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:50746227 G>T maps to NM_022162.1 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:10797951 G>A maps to NM_024894.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:65735053 A>G maps to NM_015462.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:13615766 T>C maps to NM_016167.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:95081568 T>C maps to NM_017948.5 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:95069241 A>G maps to NM_017948.5 N917N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:95076770 A>C maps to NM_017948.5 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:103920254 T>A maps to ENST00000405356 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:103912217 C>A maps to ENST00000405356 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:103919737 G>A maps to ENST00000405356 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:156745223 G>A maps to NM_138400.1 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:2636058 C>T maps to NM_006392.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:203157537 A>G maps to NM_015934.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:203157537 A>G maps to NM_015934.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:117685254 G>A maps to ENST00000338101 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:117691489 G>A maps to ENST00000338101 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:26085930 G>A maps to NM_000625.4 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:26107839 G>A maps to NM_000625.4 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150710391 G>A maps to NM_000603.4 E1060E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139390957 T>C maps to NM_017617.3 P2411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139391635 G>A maps to NM_017617.3 D2185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:139407931 A>G maps to NM_017617.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:139391635 G>A maps to NM_017617.3 D2185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:139399212 G>A maps to NM_017617.3 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:139418259 A>G maps to NM_017617.3 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:139391635 G>A maps to NM_017617.3 D2185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:139407931 A>G maps to NM_017617.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:139413907 C>T maps to NM_017617.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:120458146 G>A maps to NM_024408.2 R2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120480582 G>A maps to NM_024408.2 C1078C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:120458160 G>C maps to NM_024408.2 S2395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:32163540 A>C maps to NM_004557.3 S1895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr17:79912129 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2030028 C>T maps to NM_172168.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:101606809 G>A maps to NM_002518.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:34247746 C>T maps to NM_001164749.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr11:66191693 C>T maps to NM_178864.3 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:108044440 G>A maps to NM_002519.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:53853159 T>C maps to NM_005285.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr20:57269608 G>A maps to NM_024663.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:132441142 C>G maps to ENST00000393156 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:182787796 G>A maps to NM_030769.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:106819088 C>T maps to ENST00000503451 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:35806499 C>T maps to NM_003995.3 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:32712118 T>C maps to ENST00000265074 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:73862605 C>T maps to NM_012428.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:156135249 C>T maps to NM_000910.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr23:30327152 C>T did not map to a codon.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr23:30326888 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38253468 G>A maps to NM_021724.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:119530545 T>C maps to NM_022002.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr12:95442843 C>T maps to NM_003297.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr6:108499426 G>A maps to ENST00000368983 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr4:149002554 G>A maps to ENST00000511528 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:157184994 G>A maps to NM_006186.3 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:127245069 C>T maps to NM_004959.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:127262863 C>T maps to NM_004959.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr1:52306074 T>C maps to NM_002525.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr7:129330334 G>T maps to ENST00000393231 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr5:139260441 G>A maps to NM_013982.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr10:84498368 A>G maps to ENST00000404547 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:16337447 C>A maps to NM_003489.3 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:16337537 G>A maps to NM_003489.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:105168688 C>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:105193708 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:105153117 C>T did not map to a codon.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr2:51254997 C>T maps to ENST00000404971 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:50280468 C>T maps to ENST00000404971 T1396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:50464108 C>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:50779938 G>A maps to ENST00000404971 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:51255306 G>T maps to ENST00000404971 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:152034407 G>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:59508165 A>G maps to NM_001144772.1 N646N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:6622138 G>T maps to NM_017755.5 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:72717685 C>T maps to NM_148956.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:86195097 C>T maps to NM_002526.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:5604063 T>C maps to NM_001102654.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:2094642 G>A maps to NM_002528.5 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:2522535 T>C maps to NM_006181.1 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr12:96076599 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:88576214 G>A maps to NM_001012338.1 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr20:61386044 C>T maps to NM_002531.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:11800179 G>A maps to NM_012344.3 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:205273039 G>A maps to ENST00000441520 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:32319353 G>T maps to NM_025152.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:102895168 C>T maps to NM_031438.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:21965800 C>A maps to NM_024815.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr11:67395799 C>T maps to ENST00000376693 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:88344062 G>C maps to NM_024047.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:45563214 A>G maps to NM_012345.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:27620933 G>A maps to NM_020772.2 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:71725611 A>G maps to ENST00000393695 N985N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:71724783 C>T maps to ENST00000393695 V1261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:71725280 G>A maps to ENST00000393695 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:69090683 A>G maps to NM_020401.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:69090623 C>T maps to NM_020401.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:69113183 C>T maps to NM_020401.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr6:17706505 A>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:37299006 G>A maps to NM_153485.1 G1252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131755890 C>T maps to NM_015354.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:131752486 G>A maps to NM_015354.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:131768785 G>A maps to NM_015354.1 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr3:13427858 G>A maps to NM_024923.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:154115961 A>G maps to NM_207308.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:183993084 A>G maps to NM_138285.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:102494848 T>C maps to NM_024057.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:102494848 T>C maps to NM_024057.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:50412395 C>T maps to NM_012346.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr19:50412089 G>A maps to NM_012346.4 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr19:16860859 C>T maps to ENST00000438489 C469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16860601 T>C maps to ENST00000438489 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:16872793 C>T maps to ENST00000438489 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:102338560 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:120097550 G>A maps to NM_178507.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:113444284 C>T maps to NM_016817.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr1:228522537 G>A maps to NM_001098623.1 P5370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228399627 G>A maps to NM_001098623.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228461654 C>T maps to NM_001098623.1 H1774H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228504485 G>A maps to NM_001098623.1 T4454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228547690 C>T maps to NM_052843.2 P6366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228560180 G>A maps to NM_001098623.1 S7234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228565324 C>T maps to NM_001098623.1 L7805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:228437756 C>A maps to NM_001098623.1 A1375A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6914-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:228401328 C>T maps to NM_001098623.1 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:228476419 C>T maps to NM_001098623.1 P3390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:228495866 G>A maps to NM_001098623.1 E4174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:228557696 C>T maps to NM_001098623.1 N6674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:220422125 G>A maps to NM_015311.2 D1335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:133036742 A>G maps to ENST00000262283 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:133044171 G>A maps to ENST00000262283 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:133053908 G>C maps to ENST00000262283 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:28117059 T>A maps to NM_000275.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr4:48835427 T>A maps to NM_001168254.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:128709153 T>G did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:131245129 G>A maps to NM_153435.1 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:123870853 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:123775823 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:123838881 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:123514899 T>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:123539062 A>C did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:183721087 C>T maps to NM_001080477.1 L2562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr11:78380663 G>A maps to NM_001098816.2 R2242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:78387355 C>T maps to NM_001098816.2 A1779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:13786874 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:50954849 G>A maps to NM_018245.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:50959964 C>T maps to NM_018245.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70777434 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:58999895 C>A maps to NM_145243.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr18:55103349 C>T maps to NM_004852.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:193332565 A>G maps to NM_130837.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:153421998 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr8:54147397 G>A maps to NM_000912.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:62729842 A>G maps to NM_000913.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:6867587 T>C maps to ENST00000379831 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:55735090 C>T maps to NM_001005491.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:22102314 A>G maps to NM_001005466.1 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:22038275 C>T maps to NM_001005465.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:123886647 T>C maps to NM_001004462.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:123886901 A>G maps to NM_001004462.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:123908970 C>T maps to NM_001004463.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16060452 T>C maps to NM_001004465.1 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158435572 C>G maps to NM_001004473.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158436200 T>C maps to NM_001004473.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:158390377 A>T maps to NM_001004476.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr11:57995633 G>T maps to NM_001004471.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158368914 G>T maps to NM_001004475.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:59481213 A>G maps to NM_001005324.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:29365027 G>A maps to NM_013936.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:45799450 C>T maps to NM_001004297.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:107298269 C>A maps to NM_001001961.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:107361037 C>T maps to NM_001004482.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:107361001 C>G maps to NM_001004482.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:107266812 C>T maps to NM_001004485.1 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:247978767 G>A maps to NM_001001966.1 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3301245 G>A maps to NM_003553.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr7:143771335 C>T maps to NM_001004488.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:132021721 G>A maps to NM_030908.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:99474437 A>G maps to NM_001005276.1 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:27879092 G>A maps to NM_033057.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:3406650 G>A maps to NM_012368.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr7:143633275 T>C maps to NM_001004685.1 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr6:29429914 T>C maps to NM_030883.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:29429731 T>C maps to NM_030883.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:29429731 T>C maps to NM_030883.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:29080266 G>A maps to NM_001005216.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:114089882 G>A maps to ENST00000374428 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr1:248202361 C>T maps to NM_001004686.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr1:248224738 A>G maps to NM_001004687.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:248343745 T>C maps to NM_001004688.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr1:248366818 C>T maps to NM_001004689.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr9:35957228 G>T maps to NM_019897.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:248570056 T>C maps to NM_030904.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:248616328 C>T maps to NM_001004136.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:248813351 G>A maps to NM_001001824.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:248813420 G>A maps to NM_001001824.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr1:248059469 C>T maps to NM_001001957.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:3195602 T>A maps to ENST00000397187 K98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:55136156 C>T maps to NM_001005275.1 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr11:55135958 T>C maps to NM_001005275.1 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:51411816 G>A maps to NM_001005272.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:51412065 G>C maps to NM_001005272.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:48347040 T>C maps to NM_001004702.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr11:55433433 C>A maps to NM_001004704.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:59282837 G>A maps to NM_001004711.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:22133691 C>A maps to NM_001001912.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:102346029 G>A maps to NM_001005326.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:20585768 C>T maps to NM_001004715.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr14:20388875 C>A maps to NM_001005483.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:22382648 C>G maps to NM_001005241.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:55419146 C>T maps to NM_001004059.2 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:48285423 A>G maps to NM_001004726.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:5364430 G>A maps to NM_001005567.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:5364475 C>T maps to NM_001005567.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:5364430 G>A maps to NM_001005567.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:5364475 C>T maps to NM_001005567.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr11:5372967 C>A maps to NM_001004750.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:4843118 C>T maps to NM_001004753.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr11:4936071 G>A maps to NM_001005238.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:5020541 A>T maps to NM_001004755.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:4903218 C>T maps to NM_001004759.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:5566459 G>A maps to NM_001005289.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:5566075 G>A maps to NM_001005289.1 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:4608395 A>C maps to NM_001005170.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:6007991 A>G maps to NM_001005173.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:6024030 G>A maps to NM_001005179.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56756564 G>A maps to NM_001005323.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr11:56409696 A>C maps to NM_001002925.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:56431617 C>T maps to NM_001004730.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:55798277 C>T maps to NM_001001921.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:58190227 G>A maps to NM_001005566.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:58275302 G>A maps to NM_001005218.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr11:58170411 G>A maps to NM_001005469.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr9:125551541 C>T maps to NM_001001923.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:55587590 C>T maps to ENST00000395203 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:97852236 A>G maps to NM_001005338.1 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:97852290 A>G maps to NM_001005338.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:55703522 G>A maps to NM_006637.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:55579067 C>T maps to NM_001004738.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr11:55579055 G>A maps to NM_001004738.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:56310328 C>T maps to NM_001005245.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr11:56043713 T>G maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:55999878 C>A maps to NM_001004746.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr11:55681541 C>A maps to NM_001001960.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:55820357 G>A maps to NM_001005183.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:55820684 T>G maps to NM_001005183.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:14952188 G>T maps to NM_001005190.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:14938189 A>G maps to NM_017506.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:124413490 C>T maps to NM_001005195.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:124253041 G>A maps to NM_001005468.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:124135618 T>C maps to ENST00000341493 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56128225 T>C maps to NM_001005205.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:56128030 G>C maps to NM_001005205.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56113702 C>T maps to NM_001002907.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56113922 C>T maps to NM_001002907.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr11:55927378 G>A maps to NM_001004058.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:56143951 T>C maps to NM_001005204.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr11:57958225 C>T maps to NM_001005283.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117094118 G>A maps to NM_000608.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117094199 C>T maps to NM_000608.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:58114676 C>T maps to NM_006812.3 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr3:32022623 G>A maps to NM_017784.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr3:32022419 G>T maps to NM_017784.4 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr3:32022568 G>A maps to NM_017784.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr3:32022572 G>A maps to NM_017784.4 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179226430 A>G maps to ENST00000392505 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:52250215 C>T maps to ENST00000428468 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:83998921 G>A maps to NM_013370.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:190936576 A>G maps to NM_198184.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:38260569 T>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:38262963 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:26699032 G>A maps to NM_194248.2 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:161221261 T>A maps to NM_001080440.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:72926878 T>C maps to NM_178160.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:48783182 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:149916583 C>G maps to NM_020205.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr12:29604410 A>G maps to NM_183378.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:29649190 C>T maps to NM_183378.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:97639020 A>G maps to NM_080818.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:97639826 T>G maps to NM_080818.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:16336380 A>G maps to NM_138381.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr8:107695482 C>T maps to NM_001198533.1 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr17:3599170 G>T maps to ENST00000435558 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:1584573 T>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:1584850 G>C did not map to a codon.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr23:1585399 G>A did not map to a codon.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr23:1585216 G>T did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr23:1585332 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:1584816 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:1585083 A>C did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:1584684 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:1584687 A>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:131539461 T>C maps to NM_001142599.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr8:101721959 C>A did not map to a codon.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr8:101729999 C>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr13:25670626 A>G maps to NM_030979.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:105821456 G>A maps to ENST00000458164 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:17413126 G>A maps to NM_007365.2 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:17410252 G>A maps to NM_007365.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:17668507 C>T maps to NM_012387.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr1:17701956 C>T maps to NM_207421.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:17727846 T>C maps to NM_207421.3 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:55247816 T>C did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:196529916 A>G maps to NM_002577.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:39660291 G>A maps to NM_005884.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:169611764 C>T maps to NM_001166108.1 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:169819834 A>G maps to NM_001166108.1 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr12:56712935 G>C maps to NM_001127460.2 V1104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:28750682 A>G maps to NM_175854.7 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:91359115 C>T maps to NM_148977.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:78915497 C>A maps to NM_173797.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:6753012 C>T maps to NM_006999.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39575986 G>A maps to NM_001004318.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:118950207 G>T maps to NM_002581.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr9:119097143 C>T maps to NM_002581.3 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr1:176671859 G>C maps to NM_020318.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:34630574 T>A maps to NM_019619.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:206110508 T>C maps to ENST00000406610 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:206166287 C>A maps to ENST00000406610 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:49366878 C>T maps to NM_032521.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:183551308 C>T maps to NM_018622.5 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:183580580 C>T maps to NM_018622.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr1:226573324 T>C maps to NM_001618.3 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:3931307 G>A maps to NM_020367.4 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:122419992 C>T maps to NM_017554.2 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:122419209 T>C maps to NM_017554.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:51981768 G>A maps to NM_001003931.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:12540036 T>C maps to NM_018222.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:150840689 G>T did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr22:31741414 C>T maps to NM_014323.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr9:36923481 C>T did not map to a codon.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:18962815 C>T maps to NM_002584.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:113976145 T>C maps to NM_003466.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:27685662 C>T maps to NM_018492.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:19680275 G>A maps to NM_025245.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:134296331 G>A maps to NM_032151.4 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr3:51994889 G>T maps to NM_033010.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:136012636 A>T maps to NM_001178014.1 K252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:91090532 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:91134202 C>A did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:91518116 A>T did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr10:55698631 G>A maps to NM_001142763.1 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr10:55626475 T>G maps to NM_001142763.1 R1220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr10:55663020 A>G maps to NM_001142763.1 T1166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr13:58208449 C>T maps to NM_001040429.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:31144188 C>T maps to NM_001173523.1 R1162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:140167032 T>G maps to NM_018900.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140237093 C>G maps to NM_018901.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140237825 G>C maps to NM_018901.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr5:140249902 G>A maps to NM_018902.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:140251069 C>T maps to NM_018902.3 H794H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140256274 G>A maps to NM_018903.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140256919 G>C maps to NM_018903.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:140256919 G>C maps to NM_018903.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr5:140257189 G>C maps to NM_018903.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr5:140264045 G>A maps to NM_018904.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr5:140263475 C>T maps to NM_018904.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140264090 G>C maps to NM_018904.2 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:140262581 C>G maps to NM_018904.2 Y243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr5:140175766 G>A maps to NM_018905.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr5:140180940 G>A maps to NM_018906.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140188022 C>T maps to NM_018907.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140188391 C>G maps to NM_018907.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:140188352 G>A maps to NM_018907.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:140188355 A>G maps to NM_018907.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140188352 G>A maps to NM_018907.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140188355 A>G maps to NM_018907.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:140188352 G>A maps to NM_018907.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:140188355 A>G maps to NM_018907.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr5:140186915 C>T maps to NM_018907.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr5:140186855 C>T maps to NM_018907.2 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140202820 C>G maps to NM_018908.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140203462 C>A maps to NM_018908.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr5:140209667 G>A maps to NM_018909.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140209592 A>G maps to NM_018909.2 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140216124 G>A maps to NM_018910.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr5:140222522 C>T maps to NM_018911.2 D539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:140222315 G>A maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr5:140229744 G>A maps to NM_031857.1 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140229924 G>C maps to NM_031857.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:140307484 T>C maps to NM_018898.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140346669 C>A maps to NM_018899.5 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:140347901 A>T maps to NM_018899.5 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr5:140346764 A>T maps to NM_018899.5 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr5:140431537 C>T maps to NM_013340.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140573654 C>T maps to NM_018930.3 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140580957 C>A maps to NM_018931.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140589333 A>G maps to NM_018932.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140595830 G>T maps to NM_018933.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140603247 G>A maps to NM_018934.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140603793 C>T maps to NM_018934.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140604693 G>A maps to NM_018934.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:140564227 G>A maps to NM_020957.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140475957 G>T maps to NM_018936.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:140503796 C>T maps to NM_018938.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140503277 T>C maps to NM_018938.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr5:140517067 G>A maps to NM_015669.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:140554428 G>A maps to NM_018940.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:140559057 G>A maps to NM_019120.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:140559147 C>T maps to NM_019120.2 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr5:140711924 C>T maps to NM_018912.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140719293 G>A maps to NM_018915.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:140735360 C>T maps to NM_018917.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr5:140741033 C>T maps to NM_018923.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:140856348 A>G maps to NM_002588.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:120383247 A>G maps to NM_001029996.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:82785095 G>A maps to NM_033026.5 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr8:17843568 T>C maps to NM_006197.3 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:17847417 A>G maps to NM_006197.3 Q1487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:52733126 G>A maps to NM_052937.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr21:47847546 C>T maps to NM_006031.5 T2444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr21:47856915 C>T maps to NM_006031.5 S3007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr21:47831620 C>T maps to NM_006031.5 D1878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr21:47841932 T>C maps to NM_006031.5 P2358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr21:47847699 C>T maps to NM_006031.5 I2495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:71500216 C>T maps to NM_014982.2 Y1210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:71443815 T>G maps to NM_014982.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:65403665 C>T maps to NM_032223.2 A1827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr20:17240883 G>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:1487980 C>T maps to NM_017573.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:1487058 G>T maps to NM_017573.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:78506180 C>A maps to NM_001190482.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:78638796 C>T maps to NM_001190482.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:78789899 A>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:117079686 G>A maps to NM_004716.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:117097930 C>T maps to NM_004716.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:55505650 C>T maps to NM_174936.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:70485331 G>A maps to NM_016297.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:70503953 G>T maps to NM_016297.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:24608244 C>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:98997954 G>A maps to NM_014891.6 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr10:105184916 C>G maps to NM_014976.1 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:170892758 T>A maps to NM_002598.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:112654237 C>T maps to NM_014456.4 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr2:101188049 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:178592451 C>A maps to NM_016953.3 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr12:20787927 A>T maps to NM_000921.3 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:10531490 C>T maps to NM_001111307.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr5:58334736 C>T maps to NM_001104631.1 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:144873982 T>C maps to NM_014644.4 P1658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:144859816 G>A maps to NM_014644.4 S2089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:144859878 G>A maps to NM_014644.4 R2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:149323780 G>A maps to NM_000440.2 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:149324152 G>A maps to NM_000440.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:149265874 G>A maps to NM_000440.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:660339 G>A maps to NM_000283.3 K763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:663877 A>G maps to NM_000283.3 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:85610348 C>T maps to NM_002605.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr22:39627797 G>A maps to NM_002608.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:55130077 T>C maps to NM_006206.4 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:55143576 G>A maps to ENST00000507166 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:55152039 C>T maps to ENST00000507166 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:149511635 C>G maps to NM_002609.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:19369481 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:34969149 C>T maps to NM_003477.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:10929937 G>A maps to ENST00000381611 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:48174793 C>T maps to NM_002611.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr4:95496939 G>A maps to NM_006457.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:95575791 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr8:94935820 C>T maps to NM_001161778.1 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:32093078 A>G maps to NM_178140.2 G2598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:102783353 C>G maps to NM_001195263.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr3:73433730 G>A maps to NM_015009.1 Y662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:41966770 G>A maps to NM_001164595.1 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:22570903 C>T maps to NM_144962.2 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:4119491 T>C maps to NM_206836.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:56763742 G>T maps to NM_021255.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4576622 G>A maps to ENST00000301396 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4586219 G>A maps to ENST00000301396 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:4576194 C>T maps to ENST00000301396 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:57354379 T>C maps to NM_001135690.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:7880584 A>T maps to ENST00000377532 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:138428378 G>A maps to NM_022121.4 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:92118653 G>A maps to NM_000466.2 H1240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr7:92146904 T>C maps to NM_000466.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:10684421 C>A maps to NM_004565.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:45932457 G>A maps to NM_057174.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:160253412 G>A maps to NM_002857.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr3:179525540 G>A maps to NM_016559.1 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr3:179537726 C>T maps to NM_016559.1 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:3177943 C>T maps to NM_002627.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:3178000 G>A maps to NM_002627.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr17:4851556 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:99190184 G>A maps to NM_002629.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:44104804 C>T maps to NM_000290.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:44104912 G>A maps to NM_000290.3 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:44104895 C>T maps to NM_000290.3 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:77225098 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:197711869 G>A maps to NM_024989.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:28251889 C>T maps to NM_032507.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:41710110 G>A maps to NM_002630.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:41704715 G>T maps to NM_002630.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15587066 T>A maps to NM_052890.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:15587102 C>T maps to NM_052890.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:15587102 C>T maps to NM_052890.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr1:64104388 G>A maps to NM_002633.2 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr15:99511838 C>T maps to NM_001102612.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:100933406 G>A maps to NM_000926.4 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:125944130 G>C maps to NM_032177.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:33820519 G>A maps to ENST00000419414 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:169846936 A>G maps to NM_024947.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:22117215 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:170105724 T>C maps to NM_018288.3 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:133901933 C>T maps to ENST00000448712 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:129792786 A>G maps to NM_199320.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:123632172 G>A maps to NM_015651.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:96407952 G>A maps to NM_005392.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:96411413 G>A maps to NM_005392.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:45987090 A>T maps to ENST00000257821 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:64394120 A>G maps to NM_015153.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr6:79671507 C>T maps to NM_017934.5 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:79700647 C>T maps to NM_017934.5 R752R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr23:71855061 G>A did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:47533769 C>T maps to NM_000293.2 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:30762885 C>T maps to NM_000294.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:71683435 A>T maps to NM_015020.2 L1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:139744523 C>T maps to NM_014172.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr11:608545 G>A maps to ENST00000264555 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:582055 G>A maps to ENST00000264555 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:61005203 C>T maps to NM_032439.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:21064269 C>T maps to NM_058004.2 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:4012970 C>T maps to NM_015897.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:4037722 G>A maps to NM_015897.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:65112115 C>T maps to ENST00000333425 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:509849 T>C maps to NM_001127178.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr17:26881922 C>T maps to NM_033198.3 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:44048223 T>C maps to NM_015937.4 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr10:98369475 G>A maps to NM_152309.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:98369562 T>C maps to NM_152309.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:17118729 A>G maps to NM_002645.2 G1400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:204433626 C>T maps to NM_002646.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr12:18491370 T>C maps to NM_004570.4 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:18715672 A>G maps to NM_004570.4 K1168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:39576681 G>A maps to ENST00000398870 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:8733109 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:209190069 T>C maps to NM_015040.3 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:209168941 C>T maps to NM_015040.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:37138371 C>T maps to ENST00000373507 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:37138576 G>A maps to ENST00000373507 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:37138764 C>T maps to ENST00000373507 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:37138950 C>T maps to ENST00000373507 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr6:37138422 G>A maps to ENST00000373507 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr6:37138936 C>T maps to ENST00000373507 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr6:37138423 C>T maps to ENST00000373507 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:37139202 G>A maps to ENST00000373507 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr6:37138419 C>T maps to ENST00000373507 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr6:37138624 C>G maps to ENST00000373507 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr6:37139037 G>T maps to ENST00000373507 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr6:37139190 C>T maps to ENST00000373507 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:37138591 G>A maps to ENST00000373507 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:37138950 C>T maps to ENST00000373507 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:37139103 C>T maps to ENST00000373507 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:37139127 G>A maps to ENST00000373507 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:37138570 G>A maps to ENST00000373507 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:37139091 C>T maps to ENST00000373507 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:37138952 C>A maps to ENST00000373507 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:37138401 C>T maps to ENST00000373507 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr6:37138371 C>T maps to ENST00000373507 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:48775917 G>A did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr23:48775890 C>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:20975046 T>C maps to NM_032409.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:20975643 C>T maps to NM_032409.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:77010660 T>C maps to NM_017439.3 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:22830841 C>T maps to NM_005028.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:36936845 C>T maps to NM_003559.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr22:32015666 G>A maps to ENST00000422296 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:67267635 G>A maps to NM_004910.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr17:6367557 G>C maps to NM_031220.3 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr17:6358849 G>A maps to NM_031220.3 H911H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:94320299 C>T maps to NM_152431.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:68382421 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2152849 A>G maps to NM_001009944.2 A2971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:2161348 G>A maps to NM_001009944.2 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:47924232 G>A maps to NM_138295.3 D1076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:47925608 G>A maps to NM_138295.3 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:47955166 A>G maps to NM_138295.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:81242183 T>C maps to NM_052892.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:46656561 A>G maps to NM_006071.1 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr22:46657893 C>T maps to NM_006071.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:51613011 C>T maps to NM_138694.3 K3134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:51892976 A>G maps to NM_138694.3 N1179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:51771043 G>A maps to NM_138694.3 F2259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:51523889 A>G maps to NM_138694.3 I3678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:110408346 C>T maps to ENST00000426474 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:110413805 G>A maps to ENST00000426474 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:110491800 T>C maps to ENST00000426474 F3037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:72501071 C>T maps to ENST00000419739 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3026955 T>C maps to NM_004203.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131467781 C>T maps to NM_013355.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:201252907 G>A maps to NM_000299.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:159517925 C>T maps to NM_003628.3 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:68289738 C>T maps to NM_012320.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:48558158 G>A maps to NM_003706.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr19:48609796 G>A maps to NM_001159322.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:42363432 T>A maps to NM_178034.3 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:42438379 G>A maps to ENST00000397272 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:160901402 C>T maps to NM_007366.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:133700485 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:145464129 T>C maps to NM_001029869.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:28772952 T>G did not map to a codon.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr20:8130944 C>A maps to NM_015192.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr20:9374296 C>T maps to NM_001172646.1 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr10:95791435 C>T maps to ENST00000371380 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:39802373 C>T maps to NM_002660.2 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:81960782 G>A maps to NM_002661.2 Q838Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:2436255 G>A maps to NM_014638.2 G1285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:17053612 C>T maps to NM_001144382.1 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:200938 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:41382535 C>T maps to NM_001005473.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr12:18841113 T>C maps to ENST00000266505 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr17:4718854 C>T maps to NM_002663.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:40882587 C>T maps to NM_012268.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr8:144993566 G>T maps to NM_201380.2 I3611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:144991427 G>A maps to NM_201380.2 D4324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:145006865 G>A maps to NM_201380.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:145007408 G>A maps to NM_201380.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr8:144997817 C>T maps to NM_201380.2 A2230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:17035909 C>T maps to ENST00000448080 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:73371841 C>G maps to NM_021200.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:30165156 G>T maps to ENST00000436066 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39908214 G>A maps to NM_022835.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:39909393 C>T maps to NM_022835.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:162928 G>C maps to NM_052909.3 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:43552941 G>A maps to NM_014798.2 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:43552811 A>G maps to NM_014798.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr1:16051839 T>C maps to ENST00000420314 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:16054582 C>T maps to ENST00000420314 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:906121 C>T maps to ENST00000379409 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:161159618 T>C maps to NM_000301.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:4511943 A>G maps to NM_001080400.1 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:4513548 G>A maps to NM_001080400.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr5:57755717 G>A maps to NM_006622.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr4:128804640 A>G maps to NM_014264.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:128808619 A>T maps to NM_014264.4 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr3:145841963 T>G maps to NM_182943.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:49029757 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:114863592 T>A did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr10:20432281 A>T maps to NM_032812.7 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr10:20436807 C>T maps to NM_032812.7 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr3:126747902 C>T maps to NM_032242.3 N1579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:126741040 C>T maps to NM_032242.3 R1384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:208227813 C>T maps to NM_025179.3 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:208216537 C>T maps to NM_025179.3 E1295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:153689642 G>A did not map to a codon.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr7:132174143 C>T maps to NM_020911.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:131864656 G>A maps to NM_020911.1 Y1221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:132193224 G>A maps to NM_020911.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr22:50727960 G>A maps to NM_012401.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr22:50714347 G>A maps to NM_012401.2 L1794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:50728062 G>A maps to NM_012401.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50716067 C>T maps to NM_012401.2 A1716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50718940 C>T maps to NM_012401.2 K1384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50720429 G>C maps to NM_012401.2 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr23:153039488 C>T did not map to a codon.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr23:153039096 C>A did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:153037065 C>T did not map to a codon.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr23:153035888 A>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:153043895 G>A did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr12:94543628 C>T maps to NM_005761.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:94631495 C>T maps to NM_005761.1 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr20:56227141 T>C maps to NM_020182.3 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr1:156182901 T>C maps to NM_007221.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr16:72198812 C>T maps to NM_031293.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:6018230 T>C maps to NM_000535.5 E757E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:219206737 C>A maps to NM_015488.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:118231316 C>T maps to NM_001011709.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr10:118220523 C>A maps to NM_001011709.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:152226188 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:46973314 G>A maps to NM_018215.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:46973692 C>T maps to NM_018215.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:46974076 C>T maps to NM_018215.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:37826248 A>G maps to NM_002686.3 K152K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:68385239 C>G maps to NM_020143.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:36269674 T>A maps to ENST00000457797 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr22:44287688 G>A maps to ENST00000216177 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr19:7620540 C>T maps to NM_001166111.1 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:46023294 C>G maps to NM_018129.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:53544270 G>C maps to NM_153703.4 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:127387387 C>T maps to NM_015720.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr23:84586011 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:84600947 T>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:84563193 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:84586064 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:30822454 C>T maps to NM_015352.1 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:46685549 C>T maps to NM_133635.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr21:46707777 T>C maps to NM_133635.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr1:166818481 G>A maps to NM_017542.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:25014015 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:74347243 C>T maps to NM_006591.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr12:133240613 G>A maps to ENST00000455752 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:133233811 G>A maps to ENST00000455752 P1167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:89862236 C>T maps to NM_002693.2 T1066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:121251923 C>T maps to ENST00000393672 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:37501751 T>C maps to NM_022490.1 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7412348 G>A maps to NM_000937.4 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:22107706 C>T maps to NM_001722.2 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:22107985 A>G maps to NM_001722.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:617803 G>A maps to NM_005035.3 H1156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:621147 C>T maps to NM_005035.3 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:75050957 G>A maps to ENST00000257665 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:53103369 C>T maps to NM_182595.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:134393833 A>G maps to NM_007171.3 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr7:95025644 C>T maps to NM_000940.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:121019008 G>C maps to NM_015918.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:105607585 C>T maps to NM_022361.4 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:124464036 T>G maps to NM_015450.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr18:14542890 G>A maps to ENST00000444806 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:132021907 G>A maps to NM_001083538.1 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:16287537 G>A maps to NM_001136213.1 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr19:42603966 G>A maps to ENST00000342301 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr19:42600042 G>A maps to ENST00000342301 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr2:105473227 G>A maps to NM_006236.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:82764219 T>C did not map to a codon.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr4:147560456 T>C maps to NM_004575.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:147561803 C>T maps to NM_004575.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:145719367 G>A maps to NM_002700.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:128428720 C>T maps to NM_001159542.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:149212613 G>T maps to NM_133263.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:149212589 C>T maps to NM_133263.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:42925500 A>G maps to NM_024664.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:18824535 T>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:76797738 G>A maps to NM_006239.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:27829368 T>C maps to NM_003622.3 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:27842051 G>A maps to NM_003622.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr15:64455113 G>A maps to NM_000942.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170493783 T>C maps to NM_004792.2 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr5:102465356 C>T maps to ENST00000451606 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:4935256 G>A maps to NM_002705.4 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:30570373 G>A maps to NM_002714.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55607446 G>A maps to NM_017607.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49377119 C>T maps to NM_014330.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:37791893 A>G maps to ENST00000394271 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr7:113518865 G>A maps to NM_002711.3 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:58514311 C>A maps to NM_006242.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:49142986 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:242122129 A>G maps to NM_002712.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:111637052 T>C maps to NM_181699.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr5:145979851 A>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:322293 G>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:101984389 T>C maps to NM_000944.4 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:94722814 G>A maps to NM_058237.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr19:46878958 C>T maps to NM_006247.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:12918902 G>A maps to NM_023014.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:11508467 G>T maps to NM_005039.3 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:156756947 C>T maps to NM_005973.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:106553288 C>G maps to NM_001198.3 Y418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr11:129801146 G>A maps to NM_020228.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr21:43230668 C>T maps to NM_022115.3 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:3322138 C>T maps to NM_022114.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:3102851 G>A maps to NM_022114.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:108140190 C>T maps to NM_012406.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:81124298 C>T maps to NM_001099403.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr5:23526429 C>T maps to NM_020227.2 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr5:23526711 T>C maps to NM_020227.2 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:23527272 T>C maps to NM_020227.2 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:27354305 C>T maps to NM_013388.4 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:44571007 A>T maps to NM_001171603.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:47295905 C>T maps to NM_020820.3 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr20:47262399 G>A maps to NM_020820.3 R1167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:69104700 G>A maps to NM_024870.2 S1515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:72360196 T>C maps to NM_005041.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:72360223 C>T maps to NM_005041.4 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:62194237 C>T maps to NM_001037335.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:62194237 C>T maps to NM_001037335.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr20:62195767 C>T maps to NM_001037335.2 P1469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:42862430 G>A maps to NM_153026.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr3:64148735 G>A maps to NM_198859.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:40765279 A>G maps to NM_206907.3 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:14204526 G>C maps to NM_002730.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:151257664 A>G maps to NM_016203.3 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:720273 A>G maps to NM_002735.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:106791446 G>A maps to NM_002736.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:24046860 T>C maps to NM_002738.6 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr14:61857974 G>T maps to NM_006255.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:2105426 C>T maps to NM_002744.4 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr14:30046445 A>T maps to NM_002742.2 *913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr14:30046590 A>G maps to NM_002742.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:30066796 G>A maps to NM_002742.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr14:30046637 G>T maps to NM_002742.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:37518104 A>G maps to NM_005813.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:37505107 C>T maps to NM_005813.3 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:53822343 T>C maps to NM_001098512.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr4:82092908 A>G maps to NM_006259.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr21:48069614 C>T maps to NM_206962.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:68390696 C>T maps to NM_019023.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:128186155 G>A maps to ENST00000409048 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36302896 G>A maps to NM_021232.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr2:68882187 G>A maps to NM_138964.2 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:177421274 C>T maps to NM_006261.4 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:13639489 C>T maps to NM_003675.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr19:54632433 C>A maps to NM_015629.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:116041315 T>C maps to NM_004697.3 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:116053894 C>T maps to NM_004697.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr12:50026834 C>T maps to NM_001031698.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:4044108 G>A maps to NM_003913.4 Q571Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:240981361 T>C maps to NM_001080835.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:138724564 G>A maps to NM_001134659.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr3:138762874 C>T maps to NM_001134657.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr6:27219671 G>A maps to NM_005865.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:33799102 G>A maps to NM_007343.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:84233324 G>A maps to NM_153362.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31151926 G>A maps to NM_173502.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228003842 C>T maps to NM_183062.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228003878 C>T maps to NM_183062.2 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:46784531 C>T maps to ENST00000331814 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:31095998 G>A maps to NM_001039503.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:55965665 A>G maps to NM_173814.4 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:79322710 G>A maps to NM_015225.2 D1493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:40909694 T>G maps to NM_181882.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr14:73640276 C>T maps to NM_000021.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43585285 G>A maps to ENST00000449000 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:43575981 C>T maps to NM_031246.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43411149 G>A maps to NM_002782.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43420289 A>G maps to NM_002782.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:43269685 C>T maps to NM_182707.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:87060792 T>A maps to ENST00000276616 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:32809946 G>A maps to NM_148919.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:40478361 T>C maps to NM_006503.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:184023917 A>G maps to NM_002808.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:74334015 C>T maps to NM_002811.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:40985662 G>A maps to NM_176863.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr2:54135500 G>A maps to NM_014614.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:54176358 A>G maps to NM_014614.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:1106142 G>A maps to NM_006814.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:109824360 A>C maps to ENST00000409138 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:97235289 A>G maps to ENST00000370197 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:71618068 A>G maps to NM_024754.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:86352924 A>G maps to NM_017952.5 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:86352924 A>G maps to NM_017952.5 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:98244241 T>C maps to NM_000264.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:98244241 T>C maps to NM_000264.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:45292925 C>G maps to NM_003738.4 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:11561576 C>T maps to NM_020780.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr10:27703149 C>T maps to NM_001034842.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:132510959 G>A maps to NM_004878.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:117484580 C>T maps to NM_020440.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:117527443 C>T maps to NM_020440.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:47124578 C>T maps to NM_000960.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:48156248 G>A maps to NM_000961.3 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:46939455 G>C did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr2:209358137 A>C maps to NM_005048.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:141840573 G>A maps to NM_005607.4 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr7:136936057 G>A maps to NM_002825.5 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50361873 A>G maps to NM_017432.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:64289967 G>T maps to NM_003463.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:64289995 C>T maps to NM_003463.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:49191190 A>G maps to NM_002827.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:49197954 C>T maps to NM_002827.2 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:49195748 G>A maps to NM_002827.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:87653593 A>G maps to NM_080685.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:87696622 C>T maps to NM_080685.2 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:47453658 G>T maps to NM_015466.2 P1383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:112145798 G>A maps to NM_002829.3 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:112145816 C>T maps to NM_002829.3 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:120734588 T>A maps to NM_002830.2 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr12:7061260 C>T maps to ENST00000416215 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:75762325 G>T maps to NM_002833.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:2969014 C>G maps to NM_002836.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr20:3007336 T>G maps to NM_002836.3 L540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr1:44085858 C>T maps to NM_002840.3 I1735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:44019304 C>T maps to NM_002840.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:61975386 G>A maps to NM_002841.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr3:62189307 C>T maps to NM_002841.3 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:48166641 C>T maps to NM_002843.3 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:48157624 C>T maps to NM_002843.3 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:157959869 G>T maps to NM_002847.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:157959887 G>A maps to NM_002847.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:15699554 G>C maps to NM_030667.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:15677868 T>C maps to NM_030667.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:71286605 G>A maps to NM_002849.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:41408885 G>A maps to ENST00000373198 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr7:121650462 A>C maps to NM_002851.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:121652963 T>C maps to NM_002851.2 S1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:40556950 C>T maps to NM_012232.5 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1536113 C>A maps to NM_001013658.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1536116 G>A maps to NM_001013658.1 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1536137 T>C maps to NM_001013658.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1536356 G>A maps to NM_001013658.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:1537509 C>T maps to NM_001013658.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:31441315 T>C maps to ENST00000373741 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:20508155 C>T maps to ENST00000361078 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:44130204 G>A maps to NM_031292.3 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45150762 G>A maps to NM_006505.3 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45368804 C>T maps to NM_001042724.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:45381648 C>T maps to NM_002856.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:134218801 G>T maps to NM_138499.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:134219290 C>T maps to NM_138499.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr2:1680760 G>A maps to NM_012293.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:1647185 G>A maps to NM_012293.1 D1302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:1653226 G>A maps to NM_012293.1 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:52321237 G>A maps to NM_144651.4 A982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:58376937 G>A maps to NM_017771.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:133272589 G>T maps to NM_018663.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr14:51378472 G>A maps to NM_002863.4 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:64520568 G>A maps to NM_005609.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:133768826 G>A maps to NM_198180.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:136467083 G>A maps to ENST00000409606 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:8468321 A>G maps to NM_004218.3 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:37732508 G>A maps to NM_001002814.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr8:37732262 T>C maps to NM_001002814.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:570736 G>A maps to NM_014700.3 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:73339674 C>T maps to NM_015470.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140125877 C>T maps to ENST00000275874 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:66043585 G>A maps to NM_030981.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr20:56929268 A>G maps to NM_020673.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:11436220 A>G maps to NM_004283.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:11436220 A>G maps to NM_004283.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr1:220326664 G>A maps to ENST00000358951 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr11:61675609 G>A maps to NM_013401.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr23:102755450 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102192371 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102192884 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:229431612 T>C maps to NM_004578.2 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:56383857 C>T maps to NM_002868.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:13727322 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:125748668 A>G maps to NM_012197.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:50384468 A>G maps to NM_013277.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:68710031 G>A maps to NM_133339.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:68292186 T>C maps to NM_133509.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:95423463 A>G maps to NM_012415.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:4876063 G>A maps to NM_018059.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:4876099 G>A maps to NM_018059.4 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr17:17701757 C>T maps to ENST00000395776 T1832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:17696525 G>A maps to ENST00000395776 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:17698022 C>T maps to ENST00000395776 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:20565511 T>A maps to NM_020343.3 K843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:37199442 G>A maps to NM_020336.2 E1365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:37203570 A>G maps to NM_020336.2 S1482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr9:135982492 C>T maps to NM_006266.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr12:131359241 G>A maps to ENST00000392369 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:20112867 C>T maps to NM_002882.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:6012346 T>A maps to NM_012416.2 V1087V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:21932597 G>A maps to NM_001145658.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:2911351 C>T maps to NM_015085.4 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:134503414 C>T maps to NM_198679.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr2:173882185 C>T maps to NM_007023.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr2:204304224 G>T maps to ENST00000374493 R1282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr2:204304542 G>A maps to ENST00000374493 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr2:204305401 C>T maps to ENST00000374493 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr3:25611288 G>A maps to NM_000965.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:88279281 T>C maps to NM_020320.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:86681124 A>T maps to NM_002890.1 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:65357557 A>G maps to NM_016563.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr15:65347440 G>A maps to NM_016563.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:4768281 G>A maps to NM_014737.2 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:45488737 G>A maps to NM_032023.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr12:86198770 G>A maps to NM_005447.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr19:10428228 C>T maps to NM_133452.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:10439500 C>T maps to NM_133452.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:10439539 A>G maps to NM_133452.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:65243465 A>G maps to ENST00000294428 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:3771683 G>A maps to NM_032753.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:48947552 C>T maps to NM_000321.2 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:49039404 T>A maps to NM_000321.2 L797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:33134864 A>C maps to NM_005610.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr23:16881136 A>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47041413 C>T did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:47045744 G>A did not map to a codon.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr11:66391988 C>A maps to NM_006328.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:110884492 T>C maps to NM_022768.4 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:155114111 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:114358448 C>T maps to NM_016196.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:114386722 G>A maps to NM_016196.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr5:145631421 T>C maps to NM_018989.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36124821 C>A maps to NM_024321.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:50147060 G>A maps to NM_005778.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr3:29938966 G>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:135961559 C>G did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr23:129545347 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:89449167 T>A maps to NM_019610.5 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr11:7111163 G>A maps to NM_014469.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:48388507 G>C maps to NM_002900.2 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr1:173916597 G>A maps to NM_172071.2 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:103173755 C>A maps to NM_015156.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:10124256 C>T maps to NM_015725.2 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:110118458 T>C maps to ENST00000405097 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:145740621 C>T maps to ENST00000428558 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr17:73654376 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:73624465 G>A maps to NM_004259.5 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:73657117 C>T maps to NM_004259.5 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1495326 C>T maps to ENST00000395479 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:65422373 C>T maps to NM_021975.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:103205948 G>C maps to ENST00000428762 T1662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150068980 G>A maps to NM_001099695.1 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr6:139262507 A>G maps to ENST00000367663 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:8420965 G>A maps to NM_012102.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:43615093 C>T maps to NM_020975.4 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:43615632 C>G maps to NM_020975.4 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:85577908 C>A maps to NM_017750.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:85570439 G>A maps to NM_017750.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:111695303 A>G maps to NM_002912.3 N1418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:111631253 T>C maps to NM_002912.3 R2948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr6:111685067 T>C maps to NM_002912.3 K2289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:111656670 C>T did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:1827926 T>G maps to NM_020695.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:39306503 C>G maps to ENST00000381897 R681R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:32756806 G>C maps to NM_001098535.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:32754285 G>A maps to NM_001098535.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr3:16419278 G>A maps to NM_015150.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:198460747 T>G maps to NM_144629.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:74664697 A>G maps to NM_018124.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:74664697 A>G maps to NM_018124.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr19:14076564 C>G maps to NM_002918.4 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:107114547 G>A maps to ENST00000357881 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr6:117248413 C>T maps to NM_173560.3 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr15:56387863 G>A maps to NM_022841.5 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:56387420 T>C maps to NM_022841.5 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:56387580 C>T maps to NM_022841.5 W782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:109697657 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:109696757 T>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:71350293 A>G did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr19:11529919 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:93588656 G>A maps to NM_020211.2 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:113127772 A>G maps to NM_005054.2 P1760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr5:176795189 C>T maps to ENST00000398128 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr9:116346319 G>T maps to NM_144488.4 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr14:72943454 G>A maps to NM_004296.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:240975228 C>T maps to ENST00000407727 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:182640847 G>A maps to NM_033345.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:182638778 C>T maps to NM_001102450.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:227860231 C>T maps to NM_001167608.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr22:29660103 C>T maps to NM_012265.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:30615882 C>T maps to NM_138328.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr1:156347191 G>A maps to NM_020407.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr2:20647759 G>A maps to NM_004040.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr8:144462840 G>A maps to ENST00000422773 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:38950760 A>G maps to ENST00000296782 D1063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:38960005 G>A maps to ENST00000296782 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr2:152300224 T>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:152320500 T>C maps to NM_018151.4 T1489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:8926014 C>T maps to NM_020734.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr8:104513173 G>A maps to NM_001100117.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:104513155 C>A maps to NM_001100117.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr20:43385537 C>A did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:43386413 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:66099887 C>T maps to NM_004292.2 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr20:19915768 C>T maps to ENST00000255006 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:19955712 G>C maps to ENST00000255006 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:19937288 C>T maps to ENST00000255006 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:19955472 C>T maps to ENST00000255006 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:105182994 G>A maps to NM_021930.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:3083368 T>C maps to NM_003804.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:90770392 C>T maps to NM_003821.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr21:43161042 G>A maps to ENST00000352483 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:89753545 G>C maps to NM_000326.4 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:5335589 T>G maps to NM_006911.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr14:21360198 G>A maps to NM_002935.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:19319352 C>T maps to NM_007148.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr3:49751412 C>T maps to NM_022064.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr23:105970553 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:179393866 T>C maps to NM_018434.4 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:122338663 T>C maps to NM_139175.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:18457573 C>T maps to NM_182757.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:158596031 G>A maps to NM_144726.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:74208465 A>G maps to NM_052916.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr18:44015314 A>G maps to NM_152470.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:25374635 A>G maps to ENST00000381927 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr5:63626165 C>T maps to NM_001113561.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:6267522 C>T maps to NM_207396.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78263633 A>G maps to NM_020914.4 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:78338304 C>T maps to NM_020914.4 V3990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr11:117109652 T>C maps to NM_207343.2 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr7:5662541 C>T maps to NM_207111.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:5765033 C>T maps to NM_207111.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:125397810 C>T maps to NM_152553.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:30780860 C>T maps to NM_014771.2 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:56601997 G>A maps to NM_194359.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr17:58034593 G>A maps to NM_016125.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:89554107 T>A maps to NM_003800.3 K413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:89614520 G>A maps to NM_003800.3 D199D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FF-8041-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr17:685704 G>A maps to NM_018146.2 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:78667094 C>T maps to NM_002941.3 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:78676700 T>C maps to NM_002941.3 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:79174618 C>T maps to NM_002941.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr3:77147264 G>A maps to ENST00000332191 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr11:124748632 C>T maps to NM_022370.3 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:124764175 T>C maps to NM_019055.5 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:124764175 T>C maps to NM_019055.5 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:11484211 C>A maps to NM_004850.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr5:10465049 A>C maps to NM_031916.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:64643649 C>T maps to NM_005012.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:94499796 A>G maps to NM_004560.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:94499796 A>G maps to NM_004560.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr15:61521303 C>T maps to NM_134261.2 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:117681559 G>T maps to NM_002944.2 A1130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:55533804 G>T maps to NM_006269.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr8:10470002 C>T maps to NM_178857.5 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:10464464 G>A maps to NM_178857.5 L2381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:10464473 G>T maps to NM_178857.5 L2378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr8:10469291 C>T maps to NM_178857.5 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:10469291 C>T maps to NM_178857.5 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:48075596 A>G maps to NM_024604.2 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:68904644 C>A maps to NM_000329.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:68914352 A>G maps to NM_000329.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:38145714 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:38145840 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:38145917 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:53639447 G>A maps to NM_015272.2 V1260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr14:47120687 G>C maps to NM_080746.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:101619210 C>T maps to NM_000993.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:12877703 G>A maps to ENST00000273223 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr3:197678056 C>T maps to NM_000996.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:40834594 G>A maps to NM_000997.4 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:93299192 G>A maps to NM_000969.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr8:74204060 G>C maps to ENST00000396470 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:120636497 G>A maps to NM_053275.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:1440373 C>T maps to NM_001018.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:79814746 C>T maps to NM_001142285.1 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:79814611 T>C maps to NM_001142285.1 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr23:83357091 C>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:78936338 G>A maps to NM_020761.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:9885227 G>T maps to NM_173659.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr11:126075444 C>T maps to NM_032795.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:39325135 C>T maps to NM_022157.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr11:14300970 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:7246993 C>T maps to NM_001003699.3 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:7230224 C>T maps to NM_001003699.3 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:15166808 A>G maps to NM_018427.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:99126512 C>T maps to NM_015179.3 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:99130281 T>G maps to NM_015179.3 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:99150236 G>A maps to NM_015179.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:99126512 C>T maps to NM_015179.3 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr10:99150236 G>A maps to NM_015179.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:48561870 G>A maps to NM_018346.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr21:43913111 G>A maps to NM_080860.2 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:46313917 C>G maps to NM_030785.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr6:127476584 T>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:101350273 C>T maps to NM_001134888.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:63487032 T>C maps to ENST00000377819 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr17:1840011 C>T maps to NM_178568.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:1840731 G>A maps to NM_178568.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:187419763 G>A maps to NM_001004312.2 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:70143825 T>C maps to NM_017987.4 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:33937214 C>T maps to NM_016568.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:33162506 G>A maps to ENST00000374685 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr1:237580415 A>C maps to NM_001035.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:237620033 G>A maps to NM_001035.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:237947170 G>A maps to NM_001035.2 E4053E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:34030766 G>T maps to NM_001036.3 G2544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:34105083 A>G maps to NM_001036.3 K3426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:34111968 C>T maps to NM_001036.3 D3573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:33842399 A>T maps to NM_001036.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:33842399 A>T maps to NM_001036.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:33954551 T>C maps to NM_001036.3 Y1607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:34130696 G>C maps to NM_001036.3 V4172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:34137130 G>A maps to NM_001036.3 E4455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:153520202 G>A maps to NM_002960.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr1:153507186 T>C maps to NM_014624.3 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:6698663 G>A maps to NM_005980.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:33292188 C>T maps to NM_022753.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:101704771 C>A maps to NM_001400.4 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr19:10335122 C>T maps to NM_004230.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:10624862 C>T maps to NM_001166215.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr13:23907901 A>C maps to NM_014363.4 T3371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr13:23908804 A>G maps to NM_014363.4 V3070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:23905480 C>T maps to NM_014363.4 P4178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:23914285 T>C maps to NM_014363.4 E1243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr13:23908090 G>A maps to NM_014363.4 H3308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:47700541 T>C maps to NM_005500.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:5590290 G>T maps to NM_014649.2 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:51173822 G>A maps to ENST00000251020 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr18:76757144 C>T maps to NM_171999.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:50406645 A>G maps to NM_020436.3 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:50406891 C>T maps to NM_020436.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:50408613 A>G maps to NM_020436.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr20:50407254 G>A maps to NM_020436.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:39873857 T>G maps to NM_018028.2 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:92734357 G>A maps to NM_017654.3 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50874850 G>A maps to ENST00000216061 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:68341660 C>A maps to NM_001164160.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:133945287 C>T maps to NM_016103.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr9:136577805 C>T maps to NM_007101.3 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:136577769 C>T maps to NM_007101.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:136595252 C>T maps to NM_007101.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr17:26708752 C>T maps to ENST00000379061 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39410464 G>A maps to NM_017827.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:39416934 C>T maps to NM_017827.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50899102 G>A maps to ENST00000337034 D1012D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr22:50885657 C>T maps to ENST00000337034 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:50893667 C>G maps to ENST00000337034 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr11:10051374 G>A maps to NM_030962.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:1109576 C>T maps to NM_014963.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:36018271 C>T maps to NM_001166034.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50157979 G>A maps to NM_021228.2 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:75305057 G>T maps to ENST00000361900 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:77025686 C>T maps to ENST00000324767 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:27516322 G>A maps to NM_016240.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:224462713 G>A maps to NM_003469.4 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr4:129864288 T>C maps to NM_144643.2 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:108029132 C>T maps to NM_198081.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:38739415 C>T maps to NM_006514.2 S1765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr3:38924722 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:166868774 A>G maps to NM_001165963.1 Y1241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:166900424 C>T maps to NM_001165963.1 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr2:166201312 C>T maps to NM_001040142.1 R937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:123516315 G>A maps to NM_018400.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:62018736 G>A maps to NM_000334.4 I1635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:62029005 A>G maps to NM_000334.4 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr12:52200498 C>A maps to NM_014191.2 I1743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:167145105 C>A maps to ENST00000303354 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:167128971 G>A maps to ENST00000303354 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:6472752 C>A maps to NM_001159576.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr12:6471386 G>A maps to NM_001159576.1 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:10595249 T>C maps to NM_004589.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:144895017 C>T maps to NM_182706.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:45917702 C>T maps to NM_138355.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:45917702 C>T maps to NM_138355.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:65293818 G>A maps to NM_020680.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:65293818 G>A maps to NM_020680.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:65293818 G>A maps to NM_020680.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:31349794 G>A maps to NM_014654.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:31349641 C>T maps to NM_014654.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr1:243437858 T>C maps to NM_006642.3 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:26982340 A>G maps to NM_006923.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:256507 C>T maps to NM_004168.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:256507 C>T maps to NM_004168.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr1:161326590 C>T maps to NM_003001.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr7:4153850 C>T maps to NM_152744.3 N1256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:3991478 A>G maps to NM_152744.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:4116696 G>A maps to NM_152744.3 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr17:71434181 G>A maps to NM_001144952.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:82033021 A>G maps to NM_145168.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:85234857 T>C maps to NM_014300.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr22:30867894 G>C maps to NM_174975.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:5050677 C>T maps to NM_014692.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:5061190 C>T maps to NM_014692.1 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr9:139371029 A>C maps to NM_014866.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139370828 G>A maps to NM_014866.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr20:18492907 C>T maps to NM_001172745.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:110384429 T>C maps to NM_006323.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr10:75526106 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:119659517 G>A maps to ENST00000379735 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:102262226 C>G maps to NM_015490.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:12200091 A>G maps to NM_018144.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr7:54823512 G>A maps to NM_014302.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:169700524 C>G maps to NM_003262.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:81969157 A>G maps to NM_005065.4 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:169697217 G>A maps to NM_000450.2 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:169677561 G>A maps to NM_000655.4 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr7:83610790 G>A maps to NM_006080.2 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:83764112 T>C maps to NM_006080.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:80380644 G>T maps to NM_006379.2 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr7:84685038 A>G maps to NM_152754.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:83035288 A>G maps to NM_012431.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr7:83036445 G>A maps to NM_012431.2 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:52476245 G>A maps to NM_020163.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr1:156146493 G>A maps to NM_022367.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr2:97531444 G>A maps to NM_017789.4 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr5:9119195 G>A maps to NM_003966.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr3:122632727 G>A maps to NM_001031702.2 C703C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:115827505 G>A maps to ENST00000257414 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:4558421 C>A maps to NM_032108.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:4555078 G>A maps to NM_032108.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr15:48063876 G>A maps to NM_153618.1 R1039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:43851100 T>C maps to NM_003008.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:7474728 C>T maps to ENST00000321337 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:76373001 G>A maps to NM_015571.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr17:56599356 G>A maps to NM_004574.3 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr22:19709200 G>T maps to NM_002688.5 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:118797637 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:75471761 G>A maps to NM_001113495.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:67895778 G>A maps to NM_001018067.1 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:94844974 G>A maps to NM_001127707.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:95058476 G>A maps to NM_000624.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:61234090 C>T maps to ENST00000382768 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:61565013 C>T maps to NM_001143818.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr18:61471520 G>A maps to NM_001040147.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:61471592 A>G maps to NM_001040147.1 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr6:2890534 T>C maps to NM_004155.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:21134022 G>A maps to NM_000185.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:51936078 T>C maps to NM_001101320.1 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:57373645 C>T maps to ENST00000403558 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:167170787 G>A maps to NM_006217.3 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179986552 T>C maps to NM_178123.4 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:42530294 G>A maps to NM_015559.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:30978323 C>A maps to NM_014712.1 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:9483817 C>G maps to ENST00000407969 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:123892234 G>A maps to NM_020382.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr12:123892234 G>A maps to NM_020382.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:26688400 T>C maps to NM_021115.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:2248184 A>T maps to NM_007165.4 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:38433761 G>A maps to NM_006802.2 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:198270016 T>C maps to NM_012433.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:198257074 G>A maps to NM_012433.2 N1289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:24291322 G>A maps to NM_016047.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:149895865 G>A maps to NM_005850.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr10:7412242 G>A maps to NM_001018039.1 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr17:56083866 A>C maps to NM_006924.4 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:56083704 A>G maps to NM_006924.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:64020240 T>C maps to ENST00000513458 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45561013 A>G maps to NM_007056.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:45563694 G>A maps to NM_007056.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:1718202 C>G did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr23:1712438 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:99848997 A>C maps to NM_032870.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:46321416 G>A maps to NM_004719.2 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:46339032 A>G maps to NM_004719.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132237788 C>T maps to NM_004592.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:132239987 G>A maps to NM_004592.2 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:85893841 C>T maps to NM_198843.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr10:81702260 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:104486488 C>T maps to NM_178858.4 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:104486821 C>T maps to NM_178858.4 P80P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FF-8043-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:156184785 G>A maps to NM_172244.2 *257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr7:94218022 C>T maps to NM_001099401.1 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:23853546 C>T maps to NM_000231.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:67148008 G>A maps to ENST00000237247 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr6:134494229 C>A maps to NM_001143676.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:134493824 G>A maps to NM_001143676.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:134495710 C>T maps to NM_001143676.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:134495154 G>A maps to NM_001143676.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:134495217 G>A maps to NM_001143676.1 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:42977590 G>C maps to NM_032237.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:8175867 C>T maps to NM_001080826.1 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:8176050 G>A maps to NM_001080826.1 Y1278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:8176539 C>T maps to NM_001080826.1 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:108816879 G>A maps to NM_152621.5 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr10:72633214 C>T maps to NM_003901.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr17:78184538 G>A maps to NM_000199.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:25251026 T>C maps to NM_001039948.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:25264352 C>T maps to NM_001039948.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr10:82329985 T>C maps to NM_207372.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:38051492 G>T maps to NM_018957.3 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:38044340 C>T maps to NM_018957.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:2828968 G>A maps to NM_001145856.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:235951182 G>A maps to NM_014521.2 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr4:152069109 A>C maps to NM_001009555.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:87170605 G>A maps to ENST00000482504 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr10:105362349 G>A maps to ENST00000369774 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr4:170043267 C>T maps to NM_020870.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr4:8224645 C>T maps to NM_018986.3 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:8229377 C>A maps to NM_018986.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr11:70505971 C>T maps to ENST00000338508 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:51160580 C>T maps to NM_001080420.1 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:154938075 G>A maps to NM_001130040.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:91652976 G>A maps to NM_016848.5 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:146267375 T>C maps to ENST00000367503 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:132159798 G>A maps to NM_001172700.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:9863928 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:77476808 T>C maps to NM_020859.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:77660549 T>C maps to NM_020859.3 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:164750324 A>G maps to NM_001041.3 Y907Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:150480588 G>A maps to NM_005067.5 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:113285271 A>C maps to ENST00000393830 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:117063019 C>T maps to NM_001040455.1 H641H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:3670645 C>T maps to NM_023068.3 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:3672745 G>A maps to NM_023068.3 A1378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:3674169 G>A maps to NM_023068.3 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:51919230 A>G maps to NM_033130.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr18:43422148 G>A maps to NM_213602.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:52131126 C>T maps to ENST00000222107 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:51650519 C>T maps to NM_014385.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:51961518 C>A maps to NM_014442.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:111594519 G>A maps to NM_015191.1 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:16973723 G>A maps to NM_015260.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:39587219 C>A maps to NM_003616.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:72090808 G>A maps to NM_015556.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:232575050 G>A maps to NM_020808.3 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:1546905 C>T maps to NM_006065.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr17:79872226 C>T maps to NM_016538.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:31928038 C>G maps to NM_006929.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:54674962 T>C maps to NM_015360.4 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr5:54635972 T>G maps to NM_015360.4 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:56928554 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:56904074 C>T maps to NM_000339.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:124829056 A>G maps to NM_001195483.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:100456505 C>T maps to NM_020246.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:100464052 G>A maps to NM_020246.2 E857E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:100463491 G>A maps to NM_020246.2 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr17:6607293 G>A maps to NM_177550.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:111543326 G>A maps to NM_018593.4 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr10:91195993 G>A maps to NM_213606.3 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr17:6941795 C>T maps to NM_201566.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:73096198 C>T maps to ENST00000450736 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:66267733 T>C maps to NM_004694.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr22:38478665 C>G did not map to a codon.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr11:22364887 C>T maps to NM_020346.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:49937048 C>T maps to NM_020309.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr10:119003545 G>A maps to NM_003054.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr21:46935612 G>A maps to NM_194255.1 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:169446638 C>A maps to NM_006996.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:228566992 G>A maps to NM_025243.3 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:47280586 G>A maps to NM_005628.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:15083554 G>A maps to NM_005071.1 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:64337279 G>A maps to NM_018484.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:3284096 C>T maps to ENST00000436008 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:62931546 T>C did not map to a codon.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr5:131630329 G>A maps to NM_003059.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:4855308 G>A maps to NM_203327.1 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:4855308 G>A maps to NM_203327.1 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr2:220033468 C>T maps to NM_001144890.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:220034376 C>A maps to NM_001144890.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:95820499 C>T maps to NM_001160210.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:95864215 G>A maps to NM_001160210.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:794789 G>A maps to NM_001191061.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:87476291 A>G maps to NM_018843.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:87483584 T>A maps to NM_018843.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:19217080 C>A maps to NM_178526.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:1510876 G>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:58017664 G>A maps to NM_133489.2 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:78201685 C>T maps to NM_173626.3 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr7:107330630 C>A maps to NM_000441.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr8:92330560 T>C maps to NM_134266.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:35987424 T>C maps to NM_052961.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr15:50475034 C>T maps to NM_003645.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:85448795 A>T maps to NM_004213.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:85478572 C>A maps to NM_004213.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:45556162 T>C maps to NM_004212.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr10:73122283 G>A maps to NM_018344.5 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:5339048 C>T maps to NM_153247.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:7985317 C>A maps to NM_153449.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:130162229 C>G maps to NM_014580.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr4:9998475 A>G maps to NM_020041.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:27481660 G>A maps to NM_003459.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:45778827 G>A maps to NM_013309.4 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:45814310 A>T maps to NM_013309.4 L81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr15:45814492 C>T maps to NM_013309.4 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:140127724 C>T maps to NM_080877.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:112292764 C>T maps to NM_017945.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:44223291 C>T maps to NM_178148.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:1663959 G>A maps to NM_182838.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr12:69140523 C>T maps to NM_018656.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:31032880 G>A maps to NM_001001479.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:31032880 G>A maps to NM_001001479.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:140048444 G>A maps to NM_207113.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:46622958 T>C maps to NM_030674.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:48326269 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:84050217 G>A maps to NM_001080442.1 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:62648747 C>T maps to NM_001012661.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:190437571 G>A maps to NM_014585.5 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:1494659 G>A maps to ENST00000382147 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:1479962 G>A maps to ENST00000382147 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:10748563 G>A maps to NM_020428.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:10713211 G>A maps to NM_001145056.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:95330439 C>T maps to NM_001114106.1 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:142228385 C>T maps to NM_001080431.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:26731958 G>C maps to ENST00000440501 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:19607431 C>T maps to NM_152908.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:19607431 C>T maps to NM_152908.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:3209253 G>A maps to NM_001174090.1 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:27886819 G>T maps to NM_018158.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:27886843 G>A maps to NM_018158.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150768848 C>T maps to NM_003040.3 C755C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:72338466 C>T maps to NM_001098484.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:51855008 T>G maps to NM_001039960.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:51856158 C>T maps to NM_001039960.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:51856158 C>T maps to NM_001039960.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:26700343 G>C maps to NM_178498.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:32647801 C>T maps to NM_014227.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:17988793 C>T maps to NM_000453.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:17999238 C>T maps to NM_000453.2 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr12:101603482 G>A maps to NM_145913.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr3:11064090 G>A maps to NM_003042.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr3:10976836 G>A maps to NM_014229.1 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:115588849 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr23:115584182 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49793619 C>T maps to NM_014037.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr19:49812602 G>A maps to NM_014037.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr5:1406386 G>A maps to NM_001044.4 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:1409225 G>C maps to NM_001044.4 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:20652290 C>T maps to NM_004211.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr3:170198933 G>A maps to NM_020949.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:33333178 C>T maps to NM_014270.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr2:40655833 T>C maps to NM_021097.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:40656755 A>T maps to NM_021097.2 L222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:70512963 G>A maps to NM_183002.1 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173516914 G>A maps to NM_178527.3 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173552702 G>A maps to NM_178527.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr5:480028 C>T maps to NM_004174.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:491905 G>A maps to NM_004174.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:103148867 G>A maps to NM_001011552.3 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:67300057 G>A maps to NM_004594.2 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:46618167 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:48472097 A>G maps to ENST00000417961 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:48503305 G>A maps to ENST00000417961 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:143185919 A>G maps to NM_173653.3 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:21377716 C>G maps to NM_006446.4 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:133653565 G>A maps to NM_005630.2 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:101815887 T>C maps to NM_173488.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:33586110 G>A maps to NM_144975.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr4:20619094 G>A maps to ENST00000273739 A1403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:20533612 C>G maps to ENST00000273739 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr13:84455213 T>C maps to NM_052910.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr13:84454424 C>A maps to NM_052910.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:144904786 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:144906369 A>G did not map to a codon.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr23:144905285 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:142717382 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:142718180 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:57743530 A>G maps to ENST00000428312 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:143822611 G>A maps to NM_020427.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:128582380 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:2029195 G>A maps to NM_003070.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr4:144467949 A>C maps to NM_003601.2 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr12:56559414 C>T maps to NM_003075.3 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:53407995 G>A did not map to a codon.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr22:45802438 T>G maps to NM_148674.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:45750919 A>G maps to NM_148674.3 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:106888977 C>T maps to NM_001042550.1 Y836Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:106901505 A>G maps to NM_001042550.1 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:2667004 T>C maps to NM_015295.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:2740797 A>T maps to NM_015295.2 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:2203461 T>C maps to NM_017575.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr7:128846327 G>C maps to NM_005631.4 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:128843276 C>T maps to NM_005631.4 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:6413107 T>C maps to NM_000543.4 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr11:6412879 C>T maps to NM_000543.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr6:109764546 C>T maps to NM_003080.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr6:123116915 T>C maps to NM_006714.3 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:57317521 A>G maps to ENST00000457912 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:33071878 T>C maps to NM_018225.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr7:98652486 G>C maps to NM_020429.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:62567986 G>A maps to NM_022739.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:88396212 G>A maps to NM_198274.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:88387507 C>A maps to NM_198274.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr2:88402590 G>T maps to NM_198274.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:10258374 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:84303272 G>A maps to NM_014841.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:15453155 C>T maps to NM_001039697.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:139276447 A>G maps to NM_003086.2 H715H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:43345042 C>T maps to NM_017719.4 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:123950407 A>G maps to NM_180699.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:101835305 G>C maps to NM_003090.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:69318148 T>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:78205188 T>C maps to NM_012245.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr7:17874489 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:50709791 C>T maps to NM_182854.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr20:44469594 C>T maps to NM_033421.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:151638485 T>C maps to ENST00000458013 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:151630818 C>T maps to ENST00000458013 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:17923042 G>A maps to NM_152227.1 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:17949049 A>G maps to NM_152227.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr7:2304006 G>A maps to NM_013321.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr16:11348971 C>A maps to NM_003745.1 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr16:11349095 G>A maps to NM_003745.1 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr16:11348807 C>T maps to NM_003745.1 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:11348806 G>A maps to NM_003745.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:11348987 G>A maps to NM_003745.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr17:76354834 C>A maps to NM_003955.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr9:138590932 C>T maps to NM_001101677.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:602429 C>T maps to NM_005632.2 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:97154761 G>A maps to NM_001034954.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:186573816 C>T maps to ENST00000355634 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:186536234 G>A maps to ENST00000355634 H1006H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr10:108389122 G>A maps to NM_001013031.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr10:106959774 C>T maps to NM_014978.1 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr11:121429297 A>G did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr14:50626656 C>T maps to NM_006939.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:38379542 G>A maps to NM_006941.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:306732 G>A maps to NM_006943.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr17:7492685 C>T maps to NM_006942.1 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:231327183 C>T maps to NM_001080391.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:21468933 C>T maps to NM_003112.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:20825270 C>T maps to NM_182700.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr11:124564251 A>G maps to NM_017425.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:31323885 C>T maps to NM_173847.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34204167 G>A maps to NM_003116.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34205079 C>T maps to NM_003116.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:34208868 G>A maps to NM_003116.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:26919343 T>C maps to NM_006461.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:26911203 C>T maps to NM_006461.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:4863573 G>A maps to NM_004890.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35811214 C>T maps to NM_001039592.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35811748 C>T maps to NM_001039592.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:144337285 G>A did not map to a codon.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr23:142795337 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:217824487 T>C maps to NM_138796.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:16748431 C>T maps to NM_198546.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:16748431 C>T maps to NM_198546.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:45695611 C>T maps to NM_024063.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr5:94994491 C>T maps to NM_031952.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:201284178 G>C maps to ENST00000409151 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:34507304 C>T maps to NM_012391.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr6:34511926 C>T maps to NM_012391.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:44046899 G>A maps to NM_175064.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7324587 G>A maps to NM_199339.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr1:16235855 C>T maps to NM_015001.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr1:16255387 G>T maps to NM_015001.2 E885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:16256986 C>T maps to NM_015001.2 R1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49131316 G>T maps to NM_020126.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:49132645 G>A maps to NM_020126.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:228882587 T>C maps to NM_001142644.1 K994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:57021349 C>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:147207604 G>A maps to NM_003122.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:147553828 C>T maps to NM_001001325.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:44174305 G>A maps to ENST00000396669 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:28995210 C>T maps to NM_032038.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:28995210 C>T maps to NM_032038.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:4434030 G>A maps to NM_001124758.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr20:55910491 G>A maps to ENST00000371258 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:136448207 A>G maps to NM_004598.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73826774 G>A maps to NM_014767.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:51023215 G>C maps to NM_032802.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:51017487 G>T maps to NM_032802.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:38882746 G>A maps to NM_001042522.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr13:80911240 G>T maps to NM_005842.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:155004001 C>A did not map to a codon.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr5:141694496 G>A maps to NM_030964.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:158618319 G>A maps to NM_003126.2 D1231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:158592780 G>A maps to NM_003126.2 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:158614069 G>A maps to NM_003126.2 D1437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr1:158622385 A>T maps to NM_003126.2 Y1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131362360 T>C maps to NM_001130438.2 D1182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131395567 C>T maps to NM_001130438.2 T2463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:54895681 C>T maps to NM_003128.2 F2357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr11:66472274 C>T maps to NM_006946.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:66476402 G>A maps to NM_006946.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:41066401 G>A maps to NM_025213.2 *679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:42162466 G>A maps to ENST00000320955 R1883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:79617038 A>G maps to NM_032567.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:179260660 G>A maps to NM_003900.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:179263541 C>T maps to NM_003900.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:142747229 G>A maps to NM_001080415.1 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:142747226 G>A maps to NM_001080415.1 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr16:30747921 C>T maps to NM_006662.2 R2329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:43146104 G>T maps to NM_003131.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:4245655 G>A maps to ENST00000330063 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:74060167 T>C maps to NM_014230.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:38033414 T>C did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr1:24996751 A>T maps to NM_005839.3 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr16:2819195 G>C maps to NM_016333.3 S2644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18542200 C>T maps to NM_032627.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:109198831 G>A maps to NM_018984.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149485986 T>A maps to NM_198455.2 C1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149486725 T>C maps to NM_198455.2 V1501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149488908 C>T maps to NM_198455.2 D1751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149489442 C>A maps to NM_198455.2 R1867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149493518 C>T maps to NM_198455.2 Q2200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149509047 C>T maps to NM_198455.2 S3201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149512266 C>T maps to NM_198455.2 C3532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:149520552 G>A maps to NM_198455.2 P4461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:149492639 G>A maps to NM_198455.2 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:149485556 C>T maps to NM_198455.2 H1322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:155988107 A>G maps to ENST00000368312 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:57100999 G>C maps to NM_003146.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:57099660 T>C maps to NM_003146.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr20:23016713 C>A maps to NM_001052.2 C198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr20:23016818 C>T maps to NM_001052.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1128900 C>T maps to NM_001053.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:1129440 G>A maps to NM_001053.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:48209472 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:48213498 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:130079573 C>T maps to NM_021978.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:134478177 A>G maps to NM_173344.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:186760532 C>T maps to NM_003032.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr2:107460133 G>T maps to NM_001142351.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:76878096 G>A maps to NM_152996.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:77510007 C>A maps to NM_030965.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:77334231 G>A maps to NM_030965.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:130656799 G>A maps to NM_013443.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr1:113153626 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:113153535 T>C maps to NM_017744.4 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr3:52549476 C>T maps to NM_015136.2 F1301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:104089585 C>T maps to NM_017564.9 I1182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:104025445 G>A maps to NM_017564.9 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:123182891 A>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:123184081 A>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:123176492 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:74077555 G>T maps to NM_213622.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:33704345 C>T maps to NM_178007.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:33741715 C>T maps to NM_178007.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:37815304 G>A maps to NM_006804.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:67938391 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:40498634 C>T maps to NM_139276.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr2:191905871 G>T maps to NM_003151.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:74526080 G>A maps to NM_001164380.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:44076710 G>A maps to NM_001007532.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr19:1220489 C>T maps to NM_000455.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:1207175 C>A maps to NM_000455.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:220474113 C>T maps to NM_052902.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr7:43664437 C>G maps to NM_004760.2 Y414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:23811821 A>G maps to NM_031414.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr4:5333090 G>A maps to NM_018401.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:134038808 G>A maps to NM_173575.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr2:219538410 C>T maps to NM_015690.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:27450670 G>T maps to NM_015000.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:36820014 T>C maps to ENST00000373130 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:124110367 C>T maps to NM_004099.4 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:61787891 C>T maps to NM_001003787.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr9:125923279 A>G maps to NM_018387.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr14:31404489 A>C maps to NM_001083893.1 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:57242601 G>A maps to NM_001001433.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr20:57227076 T>C maps to NM_001001433.1 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:7712049 C>T maps to ENST00000441779 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr3:151599266 C>T maps to NM_033050.4 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr4:70615485 G>A maps to NM_014465.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr17:73177274 G>A maps to NM_006937.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:21841523 A>G maps to NM_007192.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr19:39948336 C>T maps to NM_003169.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr19:39950581 C>A maps to NM_003169.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:27883957 C>T maps to NM_014860.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:70940065 C>T maps to NM_003171.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr22:24583606 C>T maps to NM_019601.3 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:48558887 C>T did not map to a codon.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr15:91835704 C>T maps to NM_014848.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:113169815 T>C maps to ENST00000374463 G2691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:113170322 G>A maps to ENST00000374463 T2522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:113233737 T>C maps to ENST00000374463 A968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:113265447 A>G maps to ENST00000374463 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:115537342 T>C maps to NM_003176.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:58441611 C>T maps to NM_014258.2 T1386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:10964014 G>A maps to NM_001040274.2 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr19:46352061 G>A maps to NM_004819.2 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:46320217 G>A maps to NM_004819.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr6:152768598 C>G maps to NM_182961.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:152457794 C>T maps to NM_182961.2 E8539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:152763257 T>C maps to NM_182961.2 T1320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:64461913 A>G maps to NM_182914.2 E978E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:64519052 C>T maps to NM_182914.2 L2808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:64604633 T>C maps to NM_182914.2 L4926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:64688334 G>A maps to NM_182914.2 A6701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:64580060 C>T maps to NM_182914.2 G4204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:33393582 C>T maps to NM_006772.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:33419592 G>A maps to NM_006772.2 P1314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:33391269 T>C maps to NM_006772.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:33409005 G>A maps to NM_006772.2 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:39777879 C>T maps to NM_004711.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:48879374 C>T maps to NM_012451.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:49047923 A>G did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr14:62536399 C>T maps to NM_031914.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:202569554 C>T maps to NM_177402.4 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:85435741 C>T maps to ENST00000359152 K1110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:85435804 T>C maps to ENST00000359152 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:99955924 T>C did not map to a codon.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr23:37965973 G>T did not map to a codon.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:37935843 G>A did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr6:166578141 T>C maps to NM_003181.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:132967031 T>G maps to NM_138327.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:149699332 A>G maps to NM_015093.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr23:30873152 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:38677241 G>A maps to ENST00000379931 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr10:123843061 C>T maps to NM_206862.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:123970512 G>A maps to NM_206862.2 T2191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70586195 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70595131 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:70627476 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:120793331 T>C maps to NM_003184.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:229750088 T>C maps to NM_014409.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:100547803 G>C did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:100547804 C>T did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:100547805 C>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:160074131 G>T maps to NM_033394.2 G1123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:162036194 C>T maps to NM_004180.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr16:29996995 C>T maps to NM_016151.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr4:16168277 C>T maps to NM_153365.2 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:16165116 T>C maps to NM_153365.2 Q506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr4:16165143 T>C maps to NM_153365.2 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:150470181 A>G maps to NM_025150.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr1:19175987 G>A maps to NM_152232.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:19166893 G>A maps to NM_152232.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:19180859 G>A maps to NM_152232.2 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:19175943 C>T maps to NM_152232.2 W453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:1268461 G>A maps to NM_152228.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:11286687 C>T maps to NM_001097643.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:11183034 C>T maps to NM_176885.2 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:71602664 C>T maps to NM_000353.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr3:10318157 C>T maps to NM_014760.3 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:10311948 T>C maps to NM_014760.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:10312632 G>A maps to NM_014760.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr10:96163176 T>C maps to NM_015188.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr4:7008365 T>C maps to NM_001113361.1 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:77984167 G>A maps to NM_019020.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:50386252 C>T maps to NM_024682.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:50381801 T>C maps to NM_024682.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr9:100971023 G>A maps to NM_018421.3 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2546355 T>C maps to ENST00000434757 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:78317678 C>T maps to NM_144572.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:106083303 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:106116882 T>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:179297261 T>C maps to NM_198868.2 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:179297351 A>G maps to NM_198868.2 C876C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:179300130 T>C maps to NM_198868.2 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:42713451 C>T maps to NM_003192.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:2028219 A>G maps to NM_006453.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:119427936 G>A maps to ENST00000369429 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:59480546 C>T maps to NM_005994.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:115118721 G>A maps to NM_016569.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr17:59560606 C>T maps to ENST00000393853 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:59560750 G>A maps to ENST00000393853 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:92264735 A>G maps to NM_001128596.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:23720500 C>T maps to NM_003196.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:102864250 C>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:24077553 T>C maps to NM_003198.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:44559577 G>A maps to NM_016427.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:44561068 G>T maps to NM_016427.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr18:44560336 G>T maps to NM_016427.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:145838646 C>T maps to NM_006706.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:57384060 A>G maps to NM_207036.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr15:57565431 C>T maps to NM_207036.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:1615392 C>T maps to NM_003200.2 E571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr19:1650208 G>A maps to NM_003200.2 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:52901893 A>G maps to ENST00000398339 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:152083805 C>T maps to NM_007113.2 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:149755844 A>G maps to ENST00000451292 E698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr6:160208812 G>A maps to NM_030752.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:44249938 G>A maps to NM_182539.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr12:111066587 C>T maps to NM_001082538.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:124171537 C>G maps to NM_024809.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:124172642 C>T maps to NM_024809.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:90451499 A>G maps to NM_018319.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:24653282 T>C maps to NM_016614.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:24653282 T>C maps to NM_016614.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:49862721 C>T maps to NM_003598.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:3120179 G>A maps to NM_003213.3 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:97852442 C>T maps to ENST00000379795 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr4:65165690 C>A did not map to a codon.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr11:120989138 C>T maps to NM_005422.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr11:121028665 C>T maps to NM_005422.2 N1474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr22:41790178 G>A maps to ENST00000417325 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:15217534 C>T maps to NM_031898.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:95537329 G>A maps to NM_144705.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:95539832 C>T maps to NM_144705.2 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:10769872 G>A maps to NM_144674.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:1253917 C>T maps to NM_198253.2 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr9:35608459 G>A maps to NM_006285.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35608961 C>T maps to NM_006285.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr10:70405863 A>G maps to NM_030625.2 K1126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr4:106155164 T>G maps to ENST00000513237 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr4:106193849 A>T maps to ENST00000513237 K1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:106156982 G>A maps to ENST00000513237 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:74275173 C>T maps to ENST00000409262 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:74320088 C>T maps to ENST00000409262 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:104464673 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:104464359 G>A did not map to a codon.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr23:104464742 C>T did not map to a codon.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr8:30701913 C>T maps to NM_031271.3 E1540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr17:62290116 G>T maps to NM_018469.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:133486987 C>T maps to NM_001063.3 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr6:50791292 C>A maps to ENST00000263046 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:141678666 G>A maps to NM_001178139.1 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:132352229 C>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:132351702 C>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:132352229 C>G did not map to a codon.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr23:132351081 G>A did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:115580892 G>A maps to NM_012252.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr3:100455432 T>G maps to NM_001007565.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:26899694 G>A maps to NM_012143.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr7:100226978 G>A maps to NM_003227.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:100226936 G>A maps to NM_003227.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:195787101 C>T maps to NM_001128148.1 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:133898948 C>T maps to NM_003235.4 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:133899437 C>T maps to NM_003235.4 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:134145884 G>A maps to NM_003235.4 S2723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:133980075 G>A maps to NM_003235.4 E1908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:105924698 G>A maps to NM_004257.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr18:3451988 G>A maps to NM_170695.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:3452261 C>T maps to NM_170695.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr20:35219311 G>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:36766590 G>A maps to NM_004613.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:2377203 C>T maps to NM_198994.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:2377203 C>T maps to NM_198994.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr15:43577070 G>A maps to NM_052955.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:2190981 A>G maps to NM_199292.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:2191005 C>T maps to NM_199292.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:2190981 A>G maps to NM_199292.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:2191005 C>T maps to NM_199292.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr11:2189154 C>T maps to NM_199292.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:43571346 G>A maps to ENST00000330266 D1420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:242572692 C>T maps to NM_015963.5 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr4:76452234 C>T maps to NM_144721.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:23029970 G>T maps to NM_000361.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr20:23028812 G>A maps to NM_000361.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:39874091 C>T maps to NM_003246.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:39880817 C>T maps to NM_003246.2 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr15:39880817 C>T maps to NM_003246.2 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr6:169632987 G>A maps to NM_003247.2 D592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:373530 C>T maps to NM_016585.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:25314004 G>A maps to NM_024838.4 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr18:216548 C>T maps to NM_005131.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:264029 A>G maps to NM_005131.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:264038 C>A maps to NM_005131.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:27401175 G>C maps to NM_004740.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:155458561 C>T maps to ENST00000456144 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr1:43779452 G>T maps to NM_005424.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:56822689 C>T maps to NM_003920.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:24709350 C>T maps to NM_001099274.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:30012208 A>C maps to NM_003257.3 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:71851079 C>T maps to NM_004817.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:3747889 C>T maps to NM_014428.1 Y840Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr23:153537782 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:84302310 A>G maps to NM_005077.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr4:166913968 C>T maps to ENST00000507499 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35714268 G>A maps to NM_006289.3 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:35708424 T>C maps to NM_006289.3 L1461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr15:63128103 G>A maps to NM_015059.2 A2402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:63102152 C>T maps to NM_015059.2 D2231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:63125803 G>A maps to NM_015059.2 Q2368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:38799492 A>G maps to NM_003263.3 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:187004543 C>T maps to NM_003265.2 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:120476364 G>A maps to NM_138554.3 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:223285041 G>A maps to NM_003268.5 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr5:170736473 G>A maps to NM_021025.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr3:196050861 A>G maps to NM_138461.2 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:64882440 G>A maps to NM_003273.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr8:105361802 C>T maps to NM_030788.2 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr13:100204537 G>C maps to NM_004800.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:98282082 C>T maps to NM_020123.3 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:50153059 A>G maps to NM_001098576.1 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr16:19481008 C>T maps to NM_001105248.1 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:19056694 C>T maps to NM_024847.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:76130575 C>T maps to NM_152468.4 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:20073018 C>T maps to NM_181719.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:42092266 C>T maps to NM_032376.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:72784930 C>T maps to NM_017728.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr7:98449155 C>G maps to NM_001134450.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:125900103 A>T maps to NM_052907.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:130184611 C>T maps to NM_133448.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr11:87024483 G>A maps to NM_022918.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:86782565 A>T maps to NM_022918.3 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:10751378 C>T maps to NM_030969.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:66062013 G>A maps to NM_153266.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr7:112415374 T>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:72424268 T>G maps to NM_173490.6 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:150498772 C>T maps to NM_018487.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:26684706 T>A maps to ENST00000457710 L5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:29447764 G>T maps to NM_001003682.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:9671934 C>T maps to NM_001130924.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140099674 G>A maps to NM_053045.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:1584293 C>T maps to NM_024600.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr2:27260570 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:124972113 G>A maps to NM_001080546.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:75965984 G>A maps to NM_018247.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:120194673 C>T maps to NM_183240.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:120194679 C>G maps to NM_183240.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:9305135 G>A maps to NM_015012.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:194325102 G>A maps to NM_001166305.1 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:129722511 C>T maps to NM_138788.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr1:33363888 C>T maps to NM_033504.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:25757606 C>T maps to NM_018202.4 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:55451849 G>A maps to NM_182532.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:226050502 G>A maps to NM_014698.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr6:44117618 C>T maps to NM_018426.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:91637928 T>C maps to NM_001008495.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:91638018 T>C maps to NM_001008495.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:46159156 C>T maps to NM_016486.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr8:74893544 C>T maps to NM_017866.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:45430152 G>A maps to NM_001123376.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:156255559 G>A maps to NM_032323.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35842479 A>G maps to ENST00000360192 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:35845997 G>C maps to ENST00000360192 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:201115963 G>A maps to ENST00000421960 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CX-01A-12D-A382-10 chr20:24565616 C>T maps to NM_024893.1 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr17:3572622 G>A maps to NM_031298.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr12:98931351 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:69094471 A>T maps to NM_182502.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:69098114 A>G maps to NM_182502.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:69100199 A>G maps to NM_182502.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:68934514 A>G maps to NM_207407.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr12:51237781 G>A maps to NM_182559.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr11:117789316 T>C maps to ENST00000413475 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:117789316 T>C maps to ENST00000413475 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr22:37485625 G>A maps to ENST00000381792 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:2389812 C>T maps to NM_182973.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:2421856 C>T maps to NM_182973.1 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr23:12994467 C>A did not map to a codon.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:12994406 G>C did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:12994911 G>C did not map to a codon.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:12994393 C>G did not map to a codon.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr13:101287334 C>A maps to NM_032813.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr13:101266579 G>A maps to NM_032813.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr20:8000140 C>T maps to NM_021156.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:117810650 G>A maps to NM_002160.2 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr6:31543607 C>T maps to NM_000594.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:31543634 G>A maps to NM_000594.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:31544591 G>C did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:103601636 C>T maps to NM_006291.2 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr6:138200147 A>G maps to NM_006290.2 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:138200318 C>A maps to NM_006290.2 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr5:118728685 G>A maps to NM_014350.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:22960654 C>T maps to ENST00000356864 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:23002085 G>A maps to NM_003840.3 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:60027235 C>T maps to NM_003839.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:2493167 G>A maps to NM_003820.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:1140870 G>A maps to NM_004195.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:6524648 T>C maps to ENST00000355862 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:6525256 C>T maps to ENST00000355862 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr20:62328310 G>T maps to ENST00000482936 P1366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:7995151 G>A maps to NM_001561.5 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7460513 G>A maps to NM_003809.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:7287991 C>A maps to NM_003985.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:195594930 C>T maps to NM_001010938.1 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:9584175 T>C maps to NM_003747.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:57070088 C>T maps to NM_033396.2 P1509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:57070169 C>T maps to NM_033396.2 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr11:57080937 C>A maps to NM_033396.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr11:57081003 G>A maps to NM_033396.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:55645538 G>A maps to NM_003283.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr5:72173115 G>A maps to NM_002270.3 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12813682 T>C maps to NM_001136196.1 E753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12816558 G>T maps to NM_001136196.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:175335161 T>C maps to NM_003285.2 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:5352730 G>A maps to NM_001080495.2 T2597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:5410813 G>C maps to NM_001080495.2 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:5417092 G>T maps to NM_001080495.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:24802203 C>T maps to NM_014494.2 D747D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr17:76045907 C>T maps to NM_001142640.1 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr17:38645132 G>A maps to NM_032865.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr6:32020561 G>A maps to ENST00000375244 G3000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32014189 G>A maps to ENST00000375244 T3456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32032688 C>T maps to ENST00000375244 S2250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:32046831 C>T maps to ENST00000375244 P1451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:35713930 C>T maps to ENST00000451197 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr17:53007451 C>A maps to NM_005486.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:144399992 G>A maps to NM_052963.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:38546273 A>C maps to ENST00000357601 T1507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:38564362 G>A maps to ENST00000357601 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:18217957 C>T maps to NM_004618.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr22:22323002 C>A maps to NM_003935.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D4-01A-11D-A31X-10 chr17:7574034 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:223984071 G>A maps to NM_001031685.2 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:95942772 G>A maps to NM_033285.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr12:113733829 C>T maps to NM_001143819.1 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr20:62521255 G>A maps to NM_199360.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:16186864 G>A maps to NM_001145160.1 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr2:1491692 G>A maps to NM_000547.5 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:1418209 G>A maps to NM_000547.5 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:140086939 C>T maps to NM_001128228.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:48305730 G>T maps to NM_198479.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:26937197 C>G maps to NM_003595.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr21:10971305 G>A maps to NM_199261.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:123671612 C>T maps to NM_001190945.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:139814930 G>T maps to ENST00000359662 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr14:103336726 G>A maps to NM_145725.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:118005457 C>T maps to NM_152402.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:36887862 G>A maps to NM_014831.2 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:36898698 G>A maps to NM_014831.2 C794C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45518395 G>A maps to NM_003274.4 S1109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:140743459 G>A maps to NM_031466.5 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:140999001 G>A maps to NM_031466.5 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:141381102 G>A maps to NM_031466.5 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:141461016 G>A maps to NM_031466.5 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:17243609 C>T maps to NM_004412.5 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr6:123869635 A>G maps to NM_006073.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr6:41196732 C>T maps to NM_198153.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:42233528 G>A maps to NM_033502.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:152710184 T>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:152710521 C>A did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr12:73046813 G>A maps to NM_013381.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:100857169 A>G maps to NM_033219.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr9:100862338 C>A maps to NM_033219.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:30131526 G>T maps to NM_033229.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:15532429 G>A maps to ENST00000455584 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:228602458 G>A maps to NM_016102.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:5719648 T>C maps to NM_006074.4 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr11:5730436 G>A maps to NM_006074.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:119996489 G>A maps to NM_012101.3 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:6486913 C>T maps to NM_033278.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:114482846 T>C maps to NM_018700.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr6:25983695 T>A maps to NM_006355.2 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr3:140406660 C>T maps to NM_152616.4 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:72732847 G>T maps to NM_178125.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:27521505 G>A maps to NM_032546.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr8:67067877 G>A maps to NM_033058.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr7:100730706 T>C maps to NM_030961.1 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:26384972 G>A maps to NM_032588.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:231298969 T>C maps to NM_001004342.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31235547 G>C maps to NM_001008274.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:14291258 G>A maps to NM_007118.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr22:38122288 C>T maps to NM_001039141.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:38129310 C>T maps to NM_001039141.2 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:13220733 G>A maps to NM_001136035.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:13218416 T>C maps to NM_001136035.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:126319452 C>T maps to NM_001031712.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr22:20103263 C>T maps to ENST00000439169 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:100278557 T>C did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:5924827 A>G maps to NM_015939.3 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:38211045 T>C maps to NM_003306.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr13:38237563 A>G maps to NM_003306.1 N559N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr13:38211045 T>C maps to NM_003306.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr20:33665968 C>T maps to NM_015638.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr23:111090429 G>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:111020095 C>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr15:31327778 G>A maps to NM_002420.4 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45825817 C>T maps to ENST00000397932 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:45856962 T>C maps to ENST00000397932 D1410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr9:73461393 G>A maps to ENST00000419692 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9U4-01A-11D-A38X-10 chr9:73225578 G>T maps to ENST00000419692 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr9:73477847 T>A maps to ENST00000419692 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:2428433 G>A maps to ENST00000452833 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:116631901 C>A maps to NM_014112.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:142573331 C>T maps to NM_018646.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:142573612 C>T maps to NM_018646.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr7:142574543 G>A maps to NM_018646.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:98558921 G>A maps to ENST00000359863 T2169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:98592334 G>A maps to ENST00000359863 T3377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:141955389 C>T maps to NM_001001317.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:135771681 C>T maps to NM_000368.4 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr9:135804238 G>A maps to NM_000368.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr16:2136841 C>T maps to NM_000548.3 S1653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr1:184020963 C>A maps to NM_052965.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:73000130 G>A maps to NM_005786.4 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr19:31768073 G>A maps to NM_020856.2 D875D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:31767716 G>A maps to NM_020856.2 H994H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:31768490 G>A maps to NM_020856.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:31768889 G>A maps to NM_020856.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:231665037 C>T maps to NM_005999.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:82269157 C>T maps to NM_030927.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:44948262 C>T maps to ENST00000425677 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:3389558 C>T maps to ENST00000407263 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr23:53112145 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:112770053 G>A maps to NM_032028.3 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:19626086 C>T maps to NM_032037.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:37414320 G>A maps to NM_003312.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TX-01A-11D-A382-10 chr6:43250766 G>A maps to NM_032538.1 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:113234602 G>A maps to NM_017868.3 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:3392020 C>T maps to NM_016030.5 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr3:39174703 C>A maps to ENST00000301819 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:166771841 A>G maps to NM_024753.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:38524225 A>G maps to NM_003316.3 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:38572564 C>T maps to NM_003316.3 H1961H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr21:38520898 T>C maps to NM_003316.3 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:15191208 A>G maps to NM_152574.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:15189790 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:55197319 G>A maps to NM_004623.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:47249047 G>A maps to ENST00000394850 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:89343669 G>C maps to NM_144596.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr14:89319358 G>A maps to NM_144596.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr14:71109097 G>A maps to NM_015351.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:117637965 A>G maps to NM_003594.3 Q1004Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:43447890 C>T maps to NM_012263.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:124633017 C>T maps to NM_001139442.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr6:167754359 C>T maps to NM_031949.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr3:9874913 C>T maps to NM_001025930.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:9874913 C>T maps to NM_001025930.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr14:76232468 C>T maps to NM_015072.4 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr17:46877016 C>T maps to NM_001130918.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr2:179593296 G>A maps to NM_133378.4 S5208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr2:179600637 G>A maps to NM_133378.4 D3601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179577869 T>C maps to NM_133378.4 T7753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179586778 A>G maps to NM_133378.4 H6293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179594589 T>A maps to NM_133378.4 T4886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179598398 C>T maps to NM_133378.4 T3995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179610476 A>G maps to ENST00000375038 D5552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179611679 G>A maps to ENST00000375038 Y5151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179613257 A>C maps to ENST00000375038 S4625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:179614058 T>C maps to ENST00000375038 Q4358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr2:179613650 G>A maps to ENST00000375038 D4494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr2:179606589 T>C maps to NM_133437.3 Q3619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:179396572 T>G maps to NM_133378.4 T32355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179611808 A>G maps to ENST00000375038 Y5108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179611846 T>G maps to ENST00000375038 R5096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179611850 C>T maps to ENST00000375038 L5094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179611874 A>G maps to ENST00000375038 Y5086Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:179611883 T>C maps to ENST00000375038 L5083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:6495198 C>T maps to NM_006087.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:94561 G>A maps to NM_177987.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:135106717 G>A maps to NM_006659.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:135106549 G>A maps to NM_006659.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50667858 A>G maps to NM_020461.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr22:50660063 C>T maps to NM_020461.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr11:62343666 A>T maps to NM_022830.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr7:19738328 T>C maps to NM_001002926.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:48096100 A>G maps to NM_003328.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr22:36872872 C>T maps to NM_012473.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:11773260 G>C maps to ENST00000356957 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:11785485 G>A maps to ENST00000356957 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:7883385 G>A maps to NM_030810.3 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:10472451 G>A maps to NM_003331.4 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr15:41862435 A>G did not map to a codon.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr15:41862355 T>C did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:36398453 G>C maps to NM_003332.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:36398453 G>C maps to NM_003332.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:12702304 T>A maps to NM_000550.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr21:44513241 C>T maps to NM_001025203.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:56181018 C>T maps to NM_007279.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:56181018 C>T maps to NM_007279.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr15:70960859 T>C maps to NM_018003.2 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:70957105 A>G maps to NM_018003.2 N1336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:70959575 C>T maps to NM_018003.2 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:70960421 C>T maps to NM_018003.2 E867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:70968849 A>G maps to NM_018003.2 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:162560208 G>A maps to ENST00000367925 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:162549370 G>A maps to ENST00000367925 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47070260 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47070467 A>C did not map to a codon.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:118715489 G>T did not map to a codon.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr23:118708867 C>T did not map to a codon.
Sequencing variant TCGA-RQ-AAAT-01A-11D-A38X-10 chr23:118717087 A>C did not map to a codon.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr23:118708861 A>C did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr2:181846843 A>T maps to NM_182678.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr6:90062276 G>A maps to NM_016021.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:21965297 C>G maps to ENST00000458578 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:74392248 G>A maps to NM_022066.3 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:64672477 A>G maps to ENST00000371077 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:25616843 T>A maps to NM_000462.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr11:118242323 A>G maps to NM_004788.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:118253435 T>C maps to NM_004788.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:10211587 G>A maps to NM_001105562.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:56591531 T>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:42613297 T>C maps to NM_015255.2 H793H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:170684547 G>A maps to ENST00000442603 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:19403330 G>A maps to ENST00000375267 N5151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:19467321 G>A maps to ENST00000375267 S2851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:19518854 T>C maps to ENST00000375267 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:19447881 G>A maps to ENST00000375267 G3314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:19500087 A>G maps to ENST00000375267 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:19491322 A>T maps to ENST00000375267 L1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr8:103269902 C>T maps to NM_015902.4 W2715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:42284950 A>G maps to NM_014233.2 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:26608852 G>A maps to NM_183008.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr8:59358555 G>A maps to NM_001077619.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr8:59329406 A>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:134404336 G>A maps to NM_031432.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:165859481 T>C maps to NM_012474.4 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:73717262 G>A maps to NM_003356.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:161123900 C>G maps to NM_016406.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:128870783 A>G maps to NM_020120.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr2:234638242 C>T maps to NM_019093.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:70078392 C>T maps to NM_001073.1 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:70361162 T>C maps to NM_021139.2 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr4:70361333 A>C maps to NM_021139.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CW-01A-11D-A382-10 chr4:69978318 G>A maps to NM_001074.2 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:35957461 G>A maps to NM_152404.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr5:35965610 A>G maps to NM_152404.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:36049323 G>A maps to NM_174914.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:6413639 G>A maps to NM_152896.1 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr9:6413642 G>A maps to NM_152896.1 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132404100 C>T maps to NM_003565.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:132404109 C>T maps to NM_003565.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr16:20352531 G>A maps to ENST00000424589 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:43536046 C>T maps to NM_173568.3 N937N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:43531344 G>A maps to NM_173568.3 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr21:43543097 C>T maps to NM_173568.3 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr21:43557636 C>T maps to NM_173568.3 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr21:43547121 C>T maps to NM_173568.3 Y1228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr19:17751346 G>A maps to ENST00000428389 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr9:35399644 G>T did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr17:73838638 C>T maps to ENST00000412096 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr17:33497207 C>T maps to NM_173167.2 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:33475425 C>T maps to NM_173167.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:176305522 C>T maps to NM_133369.2 H689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr10:73053315 C>T maps to NM_170744.3 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:73039593 C>T maps to NM_170744.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:96140150 C>T maps to NM_003728.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:18958561 A>T maps to ENST00000418384 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr13:115057218 A>G maps to NM_023011.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr13:115067418 G>A maps to NM_023011.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:45683308 C>T maps to NM_006953.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr7:76143284 A>G maps to NM_030570.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:158977927 A>C maps to NM_001135098.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:46775855 C>A maps to NM_006004.2 C37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:229783327 G>C maps to NM_014777.2 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:229783360 C>T maps to NM_014777.2 I1337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:43917603 C>T maps to NM_001077663.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:126207048 G>A maps to NM_001165974.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:17527385 A>G maps to NM_153676.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr11:17552706 C>A maps to NM_153676.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:216363589 C>T maps to ENST00000366943 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:17367353 G>A maps to NM_031941.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:17367353 G>A maps to NM_031941.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:84778260 G>A maps to NM_005153.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr23:47092476 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47107037 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:47092422 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:11995003 C>T maps to NM_201402.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:119243611 T>C maps to NM_004205.4 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:119243911 C>T maps to NM_004205.4 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:55589174 C>T maps to NM_015306.2 A1407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:55563348 G>A maps to NM_015306.2 S1879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr21:17172111 C>T maps to ENST00000285681 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr21:17181167 T>G maps to ENST00000285681 L274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:132161158 G>A did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:57640528 A>G maps to NM_020903.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr15:63855189 G>A maps to NM_006537.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:77921012 A>G maps to NM_020798.2 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:76823424 G>T maps to NM_025090.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:219360655 T>C maps to NM_020935.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:85843347 C>T maps to NM_006590.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:95927171 A>G maps to NM_032147.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:53494282 G>A maps to NM_022832.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:22084200 A>G maps to NM_032236.5 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr1:22033019 C>T maps to NM_032236.5 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:50836845 G>C maps to ENST00000456636 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:75258557 G>A maps to NM_152586.3 T1628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:5039137 C>T maps to NM_004505.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:5039137 C>T maps to NM_004505.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:9057082 G>A maps to NM_003470.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:8989510 C>T maps to NM_003470.2 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:41056721 T>A did not map to a codon.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:41075217 T>G did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:129045814 G>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr12:101674925 T>G maps to NM_014503.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:101767223 C>T maps to NM_014503.2 A2308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr12:101779434 T>C maps to NM_014503.2 L2711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr6:145148755 A>G maps to NM_007124.2 Q3181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:4431879 C>T maps to NM_138440.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:4431372 G>C maps to NM_138440.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:136640121 G>A maps to NM_001134398.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:7811759 C>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:6451833 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:8434345 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr5:133328002 A>G maps to NM_003374.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:219313992 A>C maps to NM_007127.2 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:42568934 C>T maps to NM_004624.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr7:158935180 T>C maps to ENST00000402066 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:36970363 A>G maps to NM_053276.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr2:37035631 C>T maps to NM_053276.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr16:31106014 C>T maps to ENST00000319788 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TV-01A-11D-A382-10 chr23:150573448 C>G did not map to a codon.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:150573425 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr6:133004280 A>G maps to NM_004666.2 *514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:133073843 C>T maps to NM_004665.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr6:133073843 C>T maps to NM_004665.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:51458203 G>A maps to ENST00000273612 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr9:79875040 A>T maps to ENST00000376646 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:79875103 A>G maps to ENST00000376646 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:79959196 G>A maps to ENST00000376646 E2385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr8:100789119 C>T maps to NM_017890.3 C2480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr8:100829994 G>A maps to NM_017890.3 L2800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr1:12429610 C>T maps to NM_015378.2 D3554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VB-A8QN-01A-11D-A382-10 chr1:12398336 C>T maps to NM_015378.2 N2867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr15:41192539 C>T maps to NM_020857.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:122720422 G>A maps to NM_022916.4 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:91550231 G>A maps to NM_018668.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:46706251 C>T maps to NM_018206.4 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr13:52997750 G>A maps to NM_016075.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr6:33234453 G>A maps to NM_022553.4 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:33236825 A>G maps to NM_022553.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:58350339 T>C maps to NM_001130480.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr23:107320446 C>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:65242156 G>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr23:65253453 C>A did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:74707910 C>T maps to NM_182894.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr14:68141104 C>T maps to NM_006370.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:116049198 C>T maps to NM_198496.1 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:116045992 G>A maps to NM_198496.1 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:22144376 C>A maps to NM_173615.3 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:98797659 C>T maps to NM_144992.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr11:61048186 G>A maps to NM_152718.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:61048321 G>C maps to NM_152718.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:61053894 G>A maps to NM_152718.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr12:6076732 G>T maps to NM_000552.3 T2602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:6103280 A>T maps to NM_000552.3 T2115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr12:6172137 G>A maps to NM_000552.3 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:48547155 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:48546836 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr7:123349250 T>C maps to NM_003941.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:41639376 C>T maps to NM_007187.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr13:41639376 C>T maps to NM_007187.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:71142239 G>A maps to NM_022479.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr7:71177022 G>A maps to NM_022479.1 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:73254870 A>G maps to NM_152559.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr4:85612822 T>C maps to NM_014991.4 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:122610982 G>T maps to NM_018117.11 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:122668180 T>C maps to NM_018117.11 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:9511491 C>T maps to NM_145054.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr16:735416 G>C maps to ENST00000248142 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:224607295 T>C maps to NM_025160.6 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:116085147 A>C maps to NM_001012361.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:128528507 C>T maps to NM_018383.4 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:131398632 C>T maps to NM_052844.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:110432840 T>C maps to NM_139281.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr21:44273690 G>A maps to NM_018669.4 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr5:76728995 T>C maps to NM_018268.2 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:76728995 T>C maps to NM_018268.2 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:80573887 G>A maps to NM_019613.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:140048791 C>A maps to NM_017706.4 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TQ-01A-11D-A382-10 chr1:241842831 C>T maps to NM_144625.4 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:43638435 G>T maps to NM_001195831.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:43675538 G>A maps to NM_001195831.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:43638435 G>T maps to NM_001195831.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:67327985 C>G did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:708307 G>A maps to NM_145294.4 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr16:716970 C>T maps to NM_145294.4 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:705343 C>A maps to NM_145294.4 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:90274755 C>T maps to NM_020212.1 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:90281380 T>C maps to NM_020212.1 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr16:683546 G>A maps to NM_053284.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:48913351 G>A maps to NM_175575.5 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr17:48917383 G>A maps to NM_175575.5 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr17:48918274 C>T maps to NM_175575.5 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr15:83499808 C>T maps to NM_001080435.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:1985667 G>A maps to NM_005663.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr17:66423339 G>T maps to NM_017983.5 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr17:66449071 G>A maps to NM_017983.5 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:5257638 G>A maps to NM_015610.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr9:96024181 G>C maps to ENST00000297954 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:54265468 C>T did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr7:120969824 C>A maps to NM_057168.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:22446767 G>A maps to NM_030761.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr10:102242029 G>A maps to NM_003393.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr10:102241723 G>A maps to NM_003393.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:228109695 G>A maps to NM_003395.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:228113072 C>G maps to NM_003395.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr17:44953636 G>A maps to NM_003396.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:30954337 C>T maps to NM_000553.4 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:118474237 G>A maps to ENST00000441406 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr17:6012954 G>A maps to NM_015253.1 W293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr12:108641798 G>A maps to ENST00000261400 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr11:32456396 G>A maps to NM_024426.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr4:184192230 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:10085226 T>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:10106970 C>T did not map to a codon.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr23:10085581 G>A did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:10085226 T>C did not map to a codon.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:10085601 A>C did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:87414307 A>G maps to NM_007013.3 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr8:87473472 T>C maps to NM_007013.3 N840N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:149290780 T>G maps to NM_001168278.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:7684501 G>A maps to NM_020196.2 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:7692131 G>A maps to NM_020196.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:31598338 G>C maps to NM_000379.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:31588394 C>T maps to NM_000379.3 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:31593229 C>T maps to NM_000379.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr2:31606681 A>G maps to NM_000379.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:39225548 G>C maps to NM_194293.2 P1796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:39228773 G>A maps to NM_194293.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr3:39230657 G>A maps to NM_194293.2 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:168104678 T>G maps to NM_152381.5 T2259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:168099554 C>T maps to NM_152381.5 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:28290131 T>C maps to NM_018053.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:28290154 G>A maps to NM_018053.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:43514381 A>G maps to NM_020750.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr8:21856272 C>T maps to ENST00000434536 R794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:180772707 T>C maps to NM_004736.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:180804032 C>T maps to NM_004736.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr7:152346253 C>A maps to NM_005431.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr3:142090121 C>T maps to NM_019001.3 V1009V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr17:48431145 G>A maps to NM_022167.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr11:102094423 C>T maps to NM_001130145.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr1:33246708 T>C maps to NM_003680.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr1:43149083 T>C maps to NM_004559.3 V59V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GS-A9TZ-01A-11D-A38X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr14:75248626 T>C maps to ENST00000423680 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:112871457 C>G maps to NM_022828.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:74076503 G>A maps to NM_180990.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:72913919 C>T maps to NM_175907.4 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr18:72914060 G>A maps to NM_175907.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr3:167045778 G>A maps to ENST00000307529 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr3:167033614 A>G maps to ENST00000307529 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CR-01A-11D-A382-10 chr23:2408512 G>A did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr23:2408433 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:111312964 A>T maps to NM_024508.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50278587 C>T maps to NM_014838.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:50279748 C>T maps to NM_014838.2 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:56189955 C>T maps to NM_030776.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr20:56191474 C>T maps to NM_030776.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:101370090 C>T maps to NM_014415.3 Q1027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr11:114027085 C>T maps to NM_001018011.1 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr1:16272336 T>A maps to ENST00000444654 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr3:114070300 G>C maps to NM_001164342.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr3:114058007 G>T maps to NM_001164342.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:173839434 G>A maps to NM_001122770.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr12:57397249 G>C maps to NM_014830.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:7365288 A>T maps to NM_020899.3 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:22816686 A>G maps to NM_014870.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8046-01A-11D-2210-10 chr18:45566797 G>A maps to NM_001039360.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:45566902 T>C maps to NM_001039360.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr1:33116070 G>A maps to NM_178547.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HO-01A-11D-A31X-10 chr1:37948366 C>T maps to NM_025079.2 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:110007833 T>C maps to NM_033390.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr13:46584499 G>A maps to ENST00000242848 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr13:46543188 G>A maps to ENST00000242848 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr14:89042231 G>A maps to NM_024824.4 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:47575290 A>G maps to NM_015168.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:47584868 C>T maps to NM_015168.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:47572394 C>T maps to NM_015168.1 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:138713673 C>G maps to NM_080660.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:129663532 G>A maps to NM_016478.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr7:129664300 T>C maps to NM_016478.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:64139050 T>C did not map to a codon.
Sequencing variant TCGA-GS-A9U3-01A-11D-A38X-10 chr23:64141832 C>T did not map to a codon.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr23:117959874 A>G did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:103359333 C>T did not map to a codon.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:279184 C>T maps to NM_033089.6 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:37304231 C>T maps to NM_032226.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr12:122975092 C>T maps to NM_017612.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr5:80604426 C>T maps to NM_032280.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:99998749 G>A maps to NM_017984.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr3:28476648 T>G maps to NM_001040432.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:207170025 T>C maps to NM_020923.1 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:207170241 T>C maps to NM_020923.1 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr2:207174558 A>G maps to NM_020923.1 K1769K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:67440288 C>T maps to NM_013304.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr6:158074640 G>A maps to NM_024630.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr16:85024161 G>A maps to NM_001145548.1 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr2:145157592 T>C maps to NM_014795.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr2:145274843 C>T did not map to a codon.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr12:72022728 A>G maps to NM_144982.4 D1305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr12:72020102 G>A maps to NM_144982.4 D1418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr12:72038797 G>A maps to NM_144982.4 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:72992625 C>T maps to NM_006885.3 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:72992628 C>T maps to NM_006885.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr16:72993396 C>T maps to NM_006885.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4XK-01A-11D-A31X-10 chr8:77690571 T>C maps to NM_024721.4 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr8:77618777 G>T maps to NM_024721.4 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr19:44832833 T>A maps to ENST00000412927 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr19:57065995 G>A maps to NM_020828.1 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr14:69259597 C>T did not map to a codon.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr9:115818842 G>A maps to NM_003408.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr4:188924449 A>G maps to NM_174900.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:36884650 C>A maps to NM_133466.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:24229463 C>T did not map to a codon.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr23:24229365 G>A did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr5:79741085 A>G maps to NM_014733.3 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr5:79735831 C>T maps to NM_014733.3 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:41105978 C>G maps to NM_001077268.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:52705173 A>G maps to NM_004799.2 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr1:52803594 C>T maps to NM_004799.2 N1274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr20:62339958 C>G maps to NM_032527.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr8:124265675 C>T maps to NM_007222.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr8:123964010 G>A maps to NM_014943.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr8:123965192 C>T maps to NM_014943.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TU-01A-11D-A382-10 chr3:147128807 C>T maps to NM_003412.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:136649635 C>G did not map to a codon.
Sequencing variant TCGA-GR-A4D6-01A-11D-A31X-10 chr7:99631549 G>T maps to NM_003439.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:28213526 C>T maps to NM_019110.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr10:81053247 G>A maps to NM_020338.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr13:20641391 G>A maps to NM_001190965.1 K1105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr23:70462019 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:35454114 A>G maps to NM_007167.3 Y856Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:21909547 A>G maps to NM_173531.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:21910620 A>G maps to NM_173531.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D9-01B-11D-A31X-10 chr19:21948513 C>A maps to NM_173531.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:64168640 A>G maps to NM_016220.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr5:43173540 C>T maps to ENST00000509156 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:58213742 G>A maps to NM_001085384.1 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47272479 G>A did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47272969 A>G did not map to a codon.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr3:44612047 C>G maps to NM_018651.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:45001397 G>A maps to NM_013256.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr19:35232116 C>T maps to ENST00000392232 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr9:104170418 G>A maps to NM_003452.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr6:28195520 A>G maps to ENST00000425468 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr6:28195520 A>G maps to ENST00000425468 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:12244655 C>T maps to NM_021143.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr11:123599896 G>A maps to NM_003455.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3169320 C>T maps to NM_001042428.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr17:30677324 G>A maps to ENST00000394679 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:58153464 T>A maps to NM_006385.3 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:148947563 C>T maps to NM_012256.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3188788 G>A maps to NM_001134655.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr20:52198618 C>A maps to NM_006526.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:52192416 C>T maps to NM_006526.2 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr20:52193541 C>T maps to NM_006526.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:44536396 T>C maps to NM_001129996.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr19:44571009 A>G maps to NM_013361.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8043-01A-11D-2210-10 chr19:44605365 G>T maps to NM_013398.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:44514421 C>T maps to NM_006300.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:44661731 C>T maps to NM_006630.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr18:74606987 C>T maps to NM_007345.3 N477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:244217661 T>C maps to NM_205768.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:38241219 T>C maps to NM_145011.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:24310073 T>C maps to NM_203282.2 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:22256346 G>A maps to NM_033468.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:22271295 G>A maps to NM_033468.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:57723181 C>T maps to NM_003417.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A82F-01A-11D-A382-10 chr16:89790055 C>T maps to NM_001113525.1 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:89790019 C>T maps to NM_001113525.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:200378494 C>T maps to NM_012482.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:44590752 T>C maps to NM_001037813.2 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:44890650 G>A maps to NM_152354.3 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:44891008 C>T maps to NM_152354.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr21:43413157 C>T maps to NM_020727.4 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:28963860 G>C maps to NM_001010877.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr6:43305990 A>T maps to NM_014345.2 V1915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr16:58032031 G>T maps to NM_020807.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:58031995 G>A maps to NM_020807.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A68N-01A-11D-A31X-10 chr16:58030540 C>T maps to NM_020807.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr19:58983106 G>A maps to NM_014347.2 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:14829344 C>T maps to NM_032433.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr20:25656945 C>T maps to NM_015655.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr10:38345454 A>G maps to NM_006954.1 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr10:38345454 A>G maps to NM_006954.1 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr20:32376747 C>T maps to ENST00000375200 H644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr20:32376747 C>T maps to ENST00000375200 H644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:178139378 C>G maps to NM_005649.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:178309734 A>C maps to NM_058230.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr5:178503471 C>T maps to NM_014594.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr1:33764616 C>T maps to NM_152493.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr9:99180101 C>T maps to NM_153695.3 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr18:72344201 T>C maps to NM_017757.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr18:72346700 T>C maps to NM_017757.2 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr23:47308508 A>C did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:58420415 G>A maps to NM_152475.2 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:58437622 A>G maps to NM_133460.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:58437628 T>A maps to NM_133460.1 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:58437790 A>G maps to NM_133460.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:37618156 T>C maps to NM_144689.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr7:148801429 C>T maps to NM_001001661.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:9639709 T>C maps to NM_024106.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:21991662 A>G maps to NM_003423.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12127369 G>A maps to NM_001080411.1 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:12126127 C>T maps to NM_001080411.1 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr16:3433529 A>G maps to ENST00000396852 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr10:31138093 T>G maps to NM_182755.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:12462872 C>A maps to NM_030824.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:12461744 A>G maps to NM_030824.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:56669888 G>A maps to NM_018337.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr3:44488624 C>A maps to NM_181489.5 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:58991074 C>T maps to NM_017908.2 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr23:134494877 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:57802781 C>T maps to NM_006635.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:57802115 C>T maps to NM_006635.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:37130418 G>A maps to NM_153257.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr9:109689972 G>T maps to NM_021224.4 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:109692819 A>G maps to NM_021224.4 L1954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr9:109685747 G>T maps to NM_021224.4 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149462054 G>A maps to NM_207336.1 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr9:114305074 G>A maps to NM_133464.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:20308148 C>G maps to ENST00000428290 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:20308487 G>T maps to ENST00000428290 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:12691496 G>A maps to NM_020714.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr19:12692408 C>T maps to NM_020714.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:22847916 T>C maps to NM_020855.2 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A86F-01A-11D-A382-10 chr1:247492063 G>A maps to NM_032752.1 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr7:99219099 G>A maps to NM_145115.2 G164G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FA-A4XK-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:99521149 T>C maps to NM_014930.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TW-01A-11D-A382-10 chr2:27601206 A>G maps to NM_144631.4 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr18:74091765 C>T maps to ENST00000443185 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8042-01A-11D-2210-10 chr18:14105584 C>T maps to NM_145287.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr18:22805217 G>A maps to NM_015461.2 C888C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr18:22804941 C>T maps to NM_015461.2 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:37038583 T>C maps to NM_001145649.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:52941504 T>C maps to NM_001143939.1 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:31039255 C>T maps to NM_014717.1 N910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TY-01A-11D-A38X-10 chr19:30934651 C>T maps to NM_014717.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:38102954 T>C maps to NM_152606.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:9453159 C>T maps to NM_032497.1 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:9580304 C>T did not map to a codon.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:9721217 G>A maps to NM_152289.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:2917797 A>G maps to NM_173480.2 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A6HN-01A-11D-A31X-10 chr19:37975033 T>C maps to NM_144694.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:37975399 T>C maps to NM_144694.1 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:37975378 G>A maps to NM_144694.1 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8062-01A-11D-2210-10 chr8:125989721 A>G maps to NM_152412.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TZ-01A-11D-A38X-10 chr8:125989682 G>A maps to NM_152412.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A4BB-01A-11D-A31X-10 chr19:44039460 G>T maps to ENST00000458714 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:52375808 A>G maps to NM_032679.2 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:52375853 T>G maps to NM_032679.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:52375906 T>G maps to NM_032679.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:53014491 T>A maps to NM_001099694.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:58371201 C>T maps to NM_032828.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:5085244 G>A maps to NM_032530.1 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:5085805 G>A maps to NM_032530.1 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3486735 G>A maps to NM_152457.1 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:2050150 A>G maps to ENST00000431526 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:58491381 G>A maps to NM_025027.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:116811183 G>A maps to ENST00000374126 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr3:40574394 C>T maps to NM_001098414.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr5:16465441 T>C maps to NM_033414.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr8:144733175 C>T maps to NM_014789.3 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:55994974 G>T maps to NM_033113.2 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-8693-01A-11D-2397-10 chr16:30795075 C>T maps to NM_001080417.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7DS-01A-11D-A382-10 chr23:47919313 G>T did not map to a codon.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:40929086 C>T maps to NM_023070.2 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr1:91404351 A>G maps to NM_201269.1 Y853Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr23:22291941 G>A did not map to a codon.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:11594927 G>A maps to NM_138783.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:11598287 G>C maps to NM_138783.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr9:40784131 A>G maps to NM_033160.5 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:56952614 A>G maps to ENST00000342634 Y711Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:56952614 A>G maps to ENST00000342634 Y711Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G8-6324-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31075363 G>A maps to NM_001172669.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:31075438 G>A maps to NM_001172669.1 C137C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GR-7353-01A-11D-2210-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:23869830 A>C did not map to a codon.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr19:22363816 A>G maps to NM_001001411.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:41006340 T>C maps to NM_152373.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr16:30583566 C>A maps to NM_001024683.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:30582854 G>A maps to NM_145271.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:30616316 A>G maps to NM_138447.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:30616487 G>A maps to NM_138447.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:120165411 G>A maps to NM_001080470.1 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr1:120166527 A>G maps to NM_001080470.1 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:9407467 G>A maps to NM_198535.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-A4D5-01A-11D-A31X-10 chr19:9407193 C>A maps to NM_198535.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr19:12060626 A>G maps to NM_144566.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GS-A9TT-01A-11D-A382-10 chr19:12059330 T>G maps to NM_144566.1 Y164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FA-A7Q1-01A-11D-A382-10 chr8:37555933 C>T maps to NM_025069.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-A7CQ-01A-11D-A382-10 chr8:144775925 C>T maps to NM_173831.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6906-01A-11D-2210-10 chr7:56007497 A>G maps to NM_182633.1 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:20736638 C>T maps to NM_001159293.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr22:20760105 C>T maps to NM_003426.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:149174757 G>A maps to NM_001163474.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:12087920 G>C maps to NM_001012753.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr19:12087920 G>C maps to NM_001012753.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr16:30536797 C>T maps to NM_024671.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6914-01A-11D-2210-10 chr19:2934248 T>C maps to NM_021217.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:40580425 A>G maps to NM_001142577.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:40581676 G>A maps to NM_001142577.1 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:40580544 G>A maps to NM_001142577.1 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:40580425 A>G maps to NM_001142577.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:40541844 A>G maps to NM_001005851.2 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:38160254 A>C maps to NM_152605.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr3:113955725 G>A maps to NM_007136.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr7:127026183 A>C maps to NM_176814.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8061-01A-11D-2210-10 chr2:185463691 G>A maps to NM_194250.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr2:185800767 T>C maps to NM_194250.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7351-01A-11D-2210-10 chr23:47774598 C>T did not map to a codon.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:53994082 T>C maps to NM_001004301.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:58386313 G>A maps to NM_001144989.1 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr19:53456124 G>C maps to NM_001031665.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr20:57766112 G>A maps to NM_178457.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr14:102805555 C>T maps to NM_018335.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:52569478 G>A maps to NM_001136499.1 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8041-01A-11D-2210-10 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6325-01A-11D-2210-10 chr19:23543077 C>T maps to NM_003430.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GR-7353-01A-11D-2210-10 chr19:23544514 A>T maps to NM_003430.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr19:20044885 T>C maps to NM_031218.3 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:20026162 G>C maps to NM_031218.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6909-01A-11D-2210-10 chr19:20044885 T>C maps to NM_031218.3 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr11:60642632 C>T maps to NM_207341.2 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FF-8047-01A-11D-2210-10 chr7:76058884 C>T maps to NM_001110354.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr17:38028634 T>C maps to NM_199321.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr2:135988235 G>A maps to NM_032143.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr16:3140600 C>T maps to NM_032805.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr15:85164529 C>T maps to NM_181877.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FM-8000-01A-11D-2210-10 chr1:33959917 C>T maps to NM_145238.3 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RQ-A6JB-01A-11D-A31X-10 chr1:33956947 C>T maps to NM_145238.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6326-01A-11D-2210-10 chr19:58849788 G>A maps to NM_181846.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6907-01A-11D-2210-10 chr19:13941254 G>A maps to NM_023072.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G8-6324-01A-11D-2210-10 chr1:53262455 G>A maps to NM_024646.2 R495R. Only missense variants will be evaluated by CHASM.
