5874 NP_705833 L340V not found in SNVbox database
50 NP_705833 K280Q not found in SNVbox database
914 NP_705833 G935A not found in SNVbox database
1828 NP_705833 M529V not found in SNVbox database
1881 NP_705833 R222C not found in SNVbox database
2410 NP_705833 G161V not found in SNVbox database
2879 NP_705833 G326S not found in SNVbox database
3050 NP_705833 K492N not found in SNVbox database
3254 NP_705833 V497I not found in SNVbox database
3369 NP_705833 G386R not found in SNVbox database
3383 NP_705833 P517L not found in SNVbox database
4024 NP_705833 H965D not found in SNVbox database
4805 NP_705833 P455L not found in SNVbox database
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:58863736 A>G maps to NM_130786.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:9243976 G>A maps to NM_000014.4 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:12711260 G>A maps to NM_001013630.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr6:44269150 C>G maps to NM_020745.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr6:44270855 C>T maps to NM_020745.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:105967613 C>T maps to NM_015423.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XA-01A-11D-A26M-08 chr17:79094024 G>A maps to NM_001080395.2 D1237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr2:215843554 G>A maps to NM_173076.2 Y1650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:215809801 C>T maps to NM_173076.2 P2422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:48556329 T>C maps to NM_152701.3 T4550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:48411940 A>T maps to NM_152701.3 S3660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr7:48506640 C>T maps to NM_152701.3 Q4302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr16:2374515 G>A maps to NM_001089.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr1:94486866 G>A maps to NM_000350.2 P1649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr1:94528251 G>T maps to NM_000350.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:94512530 G>A maps to NM_000350.2 Y954Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr1:94480118 C>A maps to NM_000350.2 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:67111541 A>G maps to NM_080284.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr19:1042062 G>A maps to NM_019112.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:1044691 C>T maps to NM_019112.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr17:66914236 G>A maps to NM_007168.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr17:66982396 C>T maps to NM_080283.3 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr7:87183088 T>C maps to NM_000927.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr7:87178714 C>T maps to NM_000927.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr1:229685029 C>G maps to NM_012089.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:20767946 G>A maps to NM_001163941.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:74291460 C>A did not map to a codon.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr16:48211012 C>T maps to NM_032583.3 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr16:48174761 G>A maps to NM_033226.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr16:48162528 G>A maps to NM_033226.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr17:48733299 C>T maps to NM_003786.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr13:95840745 G>A maps to NM_005845.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr12:22012588 C>A maps to NM_005691.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr12:22001087 G>A maps to NM_005691.2 D954D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:30558336 C>G maps to NM_001025091.1 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr7:150911220 G>A maps to NM_005692.3 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr21:43708162 C>T maps to NM_004915.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:44050051 G>A maps to NM_022436.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr3:111705807 A>C maps to NM_018394.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr3:100489773 T>C maps to ENST00000471714 Q1509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr7:150554514 C>T maps to ENST00000416793 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr7:150555012 C>T maps to ENST00000416793 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:915190 G>A maps to NM_021962.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr11:34184210 G>A maps to NM_145804.2 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr12:109644645 C>T maps to NM_001093.3 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr12:109690902 C>T maps to NM_001093.3 T1995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr12:112193512 G>A maps to NM_001136538.1 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr12:121176334 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr15:89386880 T>C did not map to a codon.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr1:226349373 G>A maps to NM_022735.3 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:44089248 G>T maps to NM_032592.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr16:67694141 C>T maps to NM_001082486.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr17:61557163 C>T maps to NM_000789.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:15580078 T>C did not map to a codon.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr23:15609936 C>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:6312224 G>A maps to NM_133492.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr14:23550989 C>T maps to NM_014977.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:40030157 G>A maps to ENST00000401700 Q894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr17:40065857 G>A maps to ENST00000401700 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:96747044 C>A maps to NM_020186.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr20:44472286 C>G maps to NM_005469.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:23748658 G>T did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr4:8396381 G>A maps to NM_003501.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr11:47264837 G>A maps to NM_001610.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr3:132051044 C>T maps to NM_001134194.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:70824012 G>A did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr15:78475122 C>T maps to NM_015162.4 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:185724473 C>A maps to NM_001995.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:108921234 C>T did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:108926515 G>C did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr16:20635525 G>A maps to NM_052956.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr16:20476847 C>T maps to NM_001010845.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:20477030 C>T maps to NM_001010845.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr16:20492161 G>A maps to NM_001010845.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr12:7477157 G>A maps to NM_001080454.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr15:35086922 G>A maps to NM_005159.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr2:74146596 C>T maps to NM_001615.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr9:111617664 C>T maps to NM_006686.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:18152413 C>T maps to NM_030812.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr11:66330633 C>T maps to NM_001104.1 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:114699854 C>T maps to NM_005721.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr23:127186135 C>A did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr23:127185375 G>T did not map to a codon.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr2:158443696 A>G did not map to a codon.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr2:158401020 G>A maps to NM_145259.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr4:123336615 A>T maps to NM_139243.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr8:39624671 T>C maps to NM_001464.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr14:70991444 G>A maps to NM_003814.4 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr8:24181516 G>A did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr8:24187574 C>T maps to NM_014265.4 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr8:24201056 A>G maps to NM_014265.4 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr8:24193002 C>T maps to NM_014265.4 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:120437549 G>A maps to NM_021794.2 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr8:39091489 G>C maps to NM_145004.5 V569V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HT-7480-01A-11D-2086-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr8:24350111 T>A did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr8:24350562 A>T maps to ENST00000380789 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr5:33648938 G>A maps to NM_030955.2 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr5:33576464 G>A maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr11:130341227 G>A maps to NM_139055.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr11:130332500 C>T maps to NM_139055.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr15:100657166 G>A maps to NM_139057.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr16:77401349 G>A maps to NM_199355.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr5:129039954 C>A maps to NM_133638.3 G1055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr5:129070794 C>G maps to NM_133638.3 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr12:43840497 G>A maps to ENST00000389420 H699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:73434465 G>C maps to NM_014243.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr15:79092722 G>A maps to ENST00000258883 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr9:18829916 G>A maps to NM_001040272.4 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr9:18776968 C>T maps to NM_001040272.4 D914D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:154560601 G>A maps to ENST00000292205 N1049N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr10:1405303 C>T maps to NM_018702.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:33585651 C>T maps to ENST00000373441 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr7:45717490 G>A maps to NM_021116.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr1:167870981 C>T maps to NM_018417.4 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:167870911 G>A maps to NM_018417.4 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:7520912 C>T maps to NM_020546.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr14:24791274 G>A maps to NM_139247.3 N861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:123036942 G>A maps to NM_183357.2 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:50347882 C>G maps to NM_001114.3 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr8:131922057 G>A maps to NM_001115.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr4:2877686 G>A maps to NM_014189.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr2:70904916 G>C maps to NM_001185054.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr4:100205753 G>A maps to NM_000667.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr4:100205898 C>T maps to NM_000667.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr20:49508436 A>G maps to NM_181442.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr20:4202426 G>T maps to NM_000678.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr2:96781414 C>T maps to NM_000682.5 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:148206921 C>T maps to NM_000024.5 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr1:244581039 T>C maps to NM_001126.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr7:44151919 G>A maps to NM_001129.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:148068961 A>G did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:148069036 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:148037322 C>T did not map to a codon.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:148049221 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:148035252 G>A did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:148037447 A>G did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr2:236626275 G>T maps to NM_001037131.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:58126703 G>A maps to NM_001122772.1 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:75457305 G>A maps to NM_001144000.1 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr10:51769669 C>T maps to NM_001077665.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr15:86838483 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:86800127 G>A maps to NM_152336.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr1:15904230 G>A maps to NM_024758.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:115303725 G>A did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr20:32873404 G>A maps to NM_000687.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr1:27875776 C>T maps to NM_001029882.2 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr6:135787391 G>A maps to NM_017651.4 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr11:62289981 G>A maps to NM_001620.1 D3969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr11:62299209 C>T maps to NM_001620.1 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr14:105420968 C>T maps to NM_138420.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr14:105421332 G>A maps to NM_138420.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr14:105420365 G>A maps to NM_138420.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr5:413499 G>A maps to NM_020731.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr5:423983 C>G maps to NM_020731.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr12:8757942 G>A maps to NM_020661.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr10:71880313 C>T maps to NM_032797.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr1:26650672 C>T maps to NM_001039775.3 W1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:159035846 G>A maps to NM_004833.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr17:6329142 C>T maps to NM_014336.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:6331636 C>T did not map to a codon.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr15:86287024 G>A maps to NM_006738.4 K2791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:49957835 G>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:49957596 A>G did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:49958080 T>C did not map to a codon.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr23:49958836 C>T did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr23:49957503 G>C did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr23:49958223 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr7:91631133 G>T maps to NM_005751.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:91737806 G>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr7:134212704 C>T maps to NM_020299.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr10:5144388 C>T maps to NM_003739.4 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:55042059 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:55052377 G>A did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:58254314 G>A maps to NM_003888.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr15:101425494 C>T maps to NM_000693.2 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr17:19641634 C>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr17:19646620 G>A maps to NM_000691.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr11:67433864 G>A maps to NM_001031615.1 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr1:19209802 G>A maps to NM_003748.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr6:135239870 C>T maps to NM_022568.3 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:110952272 G>C did not map to a codon.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr19:36501794 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:73717090 C>T maps to NM_015120.4 R2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr17:7976178 G>A maps to NM_001139.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr18:56203629 G>A maps to NM_052947.3 D1263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr18:56246387 C>T maps to NM_052947.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr15:85383196 G>A maps to NM_020778.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:85382931 G>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr2:233274353 G>A maps to NM_031313.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:202609062 G>A maps to NM_020919.3 H696H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr2:202619250 G>A maps to NM_020919.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:116840417 C>T maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr11:46563767 C>T maps to ENST00000458649 W600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr11:46431878 C>G maps to ENST00000458649 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr16:56396892 G>A maps to NM_001144.4 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr12:53825208 C>T maps to NM_020547.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr11:118074284 C>G maps to NM_001098526.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:110050352 G>A maps to NM_020703.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:109459854 A>G did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:109444268 T>C did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:112058787 T>C did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:112022265 C>A did not map to a codon.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:115216304 G>A maps to NM_000036.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr17:66246611 G>A did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr12:121769170 G>A maps to NM_016237.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr12:121790074 C>G maps to NM_016237.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr8:108306211 A>G maps to NM_001146.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr9:129854132 C>G maps to NM_012098.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:41554023 C>T maps to ENST00000415018 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:41577304 G>A maps to ENST00000415018 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr4:114278386 T>C maps to NM_001148.4 I2871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr4:114280345 C>T maps to NM_001148.4 T3524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr10:61958112 T>C maps to NM_020987.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr17:4088254 C>G maps to NM_016376.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr5:139917068 C>T maps to ENST00000253810 R2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr7:91981896 C>T maps to NM_019004.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr11:113267964 C>T maps to NM_178510.1 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:241468875 G>A maps to ENST00000401804 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr5:72849255 T>C maps to NM_023039.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr16:89357150 C>T maps to NM_013275.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:89347171 C>T maps to NM_013275.4 P1926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr4:73957065 T>A maps to NM_032217.3 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr4:74012997 T>C maps to NM_032217.3 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr4:74021733 A>G did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr4:73942822 T>C did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr9:42368596 C>T maps to NM_001012421.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:97506179 T>A maps to NM_144994.7 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr19:33096833 A>G maps to NM_032139.2 N800N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr10:37508225 G>T maps to ENST00000374660 E1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr18:14763802 G>A maps to NM_001145029.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr12:56645996 A>G maps to NM_173595.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr12:101437334 T>A maps to ENST00000392977 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr12:45797220 G>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:242148713 C>T maps to NM_001001891.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:429779 G>A maps to NM_001012302.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:69297778 A>G maps to NM_032208.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr9:75773610 C>T maps to NM_000700.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr4:169105804 T>C maps to NM_007193.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr9:33625259 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XA-01A-11D-A26M-08 chr4:79531253 T>C maps to NM_005139.2 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr1:150955564 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:150957081 C>T maps to NM_003568.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr7:36570026 C>A maps to NM_001177506.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr2:201478595 G>A maps to NM_001159.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr17:58179805 T>A did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:986943 C>T maps to ENST00000332231 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr5:115177766 C>T maps to NM_001284.2 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr4:41015609 C>T maps to NM_004307.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr1:159557755 G>A maps to NM_001639.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:55033525 A>T did not map to a codon.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr23:55033115 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:55033741 G>T did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr11:43343604 C>T maps to NM_001142930.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr11:57003347 A>G maps to NM_005161.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr2:21228171 G>A maps to NM_000384.2 I3856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr2:21226161 C>T maps to NM_000384.2 R4044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr2:21227212 G>A maps to NM_000384.2 A4005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:21234702 C>T maps to NM_000384.2 G1679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr2:21230554 A>C maps to NM_000384.2 L3062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr2:21230418 G>A maps to NM_000384.2 N3107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr22:39387536 C>T maps to ENST00000402182 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:45411903 G>A maps to NM_000041.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr22:36587385 G>A maps to ENST00000332987 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:23899065 T>A did not map to a codon.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr3:57291435 A>G maps to NM_012096.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr16:88876923 G>A maps to NM_000485.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr18:24442316 G>A maps to NM_001650.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr5:115351038 T>C maps to NM_173800.4 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr5:115298644 C>T maps to NM_173800.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:66765382 T>C did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:66863187 G>C did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr11:72410501 C>A maps to NM_001040118.2 E800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:143694471 G>A maps to NM_015193.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr15:32917834 G>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:129959562 A>T maps to NM_033515.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr10:49791050 G>A maps to ENST00000417912 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:130217832 C>T did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:153175535 G>A did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:11174685 C>T did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr12:15095521 G>A maps to NM_001175.4 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr19:42396178 C>T maps to NM_199002.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:156916462 G>C maps to NM_198236.1 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr11:120355175 C>T maps to NM_015313.2 C1528C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:8216516 C>T maps to NM_173728.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr7:143884336 C>T maps to NM_001003702.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr2:131797916 C>A maps to NM_015320.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:135825809 C>A did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:135862896 T>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:62917173 T>G did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:62893976 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:62857962 C>T did not map to a codon.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:27101341 G>T maps to NM_006015.4 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:27100380 C>T maps to NM_006015.4 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr1:27056285 C>T maps to NM_006015.4 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr6:157495230 C>T maps to ENST00000367148 Q1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr6:157454204 T>A maps to ENST00000367148 Y792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr12:46242661 C>T maps to NM_152641.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr6:109294620 T>C maps to NM_032131.4 H836H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr10:23292318 C>T maps to NM_173081.3 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr16:31470907 G>A maps to ENST00000408912 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr19:19162909 C>T maps to ENST00000392336 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:100808651 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:100910838 T>A did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:100912541 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:101857470 T>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr11:13402767 T>C maps to ENST00000403290 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr3:35758846 T>C maps to ENST00000458225 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:69500074 G>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:4619833 G>C maps to ENST00000412477 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:2836027 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr23:2853193 C>A did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:2867630 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:3021882 C>T did not map to a codon.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr11:3681543 C>T maps to NM_004314.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr4:77018806 C>T maps to NM_001130016.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr4:77018800 A>G maps to NM_001130016.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:19960525 G>A maps to NM_001670.2 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr10:104650299 G>A did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr2:239344636 C>A maps to NM_001040445.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr15:101170213 C>T maps to NM_198243.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:15272892 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:1551212 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:1536975 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:95228796 G>A maps to NM_017680.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr3:130732930 C>T maps to ENST00000514044 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:119413977 G>A maps to ENST00000313400 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr2:25972672 C>T maps to NM_018263.4 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr2:23985166 C>G maps to NM_017552.1 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr1:1431190 G>T maps to NM_031921.4 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr1:1386074 C>T maps to NM_001039211.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:32088574 G>A maps to NM_004381.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr12:14634096 T>C maps to NM_018179.3 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr16:10551309 G>T maps to NM_024997.2 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr11:64677553 C>A maps to ENST00000421419 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr11:64665786 C>T maps to ENST00000421419 G1575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:96757938 A>G maps to NM_018036.5 H1859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr6:106764058 G>A maps to NM_004849.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:220088459 G>A maps to NM_024085.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:216209587 C>T maps to NM_004044.6 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr12:7050145 C>T maps to NM_001940.3 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr5:160039780 G>A maps to NM_025153.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr5:160049523 G>T maps to NM_025153.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:138850562 T>A did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:138857057 T>C did not map to a codon.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:138886674 G>C did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr3:194170982 G>A maps to NM_024524.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:160136481 C>T maps to NM_144699.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr3:10452377 C>T maps to NM_001001331.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:152813392 C>T did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:152845600 C>T did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:152827613 G>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:152807341 G>A did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr19:36046428 G>C maps to NM_000704.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr19:36045931 C>T maps to NM_000704.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:36046392 C>T maps to NM_000704.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr12:57036471 G>C maps to NM_001686.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:81613926 G>A maps to NM_001017971.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:77301815 T>G did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr13:26411308 C>A maps to NM_016529.4 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr13:26125549 C>A maps to NM_016529.4 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr13:26273414 G>A maps to NM_016529.4 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:1785265 G>A maps to NM_138813.2 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr19:1785227 G>A maps to NM_138813.2 Y1154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:1785488 G>A maps to NM_138813.2 C1124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr18:77134066 C>T maps to NM_198531.3 Y1080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr10:117061533 G>A maps to NM_207303.2 W933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr23:76829759 G>C did not map to a codon.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr23:76939963 G>A did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr23:76940082 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr23:76855198 A>G did not map to a codon.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:76940499 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:76888812 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:76939873 G>A did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr23:76890085 T>C did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:76949413 A>G did not map to a codon.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr23:76845410 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:76764101 G>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:76813105 T>G did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr23:76874370 A>C did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr23:76874432 A>C did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr23:76814312 G>A did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:76813013 C>A did not map to a codon.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr23:76814187 A>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:76940086 T>C did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:76938406 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr23:76875910 T>C did not map to a codon.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr23:76814312 G>A did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:76939495 G>A did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:76813114 C>T did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:76889171 A>T did not map to a codon.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr23:76912103 G>C did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr23:76939521 A>T did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:76937356 T>C did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:76845301 A>G did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr23:76855964 A>C did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr23:76813075 T>C did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr23:76940499 T>G did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr23:76813081 A>G did not map to a codon.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr23:76849220 T>C did not map to a codon.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr23:76814318 T>C did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr23:76940488 T>A did not map to a codon.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:76890082 A>C did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:76849220 T>C did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:76813057 C>T did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:76937899 T>A did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:76938787 G>T did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:76849195 A>G did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:76939234 C>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:76931744 T>C did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:76890194 C>G did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:76937080 C>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr23:76938919 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:76939696 C>A did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:76940430 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:76939960 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr23:76937037 G>C did not map to a codon.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr23:76938787 G>A did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr12:111908029 A>G maps to NM_002973.3 Y1066Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr16:28847393 A>G maps to NM_148414.1 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr16:28846973 T>C maps to NM_148414.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:13337541 T>C did not map to a codon.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr19:57744017 C>T maps to NM_001015878.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr12:63543860 C>T maps to NM_000706.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:153172154 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr17:63533497 G>A maps to NM_004655.3 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr3:182987918 G>A maps to NM_032047.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr12:665814 C>T maps to NM_173593.3 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:33135342 G>A maps to NM_001497.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr6:90661004 G>A maps to NM_001170794.1 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr10:121432113 G>A maps to NM_004281.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:70048900 C>T maps to NM_001704.2 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr20:17716422 C>T maps to NM_001159495.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr5:17275507 C>T maps to NM_006317.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr19:49459500 C>T maps to NM_138761.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:123664897 A>G maps to NM_152618.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr17:58967053 A>G did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr2:60679727 C>T maps to NM_018014.3 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr14:99641423 C>T maps to NM_138576.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr22:18185019 T>G maps to NM_015367.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:39923698 C>T did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:39932303 G>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:39933842 G>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:39933841 C>T did not map to a codon.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr23:39934220 C>G did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:39931689 G>A did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr23:39932879 G>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:129147462 G>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr22:23631728 C>G maps to NM_004327.3 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr14:101005289 C>T maps to NM_020836.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:18221652 G>T did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr23:18234678 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr23:18183207 G>A did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:18189325 T>A did not map to a codon.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr6:107391125 G>A maps to NM_001080450.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr11:61724344 T>C maps to NM_001139443.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:12866568 C>T maps to NM_017682.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:70048983 G>A maps to NM_032735.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:152770258 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:152773770 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr9:95481528 C>T maps to NM_001003800.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr19:53793156 C>T maps to NM_033341.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr8:11414293 C>T maps to ENST00000427279 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr1:169347581 A>G maps to NM_003666.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:22037986 C>T maps to NM_006129.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:79792135 A>G maps to NM_198892.1 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:79793823 G>A maps to NM_198892.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr6:7727730 G>A maps to NM_001718.4 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr10:88679127 C>T maps to NM_004329.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:172578698 T>C did not map to a codon.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr5:172587004 G>A maps to NM_013979.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:36953196 C>T maps to NM_001725.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:36952336 C>T maps to NM_001725.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr1:220240685 T>C maps to NM_006085.4 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr14:105688183 G>A maps to NM_001519.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr3:9781282 C>T maps to NM_001003694.1 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:135574305 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:135572457 G>T did not map to a codon.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr23:79932311 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:79942475 A>G did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr1:32842100 G>T maps to NM_001143888.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:49699984 C>T maps to NM_003458.3 S3569S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr1:92606708 G>T maps to NM_183242.3 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr3:15686763 C>A maps to NM_000060.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:100613412 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:100615677 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:32362766 G>A maps to ENST00000468270 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr10:103281442 G>A maps to NM_033637.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr2:111398885 G>A maps to NM_004336.3 N927N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr15:40509801 C>T maps to ENST00000412359 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr17:56402927 C>T maps to NM_004758.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr10:120489878 C>T maps to NM_153810.4 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr10:33134207 A>G maps to ENST00000375025 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:122774731 G>A maps to NM_024806.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr11:82644344 A>G maps to NM_145018.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr11:82643882 A>T maps to NM_145018.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr12:40041652 C>A maps to NM_001031748.2 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr12:112617094 G>C maps to NM_001109662.2 V3526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr12:112647837 G>A maps to NM_001109662.2 A2444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:64746732 G>C maps to NM_001170633.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:97082741 G>A maps to ENST00000342887 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr14:76668099 G>A maps to NM_017926.2 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr14:50472372 G>A maps to NM_001012706.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr14:95932396 C>T maps to NM_152592.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr15:24924469 T>A maps to NM_018958.2 C1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr15:24921604 C>T maps to NM_018958.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr15:24921091 T>A maps to NM_018958.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr15:34646896 C>A maps to ENST00000438749 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr16:81095241 C>A maps to NM_152337.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr16:89785501 G>A maps to NM_004913.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:67701891 A>G maps to NM_001012984.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:19726119 C>A maps to NM_001012991.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr17:72959891 C>T maps to NM_030630.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr18:13645352 G>A maps to NM_181481.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:12841861 G>A maps to NM_024038.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr19:50981246 C>G maps to ENST00000376920 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr2:68270035 T>G maps to ENST00000407324 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr1:200880751 C>T maps to NM_018265.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr1:200880682 C>T maps to NM_018265.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr1:169394120 G>A maps to ENST00000367806 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr1:57185711 A>G maps to NM_001004303.4 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:75038486 A>C maps to NM_001002912.4 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr1:206243207 G>A maps to NM_001007544.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:3236734 G>A maps to NM_001009984.1 Q1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:61428540 C>G maps to NM_018270.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:18794626 G>A maps to NM_178483.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr2:27804532 T>C maps to NM_032266.3 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr2:27799837 A>T maps to NM_032266.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:27438347 G>A maps to NM_080592.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr2:106690447 C>G maps to NM_032411.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr2:27360156 G>A maps to NM_178553.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:219232560 C>T maps to NM_198559.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:29295045 G>A maps to NM_001029883.1 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr19:6686852 G>A maps to NM_000064.2 Q1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:6678248 G>T maps to NM_000064.2 I1588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:6697495 G>A maps to NM_000064.2 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr19:6709692 A>G did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr3:119465993 C>T maps to NM_033364.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr3:184870437 G>A maps to NM_001025266.1 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:123812512 C>T maps to NM_001735.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr5:134782789 G>A maps to NM_130848.2 Y3Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr5:175763803 A>C maps to ENST00000443967 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:43506029 C>T maps to NM_198566.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr5:43488035 T>C maps to NM_198566.2 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr5:41149346 A>G maps to NM_001115131.1 C873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr5:41149448 G>A maps to NM_001115131.1 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:41159280 G>A maps to NM_001115131.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:32261387 C>T maps to ENST00000447241 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr6:43193849 C>T maps to ENST00000509253 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:30618836 G>T maps to NM_001161376.1 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr7:142637544 G>A maps to NM_178829.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:129856217 C>T maps to NM_145268.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr7:120629720 C>T maps to NM_024913.4 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr7:120629720 C>T maps to NM_024913.4 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr1:57417780 C>T maps to NM_000066.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr8:42401644 C>T maps to NM_001135675.1 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr8:27891082 G>T maps to ENST00000341513 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr5:39364518 T>A maps to NM_001737.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:112963590 C>T maps to NM_001012993.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr9:34381049 G>A maps to NM_032596.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr19:49143393 G>A maps to NM_001217.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr8:86180768 A>G maps to NM_198584.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:24479227 G>A maps to NM_012295.3 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr18:20837288 C>T maps to NM_001100619.2 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr11:67287315 G>A maps to NM_016366.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr9:140946555 G>A maps to ENST00000277549 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr9:140946549 C>G maps to ENST00000277549 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr1:181707519 C>T maps to ENST00000357570 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:49088175 G>A did not map to a codon.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr23:49063293 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:49088266 G>A did not map to a codon.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr17:48669422 C>T maps to NM_018896.3 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr17:48703622 A>G maps to NM_018896.3 L2215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:48652950 G>A maps to NM_018896.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:1250282 G>A maps to NM_021098.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr7:81624210 G>A maps to NM_000722.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr3:50417430 C>T maps to ENST00000435965 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr3:55052338 C>T maps to NM_018398.2 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr12:1995490 G>A maps to NM_172364.4 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr2:27447692 G>A maps to NM_004341.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr3:85984925 C>G maps to NM_153184.3 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:121965554 C>G maps to NM_001167940.1 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr7:93072937 C>G maps to NM_001164737.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:188225388 T>G maps to NM_005795.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr4:114436308 G>A maps to ENST00000515496 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr9:138713008 G>A maps to ENST00000409386 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr2:30966406 C>T maps to ENST00000295055 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:223900425 C>G maps to NM_001748.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr16:55600781 A>G maps to NM_032330.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:75692507 G>A maps to NM_032606.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:41393958 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr17:73498547 C>G maps to NM_020753.3 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:73502704 G>T maps to NM_020753.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr11:104915358 G>A maps to NM_001017534.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr3:122003578 G>A maps to NM_001178065.1 Q936Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:88958663 C>T maps to NM_005187.5 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr19:45284224 C>T maps to NM_012116.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr20:54573804 G>A maps to NM_080617.4 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr20:54579017 C>T maps to NM_080617.4 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr21:37518617 G>A maps to NM_001236.3 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr9:70182124 A>G did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr18:57136831 G>A maps to NM_133459.3 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr3:42907139 A>G maps to NM_001296.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr3:42906980 C>T maps to NM_001296.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr2:219895548 G>A maps to NM_194302.2 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:219900290 C>T maps to NM_194302.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:219868813 C>T maps to NM_194302.2 K1805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr16:58292427 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr16:58287906 A>G maps to NM_014157.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr22:21988387 C>T maps to NM_152612.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:42221754 C>A maps to NM_024821.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr17:18454999 G>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr4:24875311 T>C maps to NM_001130726.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr4:77250101 G>A maps to NM_001042784.1 H983H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:77255305 A>T maps to NM_001042784.1 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr4:77317544 A>G maps to NM_001042784.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:11462649 G>A did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:133379652 C>T did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:49105640 C>T did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr1:3677957 C>G maps to NM_152492.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr15:74554907 C>T maps to ENST00000321288 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr15:74623085 G>A maps to ENST00000321288 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:94769687 G>A maps to NM_001042399.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr16:3085392 G>A maps to NM_001103175.1 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr5:150565606 G>A maps to NM_015621.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr13:52439603 G>A maps to NM_031290.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:46915401 G>A maps to NM_032040.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr11:64112394 G>A maps to NM_032251.5 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:91806239 G>A maps to NM_001080414.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr9:36170044 C>A maps to NM_005893.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:26483466 G>A maps to NM_000730.2 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr11:6292256 C>T maps to NM_176875.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:32612838 C>T maps to NM_002986.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:50051783 G>A did not map to a codon.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr23:50055580 T>A did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr4:78081990 A>T maps to NM_004354.2 K132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr5:159707583 G>A maps to NM_024565.5 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr12:49087564 C>A maps to NM_001240.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr17:38711758 G>A maps to NM_001838.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr17:38711203 G>A maps to NM_001838.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr3:45942528 C>T maps to NM_031200.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr2:73478418 C>G maps to NM_006429.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:74472142 G>A maps to NM_133493.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:74491007 T>C maps to NM_133493.3 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr12:7635287 G>A maps to NM_004244.4 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr12:7527056 G>A maps to ENST00000416109 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr12:7526162 G>A maps to ENST00000416109 N1171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr1:158226759 C>T maps to NM_001763.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr1:158299223 C>T maps to NM_001764.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr3:112064082 C>T maps to NM_001004196.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr19:7809892 G>A maps to NM_021155.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr19:35832000 T>C maps to NM_001771.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:160811430 C>A maps to NM_001166663.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:160811090 G>A maps to NM_001166663.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr1:160811159 G>A maps to NM_001166663.1 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr11:66084108 G>A maps to NM_020404.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr6:47575764 G>A did not map to a codon.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr17:72473593 C>T maps to NM_007261.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr17:72613293 G>A maps to ENST00000426295 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr17:72613302 T>C maps to ENST00000426295 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr17:72521998 C>T maps to NM_174892.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:118211222 C>T maps to NM_000732.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr20:44751285 A>G maps to NM_001250.4 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr5:149782732 G>A maps to NM_001025159.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr11:44640200 G>A maps to NM_002231.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr11:44621760 C>T maps to NM_002231.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr20:23065098 G>A maps to NM_012072.3 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr19:14508024 C>T maps to NM_078481.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:149938822 G>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:100818539 G>T maps to NM_033312.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:43824984 G>A maps to NM_001255.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:43826261 C>A maps to NM_001255.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr5:54436229 G>A maps to NM_001170402.1 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr1:227348327 T>C maps to ENST00000366766 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr14:103430858 G>A maps to NM_006035.3 D902D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr5:21752211 G>A maps to NM_004061.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:21752318 G>A maps to NM_004061.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr16:89261355 G>A maps to NM_004933.2 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr8:95182643 G>A maps to NM_001144663.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr18:59174699 G>A maps to NM_031891.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:44838992 G>A maps to NM_021248.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr14:23523983 C>T maps to NM_022478.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr20:60498708 G>T maps to NM_001794.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:60503308 C>T maps to NM_001794.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:66424459 C>T maps to NM_001795.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr5:31323106 C>T maps to NM_004932.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr5:31323147 G>T maps to NM_004932.2 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:62055207 G>A maps to NM_001796.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:62055201 G>A maps to NM_001796.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr5:26881406 T>G maps to NM_016279.3 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr10:85970773 G>A maps to NM_033100.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:105669000 G>A maps to NM_152750.4 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr1:1635942 A>C did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr7:90377063 T>C maps to NM_012395.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr7:90613504 T>A maps to NM_012395.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr23:47082980 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr9:123342217 A>G maps to NM_018249.4 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:123253596 G>A maps to NM_018249.4 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr23:18646677 C>A did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr12:12871756 A>C did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr14:54884630 C>T maps to NM_005192.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:15510997 C>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:15532458 G>A maps to ENST00000455584 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:31083951 G>A maps to NM_001264.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr16:80718588 G>A maps to NM_152342.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr19:42224878 G>A maps to NM_004363.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr14:23588123 G>A maps to NM_001805.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:46776724 G>A maps to NM_014246.1 R2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:46806346 G>A maps to NM_014246.1 D1627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:109801231 C>T maps to NM_001408.2 H1163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr3:48690584 C>T maps to NM_001407.2 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr3:48684251 G>A maps to NM_001407.2 Y2413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr4:56823425 T>C maps to NM_025009.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr20:34059912 T>C maps to NM_007186.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr2:65296820 A>G maps to NM_015147.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr3:101446273 G>A maps to ENST00000327230 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr16:66974477 G>A maps to NM_003869.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr16:67006755 G>A did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr18:580650 G>T maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr6:31902168 C>A maps to ENST00000418949 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr11:65623201 C>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:47487018 C>A did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr19:49557631 G>T maps to ENST00000377280 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr2:27325299 T>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr3:14157998 G>A maps to NM_144636.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:6202325 G>A maps to NM_015557.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr20:40045242 C>T maps to NM_032221.3 A2157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr14:21861839 T>G maps to NM_001170629.1 P2038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:5905693 G>A maps to NM_001819.2 *678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr16:89720316 A>G maps to NM_002768.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:29535575 G>A maps to NM_004067.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr23:110002886 A>T did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr11:62677197 G>A maps to NM_000738.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr8:27321506 T>G maps to NM_000742.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr15:78893606 A>G maps to NM_000743.4 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr15:78894482 C>T maps to NM_000743.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:233405400 G>A maps to NM_005199.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:45672218 G>A maps to NM_003654.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:101009736 C>A maps to NM_004854.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:125804255 G>A maps to NM_015892.3 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr16:71570879 C>T maps to NM_001166395.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr19:42793430 G>A maps to NM_015125.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr19:42796450 G>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr19:42795389 C>T maps to NM_015125.3 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr19:42796330 C>T maps to NM_015125.3 Q994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:42791827 G>A maps to NM_015125.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:42796878 C>T maps to NM_015125.3 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr16:10997736 C>T maps to NM_000246.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr16:11002909 G>A maps to NM_000246.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:120128189 C>T maps to ENST00000392521 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr1:86919121 C>T maps to NM_006536.5 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:170601231 C>T maps to NM_173872.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr1:16378308 C>T maps to NM_000085.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:16352609 A>G maps to NM_004070.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr1:16377497 G>A maps to NM_000085.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr21:37833826 C>T maps to NM_001146077.1 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:73245692 C>T maps to NM_001305.3 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:3065806 C>T maps to NM_021195.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:7163695 C>T maps to NM_001185022.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr14:38724435 G>A maps to NM_175060.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr14:38724726 G>A maps to NM_175060.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:71043765 G>A maps to NM_173535.2 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr23:154508570 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:139889177 G>A maps to NM_004669.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:25140629 A>G maps to NM_013943.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:56301647 T>C maps to NM_004898.2 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr18:618008 G>A maps to NM_199167.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr8:62371029 C>T maps to NM_173519.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr6:123332252 A>G maps to NM_001010852.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr16:81641213 G>T maps to NM_198390.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:150909278 C>G did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:99006189 C>T maps to NM_001298.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr16:57918280 G>A maps to NM_001297.4 T1181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:21627465 C>A did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr23:21534626 G>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:11660567 C>T maps to NM_001299.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr16:58622798 C>T maps to NM_016284.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr16:58564251 C>A did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr6:88854090 A>G maps to NM_016083.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr17:40956251 A>T maps to NM_173478.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr9:17236519 G>A maps to NM_017738.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr12:41333260 G>A maps to NM_001843.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:147600795 C>T maps to NM_014141.5 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:147259308 C>T maps to NM_014141.5 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr9:39086826 G>C maps to NM_033655.3 Y1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr16:76482069 C>T maps to NM_033401.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:125204402 G>A maps to NM_130773.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:51096965 T>C maps to ENST00000395542 K691K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr7:51097052 C>T maps to ENST00000395542 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr13:46092960 T>C maps to NM_031431.2 N665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:107204266 G>C maps to NM_006348.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr7:107002755 T>C maps to NM_006348.3 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:106851542 C>T did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr8:121290391 A>T maps to NM_021110.1 K1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr9:101832035 G>A maps to NM_001855.3 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr9:101778340 T>C maps to NM_001855.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr10:105793847 A>G maps to NM_000494.3 Y1337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr6:70866053 G>A maps to NM_001858.4 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr17:48270360 G>A maps to NM_000088.3 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr17:48264127 G>A maps to NM_000088.3 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr7:94043556 C>T maps to NM_000089.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr20:61951524 G>A maps to ENST00000326996 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr20:61960982 G>A maps to ENST00000326996 G1321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr6:56044618 G>A maps to NM_030820.3 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr8:139768054 C>T maps to NM_152888.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr8:139793187 G>A maps to NM_152888.1 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr9:116931262 C>T maps to NM_032888.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr2:189867064 C>T maps to NM_000090.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr13:110813711 C>T maps to NM_001845.4 T1489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr13:111147701 C>T maps to NM_001846.2 H1216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr23:107823772 G>T did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:107930899 A>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:107840716 T>C did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr23:107938507 A>T did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:107816842 C>T did not map to a codon.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr23:107821210 A>T did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:107406178 C>T did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr23:107454951 C>T did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr23:107402953 C>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr9:137591839 C>T maps to NM_000093.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr9:137704485 C>T maps to NM_000093.3 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr2:189933562 C>T maps to NM_000393.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr2:189898825 G>A maps to NM_000393.3 G1490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:47423449 C>T maps to NM_001848.2 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr2:238277602 G>A maps to NM_004369.3 D1501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr2:238249143 G>A maps to NM_004369.3 N2805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr2:3691638 C>T maps to ENST00000418971 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr1:160268751 T>C maps to NM_001098398.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr9:100897159 C>T maps to NM_052820.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr20:30231297 T>C maps to NM_032609.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr23:77155050 A>T did not map to a codon.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr3:194062519 G>C maps to NM_001080513.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr16:57147303 C>G maps to NM_152727.5 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:87559940 T>C maps to NM_003909.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr14:24543955 C>T maps to NM_006032.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:211471548 C>T maps to NM_001122633.1 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr2:211525380 T>A did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr11:61183776 A>G maps to NM_024811.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr11:61178543 G>A maps to NM_024811.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr22:51011380 G>C maps to NM_152245.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:50203967 G>A maps to NM_152359.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr7:29134735 C>T maps to NM_031311.3 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr23:88009307 C>G did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:88009268 T>A did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr20:2775985 G>A maps to NM_019609.4 H599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr10:125526578 G>C maps to NM_198148.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:207793264 G>A maps to NM_000651.4 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr1:207890948 G>T maps to NM_175710.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr16:1706071 C>T maps to NM_020825.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:4171093 C>G maps to NM_032607.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr5:76259211 G>A maps to NM_001882.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr7:30695574 G>A maps to ENST00000348438 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr6:49663636 A>G maps to ENST00000211238 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:1321389 G>A did not map to a codon.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr23:1317466 G>T did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr17:29112982 T>C maps to NM_015986.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:99696062 G>A maps to NM_018058.4 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr19:18871030 C>T maps to NM_001098482.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr19:18879356 G>A maps to NM_001098482.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr1:153924629 C>A maps to NM_181715.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr11:45891722 C>T maps to NM_021117.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr22:25623852 C>T maps to NM_000496.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr22:25603097 C>T maps to NM_004076.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr3:97596596 C>T maps to ENST00000182096 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:151908874 G>C did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:1404768 A>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:1409321 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr23:1413342 G>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr17:38172559 C>T maps to NM_000759.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr8:113364707 A>G maps to NM_198123.1 I2064I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr8:113277703 A>G maps to NM_198123.1 N3208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr8:113504736 T>C maps to NM_198123.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr20:18168087 G>A maps to NM_020536.4 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:100077400 A>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:120009415 C>A did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:153881576 C>T did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr20:36431346 C>A maps to NM_030877.3 C370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr23:16608917 A>T did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr11:10783516 C>T maps to NM_014633.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr14:25043507 G>A maps to NM_001911.2 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr4:156847188 C>G maps to NM_001334.2 *322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr10:16883004 C>T maps to NM_001081.3 T3235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr10:16992024 G>A maps to NM_001081.3 G1685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr13:113891148 T>C maps to NM_001008895.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:119669686 C>G did not map to a codon.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr23:119694139 C>G did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr12:111748298 C>A maps to NM_015267.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr12:111729276 C>T maps to NM_015267.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr2:180810176 A>G maps to NM_020943.2 N802N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:36958969 C>T maps to NM_017748.3 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:74863730 G>A maps to NM_002994.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:70837108 G>A did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:30578232 T>C did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:35985794 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:35966454 G>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:35993796 C>A did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:19983582 G>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:19955646 A>C did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:75397597 A>T did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:75396759 C>G did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:149100913 T>A did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:134303694 G>C did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:105855369 G>A did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:23956784 T>C did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:36091354 C>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:37660586 G>C did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:83129575 G>T did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:83116195 T>C did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr15:75012967 G>C maps to NM_000499.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:72359682 G>A maps to NM_019885.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr10:96535296 G>C did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr10:96818193 A>G maps to NM_000770.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:47279203 C>T maps to NM_001099772.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr19:15791262 C>T maps to NM_023944.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr8:59409692 G>A maps to NM_000780.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr17:76694916 C>T maps to NM_004762.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:57756660 G>A maps to ENST00000371231 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr12:109294235 C>T maps to NM_001917.4 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:3964721 C>T maps to NM_001348.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr2:159660848 A>G maps to NM_001017920.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr9:136501813 G>A maps to NM_000787.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:125685929 C>T did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:125686451 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:125299119 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:125298903 C>G did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:125299119 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:125299671 G>A did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:172337524 A>C maps to NM_025000.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr1:167956740 T>C maps to ENST00000367840 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:27999087 G>A did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:27998599 C>A did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:155287389 C>T maps to NM_017639.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:155254332 C>A maps to NM_017639.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr4:155163899 T>C maps to NM_017639.3 K1867K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:155176789 G>A maps to NM_017639.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr4:155287389 C>T maps to NM_017639.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:151153980 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr12:91546925 G>A maps to NM_133503.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr1:155013045 C>T maps to NM_152494.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:74595113 G>A maps to NM_004082.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr19:17425149 C>T maps to NM_024050.5 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr1:15956988 G>A maps to NM_032341.4 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:162746048 C>A maps to NM_006182.2 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:31244795 C>T maps to NM_030653.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:70400562 C>T maps to NM_018332.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:134706885 G>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:134709029 T>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:134711344 A>G did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:134715063 G>A did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:41204457 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:41202024 T>C did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr17:61864441 G>A maps to NM_203499.1 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr12:132624719 C>T maps to NM_175066.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:132626152 T>C did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:686995 G>A maps to NM_021008.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr9:126319962 C>T maps to NM_020946.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr12:100656177 A>C maps to ENST00000422147 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr22:24179852 G>A maps to NM_001135751.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:69421804 G>A did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:69424363 T>A did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr22:19026632 G>A maps to NM_005137.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr3:185997720 G>A maps to NM_001346.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr13:42763201 C>T maps to NM_178009.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:50213437 T>C did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:50127814 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:50147115 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:55337127 G>A maps to NM_014762.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:2161262 T>C did not map to a codon.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr5:54577280 G>C maps to NM_019030.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr20:37634880 C>T maps to NM_021931.3 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:72133710 C>T maps to NM_014003.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr23:96639007 A>T did not map to a codon.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr20:61527923 C>T maps to NM_033081.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr20:61511991 C>T maps to NM_033081.2 P1772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr21:47978200 T>C maps to ENST00000318711 I1289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr21:47952056 G>T maps to ENST00000318711 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:47916994 G>A maps to ENST00000318711 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:12946018 A>C maps to NM_182643.2 P1423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr3:196812551 G>A maps to NM_004087.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr11:83676478 G>A maps to NM_001142699.1 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:69670625 C>T did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:69669654 C>T did not map to a codon.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr18:3879576 G>A maps to NM_004746.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr6:170594118 A>C maps to NM_005618.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr1:46977832 G>A maps to NM_147192.2 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:31747755 G>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr23:32380908 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:32867884 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:32456487 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:31747793 T>C did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr5:78359456 C>A maps to NM_013391.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr19:46275946 G>A maps to NM_004409.3 H432H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr9:1056822 C>T maps to NM_181872.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr9:977180 C>G maps to NM_021240.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr3:52420204 G>A maps to ENST00000273600 R2885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:52380762 C>T maps to ENST00000273600 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:52407043 C>T maps to ENST00000273600 G2320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr12:124332563 C>T maps to NM_207437.3 T1839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr12:124335565 C>T maps to NM_207437.3 P1960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr12:124358199 C>T maps to NM_207437.3 Y2509Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:21721267 C>T maps to NM_003777.3 D1816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr7:21639634 G>A maps to NM_003777.3 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr17:7643863 C>T maps to NM_020877.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:7708391 G>A maps to NM_020877.2 R3100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:7637983 G>A maps to NM_020877.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr16:20990738 C>T maps to NM_017539.1 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr16:21049262 C>T maps to NM_017539.1 S1590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr5:13841809 G>A maps to NM_001369.2 F1825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr5:13736039 C>G maps to NM_001369.2 V3819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr5:13751312 G>T maps to NM_001369.2 T3695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr5:13919349 A>G maps to NM_001369.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr2:84784901 T>G maps to NM_001370.1 L549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:38980112 G>A maps to ENST00000327475 L4486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr6:38893889 T>A maps to ENST00000327475 I3662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:11671915 C>T maps to NM_001372.3 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:11660880 G>A maps to NM_001372.3 P2289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr2:234652337 G>A maps to NM_001001394.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:234652391 C>T maps to NM_001001394.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr22:41257197 C>T maps to NM_145174.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr2:183593667 C>T maps to NM_018981.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:6697341 G>A maps to NM_018198.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr1:65858363 T>G maps to ENST00000371069 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr17:40133942 G>A maps to NM_003315.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr2:25457208 C>T maps to NM_175629.1 W893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:31368260 G>A maps to NM_006892.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:117773443 T>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr23:117695459 G>A did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr8:25216577 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-FG-A60K-01A-11D-A29Q-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:11347157 G>A maps to ENST00000319867 N752N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr1:62995073 A>G maps to ENST00000371140 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr9:289508 G>A did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr21:35288046 G>A maps to NM_001697.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr6:83839855 C>T maps to NM_015018.2 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:68026418 G>A maps to NM_022355.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr17:1936712 G>A maps to ENST00000417873 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr2:116497432 G>A maps to NM_020868.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr12:7867928 G>A maps to NM_199286.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr12:7867803 G>A maps to NM_199286.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr7:34978934 T>A maps to NM_015283.1 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr12:63994084 C>T did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr8:105459568 C>A maps to NM_001385.2 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr8:26484190 C>T maps to NM_001197293.1 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:100490938 G>A did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr18:28725702 G>A maps to NM_024421.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr11:117308780 G>T maps to NM_020693.2 S1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr18:28934738 A>G maps to NM_001942.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr18:28923926 C>T maps to NM_001942.2 N620N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr18:29102121 C>T maps to NM_001943.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr18:29099848 C>T maps to NM_001943.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr18:29126612 T>C maps to NM_001943.3 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr18:28993041 T>A maps to NM_001134453.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:7571617 G>A maps to NM_004415.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr6:7583353 C>A maps to NM_004415.2 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr4:88534156 T>C maps to NM_014208.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:205138720 G>A maps to NM_015375.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr15:45401121 G>A maps to NM_014080.4 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr15:45389889 G>A maps to NM_014080.4 F1205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr10:76803651 G>A maps to NM_001003892.1 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr10:76803656 G>A maps to NM_001003892.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr6:348773 G>T maps to ENST00000457386 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr6:348271 C>T maps to ENST00000457386 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr1:167096395 G>A maps to NM_001080426.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:1578530 C>T maps to NM_004420.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr17:7132712 T>C maps to NM_004422.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:33122559 C>T maps to ENST00000374846 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr15:55731773 T>C maps to NM_130810.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr5:158140056 G>A maps to NM_024007.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:158158157 G>A maps to NM_024007.3 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr23:68836452 C>T did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr2:109547446 C>T maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:184695448 T>C maps to NM_025191.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr4:148407183 G>T maps to NM_001957.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr19:3977233 G>A maps to NM_001961.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr8:49643960 G>A maps to NM_024593.3 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:28409943 C>T maps to NM_198529.3 Y1154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:44120531 C>T did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr13:107147325 T>A maps to NM_004093.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr5:38338819 C>T maps to ENST00000354891 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr7:55260472 G>A maps to NM_005228.3 W880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:137803724 G>A maps to NM_001964.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:63182657 T>C maps to NM_015252.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:31848859 C>T maps to ENST00000395728 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr23:20156712 C>A did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:20156718 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:20156712 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:20156728 T>C did not map to a codon.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr15:40258022 G>A maps to NM_001013703.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr12:124111688 G>A maps to NM_001414.3 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:141595387 C>T maps to NM_012154.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:120796751 G>A maps to NM_003750.2 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr1:32688224 G>A maps to NM_003757.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr22:38270461 C>T maps to ENST00000262832 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:21268143 G>A maps to NM_001198801.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr14:103802434 G>A maps to NM_183004.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr19:852924 C>T maps to NM_001972.2 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr9:23701563 G>A maps to ENST00000359598 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:37770332 G>A maps to NM_052906.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr19:18557616 G>A maps to NM_006532.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:85617290 C>T maps to NM_001135023.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr18:33738839 G>T maps to ENST00000442325 G568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:79392753 T>A maps to NM_022159.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr1:79470842 G>C maps to NM_022159.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:79470884 C>T maps to NM_022159.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr12:7083746 C>T maps to ENST00000261406 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr14:89160702 A>T maps to ENST00000380664 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr19:6937658 G>A maps to ENST00000381407 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:71510352 C>T maps to NM_031889.2 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:130587088 G>A maps to NM_001114753.1 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:111397843 C>T maps to NM_001977.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr8:120596282 A>G maps to NM_006209.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr6:46129356 G>A maps to NM_021572.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:150599963 G>A maps to NM_207042.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr10:101464241 T>C maps to NM_020354.3 H539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr22:41566475 T>C maps to NM_001429.3 H1451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr12:132466656 G>T maps to ENST00000333577 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr12:132466833 G>A maps to ENST00000333577 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr12:132547107 G>A maps to ENST00000333577 Q2768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:34770233 G>A maps to NM_012156.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr6:131188676 T>C maps to NM_001431.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr2:149528636 A>G maps to NM_015630.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:89448614 G>T maps to NM_005233.5 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr1:22924292 G>A maps to NM_020526.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr7:100421496 C>A maps to NM_004444.4 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr7:142564302 G>A maps to NM_004445.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr7:142562151 G>A maps to NM_004445.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr7:142568142 C>T maps to NM_004445.3 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:142561053 G>T maps to NM_004445.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:48616600 C>T maps to NM_017957.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr8:144942252 G>A maps to NM_031308.1 D1723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr8:144942234 G>A maps to NM_031308.1 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr8:144940575 C>T maps to NM_031308.1 S2282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr8:144942912 G>A maps to NM_031308.1 S1503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr1:220142261 T>A maps to NM_004446.2 G1475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr19:16487939 C>T maps to ENST00000455140 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr19:55597451 G>A maps to NM_133180.2 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:56026257 G>A maps to ENST00000460849 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:45916940 A>T maps to NM_202001.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr21:39755663 G>A maps to NM_001136154.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:62144065 C>T maps to NM_001433.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr12:53680350 A>G maps to NM_012291.4 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr1:6488428 C>T maps to NM_031475.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr14:76905887 C>T maps to NM_004452.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:103499229 C>A did not map to a codon.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr4:159603572 G>A maps to NM_004453.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr17:74003588 G>T maps to NM_001988.2 A1899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr22:29694856 C>T maps to NM_013986.3 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:56734653 G>T maps to NM_018261.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8019-01A-21D-2395-08 chr10:94700481 A>T did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr17:74084887 G>T maps to NM_001145297.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr11:108381247 G>A maps to NM_015065.2 N1662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:26349415 C>T maps to NM_004455.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr1:26360305 C>T maps to NM_004455.2 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr6:133783470 A>T did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr17:40869992 C>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr6:159188409 G>A maps to NM_001111077.1 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr1:169519049 G>A maps to ENST00000367796 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:154194744 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:154065951 G>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:154159215 T>C did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr23:57358191 C>T did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr4:120243251 C>T maps to NM_000134.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr2:96071500 G>A maps to NM_016044.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr3:138341216 G>A maps to NM_001033030.1 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr11:126126562 C>G maps to NM_024556.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr9:96326728 C>T maps to ENST00000333936 C1116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr9:96324504 T>A maps to ENST00000333936 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:54209050 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr13:25743873 T>C maps to NM_152704.2 Q628Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr23:63411384 G>A did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:63411821 C>T did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:63410719 C>T did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr23:63412956 A>G did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:63412446 A>G did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr2:131521708 C>T maps to NM_001105195.1 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr2:131521799 C>T maps to NM_001105195.1 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr13:51825994 C>T maps to NM_145019.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr2:225266431 A>G maps to NM_001122779.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr1:184863334 T>C maps to NM_052966.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr5:16475173 C>T maps to NM_001034850.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr5:175533579 C>A maps to NM_001079529.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr2:29222092 G>A maps to NM_199280.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr16:57206706 G>A maps to NM_024946.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr4:2696819 C>T maps to ENST00000324666 C789C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:103411603 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr21:42710401 C>T maps to ENST00000398652 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr3:194408802 T>C maps to NM_153690.4 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:118166434 C>T maps to NM_017709.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:34150159 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:34148779 C>T did not map to a codon.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr23:34149059 C>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:34149531 G>A did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:34961314 G>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:34962024 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:34961869 C>T did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:34962575 G>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:34962763 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:34961354 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:37027823 G>T did not map to a codon.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:37027910 G>A did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:37027100 G>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:24380908 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:24380950 G>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr23:24381604 C>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:24330362 G>C did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:153678569 A>C did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:152853847 T>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr16:67578713 G>A maps to NM_001193523.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr6:24843452 G>A maps to NM_014722.2 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr20:49225173 C>T maps to NM_080829.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr20:49224996 C>T maps to NM_080829.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:119410864 C>T did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:156589801 G>A maps to NM_130899.2 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:156590150 C>T maps to NM_130899.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr5:156593085 A>G maps to NM_130899.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr12:100043169 G>A maps to NM_153364.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr9:43625419 A>G maps to NM_001145196.1 C1089C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr9:90536582 C>T maps to NM_001145124.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr9:90535985 G>A maps to NM_001145124.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:90535985 G>A maps to NM_001145124.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr9:134136481 C>T maps to NM_033387.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr5:94749821 C>T maps to NM_152548.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr6:54735128 C>T maps to NM_001010872.1 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr17:18874944 G>A maps to NM_001039999.2 N733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr1:231155647 G>A maps to NM_198552.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr12:8376781 G>A maps to NM_018088.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:8993590 C>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:14883270 C>T did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr23:14863148 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr3:10123118 G>A maps to NM_033084.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr14:45623199 A>G maps to NM_020937.2 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr13:99076870 C>T maps to NM_005766.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:5431388 A>G maps to NM_006567.3 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr1:172634804 C>A maps to NM_000639.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:172628550 C>A maps to NM_000639.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr17:80051591 G>A maps to NM_004104.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr4:187524636 A>G maps to ENST00000260147 V3684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr5:150922416 G>A maps to NM_001447.2 H2757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:150943009 A>G maps to NM_001447.2 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:150924338 G>A maps to NM_001447.2 R2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr11:92600242 C>T maps to ENST00000298047 Q3999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:126239158 C>T maps to NM_024582.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:126239281 C>G maps to NM_024582.4 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:45914667 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr3:13655524 C>T maps to NM_001165035.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr2:112944824 C>T maps to NM_153214.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr15:48795984 T>C maps to NM_000138.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr15:48729543 G>T maps to NM_000138.4 I2118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr15:48764790 G>A maps to NM_000138.4 C1431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr19:8152977 G>A maps to NM_032447.3 D2154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:8188414 C>T maps to NM_032447.3 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr8:145580131 G>A maps to NM_012162.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr5:15937210 C>T maps to NM_012304.3 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr7:100187921 G>A maps to NM_012172.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr6:146126347 A>G maps to NM_032145.4 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr14:39870638 G>A maps to NM_203301.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr8:101146457 T>C maps to NM_001029860.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr19:46216179 G>A maps to NM_001080469.1 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr12:117448195 G>A maps to NM_153348.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr19:40357727 G>A maps to NM_003890.2 S5195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr19:17895688 G>A maps to NM_015122.2 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr9:137804959 G>T maps to NM_002003.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr1:157766908 C>T maps to NM_052938.4 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr1:157667653 C>A maps to NM_052939.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr1:157665875 G>A maps to NM_052939.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr1:157490930 C>T maps to NM_031281.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:161681130 C>T maps to NM_001184866.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr8:125082818 C>T maps to NM_001039112.2 R1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr15:91437241 C>T maps to NM_002005.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr19:35862413 C>T maps to ENST00000246538 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr19:35850685 G>A maps to NM_005304.3 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr6:36978765 C>T maps to NM_173558.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr9:95795122 C>T maps to NM_033086.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:95738978 C>T maps to NM_033086.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr12:32791722 C>G maps to NM_139241.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr3:14862335 G>A maps to NM_152536.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr3:14862572 G>A maps to NM_152536.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr12:95604906 T>G maps to NM_018351.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr13:103053947 C>T maps to NM_175929.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr8:16850595 T>C maps to NM_019851.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:49261317 A>C maps to NM_019113.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr12:4479523 G>A maps to NM_020638.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr11:69631174 C>T maps to NM_005247.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr5:176519744 C>T maps to NM_213647.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr5:176520244 G>A maps to NM_213647.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr7:76826041 G>A maps to NM_006682.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:27943401 G>A maps to NM_005248.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:133780651 C>T maps to NM_001145106.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:15365419 A>G did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr7:50513533 T>C maps to NM_022116.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:76024623 C>T maps to NM_015687.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr12:2910515 G>A maps to NM_002014.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:72754698 C>T maps to NM_003602.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr19:18650227 C>T maps to NM_012181.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:152275718 C>T maps to NM_002016.1 E3881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:152280317 G>A maps to NM_002016.1 H2348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr1:152282000 T>C maps to NM_002016.1 G1787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr1:152281298 G>A maps to NM_002016.1 G2021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr23:153595806 G>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:153588483 C>T did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:153593775 A>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr3:58111407 C>T maps to NM_001164317.1 A1333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr3:58095049 G>C did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr3:58080623 C>T maps to NM_001164317.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:58108830 C>T maps to NM_001164317.1 H1046H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr3:58097874 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr7:128482971 G>A maps to NM_001458.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:128488740 G>A maps to NM_001458.4 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:128489529 C>T maps to NM_001458.4 D1699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr7:128480692 G>A maps to NM_001458.4 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr14:86089273 C>T maps to NM_013231.4 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr20:14307456 C>T maps to NM_198391.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr13:28611412 A>G maps to NM_004119.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr13:28609683 A>G maps to NM_004119.2 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr5:180043381 G>A maps to NM_182925.4 Y1068Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:180046722 G>A maps to NM_182925.4 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr14:76101272 A>G maps to NM_017791.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr16:2983272 G>A maps to ENST00000399667 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:240371420 C>T maps to ENST00000406993 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:43314942 G>T maps to NM_005892.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr2:153473699 C>T maps to NM_052905.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr12:50043068 A>G maps to NM_175736.4 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:171079964 C>G maps to NM_006894.5 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:171300884 A>G maps to NM_002022.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:203316987 G>A maps to NM_002023.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:203311548 G>A maps to NM_002023.3 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:147010282 T>C did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr23:147106437 A>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:147084822 A>G did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr11:47753112 C>T maps to NM_015308.2 R607R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CS-4941-01A-01D-1468-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr13:49772708 C>A maps to ENST00000497644 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr11:49207239 T>C maps to NM_004476.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:70177704 C>T maps to NM_001126334.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr16:86546528 A>G did not map to a codon.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr14:29237033 G>A maps to NM_005249.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:8200511 G>A maps to NM_018416.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr17:80544071 C>G maps to NM_004514.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr12:2968214 C>T maps to NM_202002.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr7:114269948 A>G maps to NM_148898.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr23:55650389 G>A did not map to a codon.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr20:30432673 G>A maps to NM_004118.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr9:130570868 C>G maps to NM_004957.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EY-01A-11D-A27K-08 chr19:52327321 C>A maps to NM_002030.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr4:79204002 C>A maps to NM_025074.6 C379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr4:79387411 C>T maps to NM_025074.6 I2360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr10:13825005 C>T maps to NM_018027.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr10:13698930 G>A maps to NM_018027.3 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:131216496 A>G did not map to a codon.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr23:131214291 C>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:131212490 A>G did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr23:131214036 T>C did not map to a codon.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr23:12701667 C>T did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr23:12736403 C>T did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:12735804 C>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:12720060 C>T did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:12736147 T>C did not map to a codon.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr23:12734263 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:12736537 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr6:41738832 G>A maps to NM_006653.3 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr13:32747574 A>C maps to NM_023037.2 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr13:32852685 G>C did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:48536662 G>A maps to NM_015030.1 L2202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr14:44975037 G>T maps to NM_032135.3 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr19:4310576 A>G maps to NM_024333.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr15:39910062 C>T maps to NM_152597.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr19:681420 G>A maps to NM_005860.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr4:162463804 T>C maps to NM_020116.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr4:162577527 C>T maps to NM_020116.3 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr4:162697148 G>A maps to NM_020116.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr5:121187708 G>A maps to NM_177478.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr5:121188110 C>T maps to NM_177478.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr23:48337055 A>G did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:48339828 G>T did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr1:78430844 C>A maps to ENST00000436586 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr1:78422351 C>T maps to ENST00000436586 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:78432435 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr1:78429936 A>C did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr1:78430552 A>G did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr1:78429847 C>T did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr1:78435639 A>C maps to ENST00000436586 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr1:78435642 A>C maps to ENST00000436586 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:78430772 C>A maps to ENST00000436586 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr1:78420961 C>T maps to ENST00000436586 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr1:78429791 A>T maps to ENST00000436586 C353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr6:143823181 T>C maps to NM_032020.4 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr11:94278273 C>T maps to NM_002033.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr5:39202452 G>A maps to ENST00000263405 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr5:39203056 C>T maps to ENST00000263405 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:46014620 C>T maps to NM_024513.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr3:46023169 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr8:104337522 C>T maps to NM_003506.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr1:209849304 C>T maps to NM_015714.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:153761825 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:153760889 G>A did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:153762633 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:153906496 G>C did not map to a codon.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr22:17444665 C>G maps to NM_001037814.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:151336929 A>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:151532993 G>C did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:151336861 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr5:161119013 A>T maps to NM_000811.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr15:27184435 G>A did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:151123360 C>T did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:151123278 C>T did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:46060561 A>G maps to NM_173536.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr5:161580181 C>T maps to NM_198903.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr3:30885752 A>G maps to NM_207359.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr1:24124672 G>A maps to NM_001008216.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr2:38903111 C>T maps to NM_138801.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:11470397 G>T maps to NM_198516.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr11:62400105 G>A maps to NM_198335.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr9:128124937 T>C maps to NM_015635.2 A1459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr21:34911629 C>T did not map to a codon.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr13:114531663 C>T maps to ENST00000357389 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:48650341 C>T did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr10:8100436 G>A maps to NM_001002295.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr10:8100385 G>A maps to NM_001002295.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr12:120894950 C>T maps to NM_176818.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:45658330 T>C maps to ENST00000432007 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr9:35741040 T>C maps to NM_020944.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:104141972 C>T maps to NM_004193.2 G1820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr1:89520409 G>C maps to NM_002053.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr1:89730623 A>G maps to NM_052942.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr19:13006896 A>G maps to NM_000159.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr9:79117863 G>A maps to NM_001097636.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr6:10529179 G>A maps to NM_145649.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr15:59911327 G>A maps to NM_004751.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr15:57976626 G>C maps to NM_001018100.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr1:118441727 C>A maps to NM_017686.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr12:7843232 G>A maps to NM_020634.1 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:97156958 G>A maps to NM_001001557.2 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:153668415 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:153670770 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:69652186 C>A did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:69652494 A>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:69652259 G>A did not map to a codon.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr8:21608323 C>T maps to NM_001495.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:30538451 G>A maps to NM_024051.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:38876365 G>A maps to NM_152657.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:4461801 G>A maps to ENST00000414312 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr20:33439057 C>T maps to NM_178026.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr11:59611460 T>C maps to NM_005142.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr7:100280313 G>A maps to NM_022574.4 G833G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr2:233674459 C>T maps to ENST00000373566 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr19:14591416 G>A maps to NM_202470.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr13:20763147 G>A maps to NM_004004.5 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr17:42882003 G>A maps to NM_001080383.1 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:30739085 G>A did not map to a codon.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr4:80327818 A>G maps to NM_033214.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr11:134147258 C>T maps to NM_001080407.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr2:121684943 G>A maps to NM_005270.4 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr7:42006177 G>A maps to NM_000168.5 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:53995559 C>T maps to NM_147193.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr16:4383345 A>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr9:3828286 G>C maps to NM_001042413.1 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:685480 T>C maps to NM_016080.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr19:17690295 G>A maps to NM_024656.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr1:183938502 C>T maps to NM_015101.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr9:138516116 C>T maps to NM_182974.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:120181765 C>T did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:120182835 G>A did not map to a codon.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr2:70092030 G>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr6:1961059 C>T maps to NM_001500.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:19745857 T>G maps to NM_016573.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr18:11880998 G>A maps to NM_182978.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr16:56388961 C>G maps to NM_020988.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr9:36249250 G>A maps to NM_001128227.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr3:52727061 G>A maps to NM_014366.4 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr4:68606312 C>T maps to NM_000406.2 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr9:131022429 C>T maps to NM_004486.4 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr3:37396654 G>T maps to NM_001172713.1 E2229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr19:33608852 A>G maps to NM_018025.2 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr1:27224100 C>T maps to NM_022078.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr5:56546840 C>T maps to NM_001127236.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr1:46120874 T>C maps to NM_021639.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:46120390 G>A maps to NM_021639.4 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:132887605 C>A did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:132887715 G>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:133087086 C>T did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:132458382 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:132548971 C>T did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr14:67576891 G>A maps to NM_020806.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:48972593 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:13795536 A>G did not map to a codon.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr6:46976956 G>C maps to ENST00000283297 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:135405391 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:135405490 G>A did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:135405537 G>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:135430979 G>C did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:135428468 G>C did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr23:135432486 G>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:135429889 C>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:47680158 C>T maps to NM_153838.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr6:46826759 C>T maps to NM_015234.4 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr10:134898494 T>C maps to ENST00000368577 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr8:37698690 C>T maps to NM_032777.9 C945C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:236341828 C>T maps to NM_003272.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr16:20043245 C>G maps to NM_001002911.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr12:6933474 C>T maps to NM_019858.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:78427487 G>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr13:95275436 G>C maps to NM_180989.4 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr13:95273350 A>G maps to NM_180989.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:125426408 G>A maps to NM_153442.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr3:71803790 G>T maps to NM_018971.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr6:167570605 G>A maps to NM_005299.2 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:51274117 C>T maps to NM_001506.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:41555136 G>A did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:133175295 C>T maps to NM_001508.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr2:105858977 G>A maps to NM_007227.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:150349209 C>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:150349611 C>A did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr2:231774732 C>T maps to NM_005683.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr6:110301178 C>T maps to ENST00000414000 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr6:97246404 C>T maps to NM_030784.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:19027858 A>T did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:19031905 G>A did not map to a codon.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr14:91700785 C>T maps to ENST00000238699 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr5:89933729 G>A maps to NM_032119.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr5:90119412 G>A maps to NM_032119.3 K5456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr5:89979458 T>C maps to NM_032119.3 S1907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:101909473 A>G did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:101912053 G>A did not map to a codon.
Sequencing variant TCGA-FG-6691-01A-11D-1893-08 chr23:101909850 G>C did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr16:19883180 G>C maps to NM_016235.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr16:19883825 G>T maps to NM_016235.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr17:72436709 C>T maps to NM_022036.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr5:176026757 G>A maps to NM_052899.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:176025904 C>A maps to NM_052899.2 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr14:65406295 C>T maps to NM_002083.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:28472104 G>A maps to NM_182701.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:35504507 C>T maps to NM_020895.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr3:113563351 G>T maps to NM_017577.4 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr17:18927575 G>A maps to NM_006613.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr7:50686968 T>C maps to NM_005311.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:240656343 G>A maps to NM_022469.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:24671384 A>C did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:122561826 G>A did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:122616847 T>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:122598964 T>A did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:122538739 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr16:10274070 G>A maps to NM_000833.3 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr12:13764767 G>A maps to NM_000834.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr12:13716186 G>A maps to NM_000834.3 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:13716622 C>T maps to NM_000834.3 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr9:104499940 C>T maps to NM_133445.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:1004801 C>T maps to NM_138690.1 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:48831680 C>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:48830665 C>T did not map to a codon.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr5:176857876 C>T maps to NM_002082.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr6:146720658 G>C maps to NM_000838.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr7:86468866 G>A maps to NM_000840.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr5:178418950 C>T maps to NM_000843.3 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr3:7620371 T>C maps to NM_181874.2 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:16168587 A>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:16142350 C>T did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr23:16170453 C>A did not map to a codon.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr17:38073446 C>T maps to NM_001165958.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr8:144645067 C>A maps to NM_024736.6 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr3:119720904 G>A maps to NM_002093.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:51488254 T>A did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:51488447 G>A did not map to a codon.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr6:52767169 G>A maps to NM_000847.4 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:74212377 T>C maps to NM_173537.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr2:197657736 C>T maps to NM_012086.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr9:135546107 G>T maps to NM_012204.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr6:42162501 C>T maps to NM_002098.5 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:108719024 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr23:108718946 C>A did not map to a codon.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr4:44693680 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr12:42512816 A>G maps to NM_173601.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:2799185 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:54329738 G>A maps to NM_002104.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:103267992 G>T did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr2:26437419 C>T maps to NM_000182.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:26414364 C>T maps to NM_000182.4 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr5:82937338 G>A maps to NM_001884.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr19:52220446 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr18:43700023 A>G maps to NM_138443.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr9:19093263 G>C maps to NM_017645.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr16:202925 T>C maps to NM_005332.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:11133052 C>A did not map to a codon.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr23:11135491 T>C did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:153225449 G>C did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:153228836 A>C did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr20:30667666 C>T maps to NM_002110.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr20:30659554 C>T maps to NM_002110.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr5:45262042 G>A maps to NM_021072.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr5:45262355 G>T maps to NM_021072.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr1:155257755 G>A maps to NM_020897.1 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr15:73615169 C>T maps to NM_005477.2 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr2:239976490 G>A maps to NM_006037.3 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:48682451 A>G did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:48682403 G>T did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:242176035 A>C maps to NM_005336.3 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:83724442 A>C did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:83616610 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:83723853 A>G did not map to a codon.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr23:83724059 G>T did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:236724538 T>C maps to NM_018072.5 K1544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:236738050 C>T maps to NM_018072.5 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr14:73989792 G>A did not map to a codon.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr2:37289162 G>A maps to NM_019024.1 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr17:58133571 G>A maps to NM_022070.4 Y702Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr5:41055886 T>A maps to ENST00000296803 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr5:41004890 G>A maps to ENST00000296803 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr5:41058281 G>A maps to ENST00000296803 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr5:41070935 C>A maps to ENST00000296803 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr6:139487913 G>T maps to NM_016217.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr14:31576336 G>A maps to NM_015382.2 F2247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr7:43483865 G>A maps to NM_015052.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:43581597 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:43484732 C>T maps to NM_015052.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:96352240 G>A maps to NM_018063.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr17:65105676 A>G maps to NM_014877.3 A1348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:65427078 T>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:65427137 G>A did not map to a codon.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr15:63972936 C>T maps to ENST00000261887 T2088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr7:35707096 T>C maps to NM_022373.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr15:72668151 C>T maps to ENST00000457859 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr1:91818119 A>G maps to NM_001017975.3 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr3:120360507 G>A maps to NM_000187.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:81339499 G>A maps to NM_000601.4 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr17:79653395 C>T maps to NM_004712.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr1:210761337 C>T maps to NM_001170580.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr4:145579960 G>A maps to NM_022475.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr1:222717480 C>T maps to NM_024746.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr19:40895407 G>A maps to NM_144685.3 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr6:26056629 G>C maps to NM_005319.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:26225732 C>T maps to NM_003532.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:143095692 T>C maps to NM_006734.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr1:42048875 G>A maps to NM_024503.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr1:42049198 G>A maps to NM_024503.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr1:42050150 C>T maps to NM_024503.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr10:71160765 C>T maps to ENST00000439900 Q912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:75107688 C>T maps to NM_000189.4 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr6:32975238 G>C maps to NM_002119.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr6:32975226 C>T maps to NM_002119.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr6:32975790 G>A maps to NM_002119.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr6:32974942 A>G maps to NM_002119.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr6:33052886 C>A maps to NM_002121.4 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:29693048 C>T maps to NM_001098479.1 H284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr6:29855968 T>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr6:29855998 G>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr3:148792095 A>C maps to NM_003071.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr1:186045566 A>T maps to NM_031935.2 P2766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr1:186055384 A>T maps to NM_031935.2 P2964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr1:185969240 C>T maps to NM_031935.2 G1313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr1:186084408 G>A maps to NM_031935.2 P3808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr1:186056427 C>T maps to NM_031935.2 G3042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr12:66221788 C>T maps to NM_003483.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr17:36059195 G>A maps to NM_000458.2 Y513Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:179043154 G>A maps to NM_005520.2 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:100667034 G>T did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:27224589 G>A maps to NM_005523.5 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr7:27169088 G>A maps to NM_002141.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr7:27187207 G>T maps to NM_024014.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:46669798 C>G maps to NM_002147.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr12:54338832 G>A maps to NM_017410.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr2:177034189 A>G maps to NM_006898.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr16:72110679 C>T maps to ENST00000228226 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr16:72110613 A>G maps to ENST00000228226 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr3:148884978 G>A maps to NM_032383.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr8:21982884 C>T maps to NM_005144.4 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:49656970 G>A maps to NM_002152.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr3:186383867 G>A maps to NM_000412.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr20:60793681 G>A maps to ENST00000317393 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr1:152187066 A>T maps to NM_001009931.1 S2346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr1:152192865 G>A maps to NM_001009931.1 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr1:152193267 C>T maps to NM_001009931.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr16:26147049 T>A maps to NM_006040.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr16:1962139 C>T maps to ENST00000454677 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:132091352 C>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:131762857 T>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr17:40705301 C>T maps to NM_000413.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:82104637 C>T maps to NM_002153.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr5:118867013 G>A maps to NM_000414.3 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr21:15748039 G>A maps to NM_006948.4 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr9:128001228 C>T maps to NM_005347.4 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr5:137906679 G>A maps to NM_004134.6 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr5:53751846 C>T maps to NM_006308.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr2:198352635 A>T maps to NM_199440.1 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr1:22211317 G>A maps to NM_005529.5 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:22159013 G>A maps to NM_005529.5 G3727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr1:22174481 G>A maps to NM_005529.5 I2614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:22166339 C>T maps to NM_005529.5 T3228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:23519884 G>A maps to NM_000864.4 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr6:87725426 C>A maps to NM_000865.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr2:231973907 G>A maps to NM_000867.4 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:113803067 C>A maps to NM_006028.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr3:183774717 C>T maps to NM_130770.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr5:147889455 G>T maps to NM_001040173.2 Y213*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:154862917 C>T maps to NM_024012.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr4:3225847 G>A maps to NM_002111.6 P2585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:53654433 C>T did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:53618081 G>C did not map to a codon.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr12:111099097 G>C maps to NM_001040107.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr3:50332973 G>A maps to NM_003549.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr19:10445306 A>G maps to NM_002162.3 N363N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:45651220 G>A maps to ENST00000400379 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr10:94266255 C>T maps to NM_004969.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:148568541 C>T did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr6:30711943 C>T maps to NM_003897.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr11:314977 C>T maps to ENST00000328221 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr11:298551 C>T maps to NM_001025295.1 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:21201903 G>A maps to NM_021057.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr21:34717550 G>C did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr21:34625022 G>A maps to NM_207585.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:50326251 G>A maps to ENST00000336089 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr15:65684523 C>T maps to NM_020962.1 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr3:185393094 G>A maps to NM_006548.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr4:71527852 G>A maps to NM_144646.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr23:130416638 C>G did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:130413284 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:130415781 T>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr3:151163026 G>T maps to NM_178822.4 S1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr11:18739487 G>A maps to NM_173588.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr7:50459520 C>T maps to NM_006060.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:37947816 A>G maps to NM_012481.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr11:117869740 G>T maps to NM_001558.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr19:18191675 C>T maps to NM_005535.1 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr19:18183117 C>T maps to NM_005535.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr23:117900528 A>G did not map to a codon.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr15:81571958 C>T maps to NM_172217.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr22:50435798 G>A maps to NM_001001694.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr2:102984510 T>A maps to NM_003855.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:103013336 C>T maps to NM_003855.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:113591146 G>A maps to NM_000576.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:29972756 G>T did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:105011343 T>G did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:104984621 A>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:104999269 T>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:102957202 C>T maps to NM_016232.4 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr2:102968089 C>T maps to NM_016232.4 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr2:102835530 A>G maps to NM_003854.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:207039238 G>A maps to NM_018724.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr16:27448928 C>T maps to NM_181079.4 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:27445713 G>A maps to NM_181079.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr1:24447957 G>A maps to NM_021258.2 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:24463672 C>T maps to NM_021258.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr16:28510980 G>A maps to NM_145659.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr19:14157293 G>A maps to NM_004843.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr19:14157388 G>A maps to NM_004843.2 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr19:39788647 G>A maps to NM_172140.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr10:6061421 C>T maps to NM_000417.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr12:122658747 G>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:50393076 C>T maps to NM_172374.1 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr16:27372136 G>A did not map to a codon.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:135231430 C>T maps to NM_000590.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:155239556 C>T did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:155234152 A>G did not map to a codon.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr7:128040206 C>T maps to NM_000883.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:61912745 C>T maps to NM_001040694.1 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr7:120590816 T>C did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr7:120590816 T>C did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr7:120590816 T>C did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr7:120590816 T>C did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr2:74684816 G>A maps to ENST00000452361 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:143094940 G>A maps to NM_003866.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr10:134521842 C>A maps to NM_005539.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr10:121551478 C>G maps to NM_014937.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:31522442 C>T maps to ENST00000331075 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr1:156823628 C>T maps to NM_014215.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:1538969 C>A maps to ENST00000389470 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr11:77672046 G>A maps to NM_033547.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr11:77639507 A>T maps to NM_033547.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr14:24651579 G>A maps to ENST00000458132 H834H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr1:201817720 A>G maps to NM_018085.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr2:237272425 G>A maps to ENST00000457693 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr3:51929061 G>A maps to NM_152397.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:67629359 G>A maps to NM_001031715.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr15:91034588 C>T maps to NM_003870.3 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr1:156499980 G>C maps to NM_178229.4 V1440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr12:274928 C>T maps to NM_001170738.1 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr6:407543 C>T maps to NM_002460.3 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr16:85952326 C>T maps to NM_002163.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr16:85952179 G>A maps to NM_002163.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:44222961 G>A maps to NM_019612.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr2:227662185 G>A maps to NM_005544.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:227660232 C>T maps to NM_005544.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:107978514 G>T did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:107978401 G>A did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:107979042 C>G did not map to a codon.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr5:2749841 G>A maps to NM_033267.4 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:55362678 G>A maps to NM_024335.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:55361632 C>G maps to NM_024335.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr20:33068912 C>T maps to ENST00000262650 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:145534933 C>T maps to NM_003637.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:48157735 C>T maps to NM_002204.2 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:56094109 G>A maps to ENST00000347027 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr16:31419094 C>T maps to ENST00000444228 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr17:3656700 C>T maps to NM_002208.4 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr16:30530024 C>T maps to NM_002209.2 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr16:31308839 C>T maps to NM_001145808.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr16:31391361 G>A maps to NM_000887.3 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:70524874 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr21:46320363 C>T maps to NM_000211.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr17:73736511 C>T maps to NM_001005619.1 C840C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr2:160982990 G>A maps to NM_000888.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr3:52812972 C>T maps to NM_002215.2 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr3:52824843 C>T maps to NM_002215.2 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr10:7780698 G>A maps to NM_002216.2 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr3:52848084 G>A maps to ENST00000485816 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr10:7679257 C>T maps to ENST00000256861 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr1:160850420 G>A maps to NM_017625.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr19:41223411 A>C maps to NM_025194.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr3:4819012 C>A maps to ENST00000356617 I2078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:33626883 C>T maps to ENST00000374316 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr21:35183493 G>A maps to NM_003024.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr21:35183493 G>A maps to NM_003024.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr20:10622191 C>T maps to NM_000214.2 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr20:10624438 G>A maps to NM_000214.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:105615618 G>A maps to NM_002226.3 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr1:65303661 A>G maps to NM_002227.2 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:65323386 G>A maps to NM_002227.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr9:5090495 C>T maps to NM_004972.3 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr4:6043921 G>A maps to NM_001099433.1 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr10:133967331 G>T did not map to a codon.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr11:134018706 C>T maps to NM_032801.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr14:59970666 G>A maps to ENST00000356057 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr16:87678020 C>T maps to NM_020655.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr16:87678404 G>A maps to NM_020655.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr14:24040637 G>A maps to NM_032452.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:8555922 T>C did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:8503843 G>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr3:124393413 G>A maps to NM_001024660.3 A2382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr9:713192 G>A maps to NM_015158.2 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:5021389 C>T maps to NM_000217.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr3:155838414 G>T maps to NM_172160.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr8:73480217 C>T maps to NM_004770.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:48826089 C>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:119914853 G>A maps to NM_012281.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr20:49626812 G>A maps to NM_002237.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr18:77624218 G>A maps to NM_012283.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr18:77659302 C>G maps to NM_012283.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr12:49937974 G>T maps to NM_012284.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr3:19575086 C>T maps to NM_144633.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr3:19575086 C>T maps to NM_144633.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:88652406 G>A maps to NM_138318.2 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr14:90650848 G>A maps to NM_022054.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr10:118957047 C>T maps to NM_181840.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:154842347 C>T maps to NM_002249.4 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr2:18113039 G>A maps to NM_002252.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr9:138669221 C>T maps to ENST00000298480 Y796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr9:138676391 G>A maps to ENST00000298480 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr8:36694321 A>G maps to NM_001031836.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr8:36642080 T>C maps to NM_001031836.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr8:36721927 C>A maps to NM_001031836.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr8:36671861 G>T maps to NM_001031836.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr16:67327472 C>T maps to NM_001100915.1 W731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:23405540 C>T maps to NM_001009999.2 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr19:5131426 G>A maps to NM_015015.2 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr9:6805636 T>G maps to NM_015061.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:6990510 G>A maps to NM_015061.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr1:202719899 G>A maps to ENST00000367264 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:202702738 C>T maps to ENST00000367264 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:44949045 G>A did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr4:55956203 C>T maps to NM_002253.2 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr4:55961109 G>A maps to NM_002253.2 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr7:142638439 G>A maps to NM_000420.2 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr12:91449806 T>C maps to NM_007035.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:6416894 T>G did not map to a codon.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr1:19563720 C>T maps to NM_015047.1 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr8:126075803 G>C maps to ENST00000377985 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr9:114246645 A>C maps to NM_001080398.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr9:114170942 G>A maps to NM_001080398.1 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr16:27786308 G>A maps to NM_015202.2 V1451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr16:27640071 T>C maps to NM_015202.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr17:2605306 G>A maps to NM_015229.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr1:39876725 A>G maps to NM_015038.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr6:84896079 T>C maps to NM_014895.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr15:79749238 C>T maps to NM_015206.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr4:123166208 C>T maps to NM_015312.3 R1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:123140535 A>G maps to NM_015312.3 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr9:34372001 G>A maps to NM_020702.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr23:118284500 G>A did not map to a codon.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr23:118222474 C>A did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr4:57182124 G>A maps to NM_020722.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr4:57193876 G>A maps to NM_020722.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr10:24833959 C>T maps to NM_019590.3 A1754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:24832987 A>T maps to NM_019590.3 K1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:109707133 C>T maps to NM_020775.3 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr18:34414310 C>T maps to NM_020776.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr1:232941482 C>T maps to NM_019090.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:113761685 C>T maps to NM_020817.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr10:30315251 G>A maps to NM_020848.2 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr10:30318650 G>A maps to NM_020848.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr16:84516257 C>T maps to NM_020947.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:180904727 G>A maps to NM_020950.1 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr2:61315600 A>C maps to NM_001129993.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:73963360 G>T did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr2:8958893 G>A maps to NM_020738.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr1:20992722 G>A maps to NM_020816.2 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:241680732 G>A maps to ENST00000373308 Y1234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:104643665 C>A maps to NM_015656.1 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:245530296 C>T maps to NM_018012.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:69615590 T>G did not map to a codon.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr3:47312945 A>G maps to NM_182902.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr3:47284701 A>G maps to NM_182902.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr1:170003638 T>A did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr13:33591132 G>C maps to NM_004795.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr7:130418290 A>G maps to NM_138693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr4:38690342 G>A maps to NM_016531.5 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr7:129710590 T>G maps to NM_014997.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr1:18808236 C>T maps to NM_152375.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:18809172 G>A maps to NM_152375.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:117043974 C>T did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr23:117032911 T>G did not map to a codon.
Multiple mappings detected for codon TCGA-DU-5855-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr18:30349843 C>T maps to ENST00000426194 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr18:30322012 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-HT-7473-01A-11D-2024-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr18:30349852 C>T maps to ENST00000426194 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:24006739 T>C did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr3:47361234 C>T maps to NM_025010.4 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr15:86312651 G>A maps to NM_022480.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr19:18779268 G>A maps to NM_018316.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr14:45403685 T>C maps to ENST00000355081 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr2:239050039 G>A maps to NM_198582.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr8:124664239 G>A maps to NM_001081675.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr19:51518741 G>A maps to NM_001077500.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr19:51330970 G>A maps to NM_017509.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr19:51330299 G>A maps to NM_017509.2 N105N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E1-5318-01A-01D-1468-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr19:51466621 C>T maps to NM_001012964.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr12:9995005 G>A maps to NM_016523.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr19:10668900 G>A maps to NM_023008.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr7:91865758 T>C maps to NM_194456.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr17:39673185 G>A maps to NM_002275.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr17:38812820 G>A maps to NM_152349.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr17:38857427 G>A maps to NM_019016.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr17:38926338 G>A maps to NM_181539.4 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr17:38936092 G>A maps to NM_181537.3 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr17:38954584 G>A maps to NM_181535.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr17:39553719 G>C maps to ENST00000393998 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr17:39535941 G>A maps to NM_021013.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr17:39596990 G>A maps to NM_006771.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:39595475 G>C maps to NM_006771.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr12:52680929 G>A maps to NM_002281.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr12:52777393 G>A maps to NM_033045.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr21:46057414 C>T maps to NM_181688.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr21:46066416 C>T maps to NM_198692.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr21:46117133 C>T maps to NM_198699.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr21:46011552 A>G maps to NM_198688.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr21:46032409 C>T maps to NM_198695.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr21:46086743 G>A maps to NM_181684.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr21:31798185 G>A maps to NM_181622.1 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:39274306 G>T maps to NM_033059.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:27665527 C>T maps to NM_001168364.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr2:27666915 G>A maps to NM_001168364.1 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr1:52499412 G>A maps to NM_138417.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:153130306 G>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:153133299 G>A did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr18:7036072 G>A maps to NM_005559.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:7023259 C>A maps to NM_005559.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr6:129419502 T>C maps to NM_000426.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr18:21402283 C>T maps to ENST00000416669 Y793Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr18:21425085 T>G maps to ENST00000416669 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr20:60888746 G>A maps to NM_005560.3 D2872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr3:49159714 G>A maps to NM_002292.3 H1554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr9:133942443 C>T maps to ENST00000355048 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:119581703 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr22:33670457 G>A maps to NM_133642.3 Y742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr23:64752491 T>C did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr13:21563345 G>A maps to NM_014572.2 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr13:21549239 G>A maps to NM_014572.2 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr2:30457269 G>T did not map to a codon.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr20:36983810 T>A did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:152671571 C>T maps to NM_178428.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:152671461 C>T maps to NM_178428.3 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:65637237 T>C maps to NM_014319.4 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr7:127892091 C>T maps to NM_000230.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr4:1824792 C>T maps to NM_012318.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr8:38250440 C>T maps to ENST00000379957 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr8:38261999 G>A maps to ENST00000379957 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr22:37966743 T>C did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr17:76967756 C>T maps to NM_005567.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:39299581 G>A maps to NM_006149.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:18396172 G>A maps to NM_001040078.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr12:71978153 C>G maps to NM_003667.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:111914406 G>C did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:111914413 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr13:108861246 T>C maps to NM_001098268.1 E790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr19:55086780 G>A maps to NM_001130917.1 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:55112236 C>T maps to NM_006863.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:54849685 G>A maps to NM_012276.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:54778557 G>A maps to ENST00000391747 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:54780126 C>A maps to ENST00000391747 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:54746594 C>T maps to ENST00000407860 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr19:55178178 C>T maps to ENST00000391733 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr12:50598435 G>A maps to NM_001113546.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:41646514 A>C did not map to a codon.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr22:31663037 G>A maps to NM_001031801.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:128399629 G>A maps to NM_017980.4 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr1:151774673 T>C maps to NM_001004432.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr19:42930578 A>T maps to NM_005357.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:42912408 G>A maps to NM_005357.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr17:73567817 G>A maps to NM_001031803.1 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr3:8590438 C>T maps to NM_014583.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr3:197707306 C>T maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr9:129453249 C>T maps to NM_001174147.1 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr1:13183412 G>A maps to NM_001136561.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr1:13183257 T>C maps to NM_001136561.2 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr1:12908010 C>T maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:118123489 C>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr10:100012143 G>A maps to NM_032211.6 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr10:100013488 C>T maps to NM_032211.6 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr6:161006127 C>T maps to NM_005577.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr6:161027641 A>G maps to NM_005577.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:78010567 A>G did not map to a codon.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr1:82456735 T>C maps to ENST00000370717 N1444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:99753519 G>C did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:39798914 G>C maps to NM_020862.1 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:59272813 A>C maps to NM_153377.3 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr12:59271320 C>T maps to NM_153377.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr12:59276786 G>A maps to NM_153377.3 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr10:86001153 C>T maps to NM_015613.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr2:141128327 A>G maps to NM_018557.2 D3653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr2:141607788 G>A maps to NM_018557.2 D1607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:141816538 G>A maps to NM_018557.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr2:170112637 C>T maps to NM_004525.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr2:170038747 C>T maps to NM_004525.2 Q3309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:170060606 G>A maps to NM_004525.2 T2630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr11:46903300 G>A maps to ENST00000256991 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:46893135 G>A maps to ENST00000256991 L1589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr21:45876869 C>T maps to NM_030891.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr3:169572754 C>T maps to NM_024727.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:76371898 G>C maps to NM_001128922.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr11:76371009 G>A maps to NM_001128922.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr17:45127106 C>G did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr17:45127106 C>G did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr17:45127271 A>C did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr17:45127106 C>G did not map to a codon.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr7:127670471 G>A maps to NM_022143.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr7:127668929 G>C maps to NM_022143.4 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr12:122684843 G>A maps to NM_001098519.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr11:40137056 G>C maps to NM_020929.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:70504173 G>A maps to NM_020794.2 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr1:90048482 C>T maps to NM_015350.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:90400075 C>T maps to NM_001134479.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr12:85518291 A>G maps to NM_001079910.1 E1334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr1:74507114 T>C maps to NM_001105659.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr3:169540470 C>T maps to NM_001080460.1 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr15:101588787 A>G maps to NM_024652.3 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr2:77746148 C>T maps to NM_001134745.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:74969479 G>A maps to NM_000428.2 P1682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr19:41125345 G>T maps to ENST00000308370 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr15:41796599 G>A maps to NM_002344.5 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:144171326 A>C maps to NM_032860.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:114541267 G>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr6:31644772 G>A maps to NM_025262.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr1:160783601 C>T maps to ENST00000263285 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr19:42341279 T>G maps to NM_173506.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr7:20198441 G>T maps to NM_182762.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr1:39900288 A>G maps to ENST00000361689 Q3861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:35802841 C>T maps to NM_002361.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr23:148798318 C>T did not map to a codon.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr23:151896588 C>A did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:151900224 G>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:151896272 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:151935720 A>G did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:151870193 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:149013641 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:30269582 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:27840124 C>T did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:35820490 A>T did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:35820626 C>T did not map to a codon.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr23:35821246 G>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:30237370 A>T did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:30237646 C>T did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:30260294 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:26212349 C>T did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:140996035 T>C did not map to a codon.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr23:140995928 C>T did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:140995654 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:140996472 G>A did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:140994427 C>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:140995061 T>C did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:141290651 T>A did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:141291733 T>C did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:140969495 C>A did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:75649857 T>C did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:75004653 C>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:75003754 A>C did not map to a codon.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr15:23890477 A>G maps to NM_019066.4 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:77998516 G>C maps to NM_012301.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr1:114225639 A>G maps to NM_001142782.1 E1150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:49022445 G>A did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr8:33356081 C>A maps to NM_032509.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr9:72724720 G>A did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:95826018 G>A maps to NM_032427.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:149638920 C>G did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:149638128 T>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:149638771 G>A did not map to a codon.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr9:139996093 C>T maps to NM_016219.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:12768301 G>A maps to NM_000528.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr4:6599986 G>A maps to NM_015274.1 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr4:6612959 C>T maps to NM_015274.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:12483293 C>T maps to NM_018050.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr19:17845206 C>T maps to NM_018174.4 D1050D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr17:67513025 C>A maps to NM_002758.3 C38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr12:53877508 T>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr3:185161415 A>G maps to NM_004721.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr17:61765934 C>T maps to NM_203351.1 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr6:136682202 C>T maps to NM_001198609.1 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr6:136710580 T>A maps to NM_001198609.1 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:20044026 G>A did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:135323364 T>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:135313708 A>G did not map to a codon.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr16:30134371 G>A maps to NM_002746.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr1:206904036 A>C maps to NM_032960.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr4:164450154 G>C maps to ENST00000514618 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr17:60879009 A>G maps to NM_152598.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:58152526 G>A maps to NM_138396.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:220831177 T>G did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr1:220791710 T>C maps to NM_018650.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr11:63667347 A>G maps to NM_001039469.2 A178A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr6:29454623 G>A maps to NM_052967.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr1:46497239 C>A maps to NM_015112.2 S1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr19:18248096 G>A maps to NM_015016.1 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr5:66448609 G>A maps to NM_001164664.1 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr20:3841976 A>G did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:131524901 C>G did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:131520819 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr22:43529108 G>A maps to NM_173467.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr5:112439957 G>T maps to NM_001085377.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:182759529 T>C maps to NM_020166.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr23:138678851 T>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:138689853 T>G did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:138711937 T>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr6:100390943 G>A maps to NM_032503.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr3:127337889 C>T maps to NM_004526.2 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr21:47700423 G>A maps to NM_003906.3 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr22:35811940 C>T maps to NM_006739.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr5:94248539 G>T maps to NM_024717.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:119739937 G>A did not map to a codon.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr6:30679447 C>T maps to NM_014641.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr14:47311141 G>T maps to NM_001113498.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr23:153297773 G>A did not map to a codon.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr17:37565971 T>A maps to NM_004774.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:70345936 C>A did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:70351407 C>A did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:70341256 G>T did not map to a codon.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr23:70346298 C>G did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr17:60111220 C>T maps to NM_005121.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr23:40572232 T>C did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:40518770 T>C did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr6:131917228 A>G maps to ENST00000403834 Y957Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr6:131913581 T>C maps to ENST00000403834 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:16687578 C>T maps to NM_004831.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr19:42857650 G>A maps to ENST00000251268 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr6:46801255 G>A maps to NM_005588.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr6:46803178 C>T maps to NM_005588.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:116381016 C>T maps to NM_001127500.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr7:116412044 T>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr14:21971989 G>A maps to NM_019852.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr18:48703395 G>A maps to NM_016626.4 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr19:1556791 C>T maps to NM_001174118.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr17:19290400 G>A maps to NM_001198695.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr15:89453059 C>T maps to NM_005928.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:12071582 C>T maps to NM_014874.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr22:37882151 G>A maps to NM_002405.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:141708342 G>A maps to ENST00000475668 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:99279631 G>A maps to NM_012214.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr10:103577686 C>A maps to NM_012215.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr16:4732910 C>T maps to NM_015246.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr14:39722039 G>A maps to NM_054024.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:222803483 C>G maps to NM_198551.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr1:1563187 C>T maps to NM_080875.2 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8019-01A-21D-2395-08 chr6:31378386 T>C maps to NM_000247.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr22:18301253 C>T maps to NM_015241.2 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr11:12315445 A>G maps to NM_032867.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr22:38323451 G>A maps to NM_033386.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:31473998 C>T maps to NM_005931.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr6:31473466 G>A maps to NM_005931.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:10534971 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr23:38664317 A>T did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr23:107084364 G>A did not map to a codon.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr19:1255052 C>T maps to NM_177401.4 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr17:4797497 T>C maps to NM_153827.4 H900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:2039674 C>T maps to NM_199054.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr19:2043518 G>A maps to NM_199054.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:28023586 G>A maps to NM_173576.2 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr4:185650177 T>C maps to NM_024629.3 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr16:74725173 C>T did not map to a codon.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr11:118344300 T>A maps to NM_001197104.1 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr12:49446389 T>C maps to NM_003482.3 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr12:49416132 G>A maps to NM_003482.3 R5448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:49445920 C>T maps to NM_003482.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:104753521 G>A maps to NM_182931.2 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr2:238449503 C>T maps to NM_024101.5 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr1:2529662 G>A maps to NM_033467.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:2541235 C>T maps to NM_033467.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:135047267 G>A did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr11:102666336 C>T maps to NM_002421.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr11:102649941 A>G did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr12:132329881 G>T maps to NM_016155.4 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr11:102465487 C>G maps to NM_004771.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr20:33862231 C>T maps to NM_006690.3 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:90833187 A>G maps to NM_007351.2 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:108773664 T>A maps to NM_014429.3 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr22:31330833 A>C maps to ENST00000397641 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:106185948 T>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:106224615 C>A did not map to a codon.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:102931855 T>C did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr12:122091088 G>A maps to NM_173855.4 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr9:13206052 C>A maps to ENST00000319217 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr13:20221184 C>T maps to ENST00000414242 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr17:56357984 G>A maps to ENST00000340482 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr17:56355275 G>A maps to ENST00000340482 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr10:28414005 C>T maps to NM_173496.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr10:28345528 T>C maps to NM_173496.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr1:161275671 C>T maps to ENST00000360451 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr6:84799070 G>A maps to NM_138409.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:19077574 G>A maps to NM_054030.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr11:18195378 T>C maps to NM_054032.3 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr3:131190116 A>C maps to ENST00000425847 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr11:60183352 T>C maps to NM_032597.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr11:59830059 G>A maps to NM_006138.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:60068529 G>C maps to NM_148975.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr11:60107364 T>A maps to NM_139249.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr11:60150652 C>T maps to NM_206939.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:60152679 T>C maps to NM_206939.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:814960 G>A maps to NM_013404.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr8:16026363 C>T maps to ENST00000445506 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr3:49726194 T>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:131208174 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:154293906 T>C did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr15:65312541 C>T maps to NM_139242.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr22:30416521 C>T maps to NM_021090.3 C958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr11:92714796 T>C maps to NM_005959.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr6:74183325 G>A maps to NM_001123226.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr1:11184640 C>T maps to NM_004958.3 L2192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr10:30653857 A>C maps to ENST00000358107 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:17581235 T>G maps to NM_001001924.2 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr19:9069715 A>C maps to NM_024690.2 T5910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr19:9082769 A>G maps to NM_024690.2 T3015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:9089903 G>A maps to NM_024690.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr19:9046746 T>A maps to NM_024690.2 P11628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:9070399 G>A maps to NM_024690.2 P5682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr19:9068569 T>A maps to NM_024690.2 T6292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:8987332 G>A maps to NM_024690.2 T13918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:9089321 C>T maps to NM_024690.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:9087884 A>G maps to NM_024690.2 P1310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr19:9069934 G>T maps to NM_024690.2 P5837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr19:9088745 T>C maps to NM_024690.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr19:9075049 T>A maps to NM_024690.2 S4132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:100677936 T>C maps to NM_001040105.1 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr7:100696422 G>C maps to NM_001040105.1 V4420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:100679592 A>G maps to NM_001040105.1 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr7:100676699 C>A maps to NM_001040105.1 S668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr7:100677106 G>T maps to NM_001040105.1 G804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:1102175 C>T maps to ENST00000441003 H2604H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:1080293 C>T maps to ENST00000441003 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr3:195516419 C>T maps to NM_018406.5 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr3:195515510 G>A maps to NM_018406.5 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr3:195488979 C>T maps to NM_018406.5 Q4830Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr11:1268696 C>T maps to ENST00000447027 T3532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:1265831 C>G maps to ENST00000447027 V2577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr11:1025337 G>A maps to NM_005961.2 N943N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr23:105449890 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:105449980 T>C did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr21:42774041 C>T maps to NM_002463.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr21:42749751 A>T maps to NM_002463.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:3228181 C>T did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:3240115 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:3228241 G>A did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr23:3239836 T>C did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:3229517 C>T did not map to a codon.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr23:3238336 C>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr23:3241680 C>T did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:135522781 A>G maps to NM_001130173.1 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr13:77807396 G>C maps to NM_015057.4 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:81111279 T>C maps to NM_005593.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr17:8424574 G>A maps to ENST00000360416 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:8379259 A>C maps to ENST00000360416 G1962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr17:10223517 G>A maps to NM_003802.2 D1100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr19:50750372 G>A maps to NM_001145809.1 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr17:10370010 G>A maps to NM_017533.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr14:23855274 G>A maps to NM_002471.3 I1675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr14:23884932 A>G maps to NM_000257.2 L1688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr20:33567543 G>A maps to NM_020884.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr17:10297736 C>T maps to NM_002472.2 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:10303715 G>A maps to NM_002472.2 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr17:10299696 G>A maps to NM_002472.2 Q1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:10299868 C>T did not map to a codon.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr20:35177630 C>T maps to NM_006097.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr3:123419710 G>A maps to NM_053025.3 D868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr17:18023394 C>T maps to ENST00000205890 H427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr12:57423553 G>A maps to NM_005379.2 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr10:26500780 G>A maps to NM_017433.4 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr10:26359113 T>C maps to NM_017433.4 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr10:26432480 A>G maps to NM_017433.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr15:52622645 G>A maps to ENST00000358212 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr18:47383223 T>G maps to NM_001080467.2 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:52534267 G>A maps to NM_018728.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr11:76922333 G>A maps to NM_000260.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr15:72122613 T>C maps to ENST00000424560 P2363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr15:72172771 G>A maps to ENST00000424560 N1913N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr15:72190410 A>T maps to ENST00000424560 L1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr17:12655918 T>A maps to NM_001146312.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:12655843 G>A maps to NM_001146312.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr10:95072806 G>A maps to NM_013451.3 Y1953Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:95095761 G>A maps to NM_013451.3 G1493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr18:3135614 G>A maps to NM_003803.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr8:2040225 G>A maps to NM_003970.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr8:2027639 G>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr8:2048768 C>T maps to NM_003970.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr5:150050052 G>A maps to NM_133371.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr19:46394510 C>T maps to NM_001012643.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr20:62839581 G>T maps to NM_004535.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr20:62839767 C>T maps to NM_004535.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:1843078 G>A maps to ENST00000399161 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr2:1906993 C>T maps to ENST00000399161 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr2:1926214 C>T maps to ENST00000399161 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr13:33017398 C>T maps to NM_033111.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr5:177547252 G>A maps to NM_015111.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:153195615 T>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:153195524 T>C did not map to a codon.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr4:140262068 G>A maps to NM_057175.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:63721926 G>C maps to NM_024771.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr12:57487217 G>A maps to NM_005967.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:57487286 A>G maps to NM_005967.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr1:1686108 C>T maps to ENST00000344463 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr17:40695938 G>T maps to NM_000263.3 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr16:5081776 T>C maps to NM_016256.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr5:70405048 C>T did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr12:76453622 C>T maps to NM_139207.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:92927162 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr2:73927952 A>C maps to NM_016347.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr4:2065802 C>G maps to ENST00000423729 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr11:19970368 C>T maps to ENST00000396087 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr12:78513089 T>G maps to NM_014903.4 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr2:15523365 T>C maps to NM_015909.2 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr13:35923242 A>G did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:19981873 A>C maps to NM_182744.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr11:113076287 G>A maps to ENST00000316851 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:19337661 G>A maps to NM_004386.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr12:6635635 C>G maps to NM_014865.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr22:50956004 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr7:74203028 G>A maps to NM_000265.4 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:183543622 C>T maps to NM_001127651.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr3:136646966 C>T maps to NM_006153.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr2:183829475 T>C maps to NM_205842.1 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr12:54917242 G>A maps to NM_005337.4 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr2:133721291 C>T did not map to a codon.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr20:46267763 C>G maps to NM_181659.2 S842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr17:15978995 C>T maps to ENST00000395857 Q1190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:124826570 C>T maps to NM_006312.4 P1669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr12:124810103 G>A maps to NM_006312.4 P2470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:15758700 G>A maps to NM_001143979.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr9:140110622 A>G maps to NM_001144026.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:21486615 C>T maps to NM_201537.1 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr5:149927940 C>T maps to NM_001543.4 H769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr2:152406212 A>G maps to NM_001164507.1 Y6662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:152342396 C>T maps to NM_001164507.1 V8485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr2:152534213 G>A maps to NM_001164507.1 V1213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr2:152409935 C>T maps to NM_001164507.1 K6569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:72163700 A>G maps to NM_173808.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr4:170428877 G>A maps to ENST00000507142 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr3:27352498 G>A maps to ENST00000396636 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr17:27068157 C>T maps to NM_178170.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr17:27065005 C>T maps to NM_178170.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr14:75574124 C>T maps to NM_033116.4 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr12:45000950 C>T did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr15:73541989 C>T maps to NM_002499.3 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr1:156642350 T>C maps to NM_006617.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr2:242755716 C>T maps to NM_001167599.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr4:113436145 C>T maps to NM_024019.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr17:29563006 G>A maps to NM_001042492.2 W1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr17:29552215 T>A maps to NM_001042492.2 L650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:29497015 G>A did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr17:29670154 T>A did not map to a codon.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr17:29553696 C>A maps to NM_001042492.2 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr17:29663349 G>C did not map to a codon.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr17:29663746 T>G maps to NM_001042492.2 L2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr17:29576000 G>A did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr17:29664445 T>A maps to NM_001042492.2 L2163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:204946827 T>A maps to ENST00000367172 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr16:69689702 G>A did not map to a codon.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr18:77227574 C>T maps to NM_172387.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr20:50091993 C>T did not map to a codon.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr7:26224961 T>C maps to NM_004289.6 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr14:35872894 C>T did not map to a codon.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr4:47850314 A>T maps to NM_152995.4 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr12:104517156 C>T maps to NM_006166.3 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr14:23940134 A>G maps to NM_001042635.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:17394315 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:17744929 G>T did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr14:52520996 G>A maps to NM_007361.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:674454 G>A maps to NM_016533.4 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr20:25436317 C>T maps to NM_025176.4 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr20:25436401 C>T maps to NM_025176.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr4:48037777 G>T maps to NM_207330.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:37008731 C>G maps to NM_133433.3 S1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr5:36961656 C>T maps to NM_133433.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:36985703 C>T maps to NM_133433.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr9:107513271 C>T maps to NM_015469.1 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr3:52489674 C>T maps to NM_007184.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:119077533 C>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:119070600 C>A did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr6:28228313 C>T maps to NM_001007531.1 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr6:28228258 A>G maps to NM_001007531.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:118724015 T>C did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:36987092 G>T maps to NM_001079668.2 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr14:37051528 C>T maps to NM_014360.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:13543757 G>C maps to NM_001189.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:70367669 T>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:70389236 C>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:70387551 G>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:5811259 C>T did not map to a codon.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr2:32449595 A>G maps to NM_021209.4 F1007F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:32476670 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr2:32461394 G>A maps to NM_021209.4 H845H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr19:54299147 C>G maps to ENST00000391773 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr19:56421927 C>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:7061016 G>A did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr1:247582221 G>A maps to NM_004895.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:247608069 C>G maps to NM_004895.4 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr19:56369919 C>T maps to NM_134444.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr19:56539140 C>T maps to NM_153447.4 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:56539530 C>T maps to NM_153447.4 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr19:56515294 C>T maps to NM_153447.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr19:56249566 C>A maps to NM_176820.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr5:43613178 A>G maps to NM_182977.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:144096875 G>A maps to ENST00000467773 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:144096158 G>A maps to ENST00000467773 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr18:31709957 T>C maps to NM_003787.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr12:117705871 A>G maps to ENST00000338101 N639N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr12:117768409 G>A maps to ENST00000338101 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr12:117669889 G>A maps to ENST00000338101 T1128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr17:26116670 G>A maps to NM_000625.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr9:139412202 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:139401405 G>A maps to NM_017617.3 N1221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr9:139395300 T>G did not map to a codon.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:120502126 T>C did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:15299836 G>A maps to NM_000435.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:32188017 G>T maps to NM_004557.3 C401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:32166812 G>A maps to NM_004557.3 R1475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:32190324 C>T maps to NM_004557.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr15:69348972 G>A maps to NM_024505.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:34263251 T>G did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr11:108043928 A>G maps to NM_002519.2 N594N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr8:53852886 C>T maps to NM_005285.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr18:21114451 G>A maps to NM_000271.4 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr7:44579719 G>A maps to NM_013389.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:72994631 A>T maps to NM_004885.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr19:36340182 G>A maps to NM_004646.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr16:15026512 C>T maps to ENST00000435714 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:153655964 C>T maps to NM_000906.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr1:153654205 C>T maps to NM_000906.3 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:32739000 C>T maps to ENST00000265074 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr7:34724168 G>A maps to NM_207172.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr7:24329162 G>A maps to NM_000905.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr4:164247118 G>A maps to NM_000909.4 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:164271442 C>T maps to NM_006174.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:15065636 T>A maps to NM_003298.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:105178374 T>A did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:105167162 C>T did not map to a codon.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr2:50723229 G>C maps to ENST00000404971 Y1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr23:152034374 G>A did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:152037636 C>T did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:1445044 G>A maps to ENST00000476071 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr12:5603653 C>T maps to NM_001102654.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr12:5603796 C>T maps to NM_001102654.1 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:2522816 C>T maps to NM_006181.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr1:156841488 G>A maps to NM_002529.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:11798781 A>T maps to NM_012344.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr19:49422369 G>T maps to NM_006184.5 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:51075879 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:21965731 C>T maps to NM_024815.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr11:71725527 C>T maps to ENST00000393695 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr6:17629744 C>T maps to ENST00000430136 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr9:131768628 G>A maps to NM_015354.1 Q1685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:135298929 C>T maps to NM_015135.2 C1073C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:153995730 G>A maps to NM_207308.2 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr9:134073212 A>G maps to ENST00000451030 Q1445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:5312117 T>A maps to NM_002532.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr19:16860739 C>T maps to ENST00000438489 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr19:16874670 G>A maps to ENST00000438489 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr23:102338547 C>T did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr14:24884569 G>A maps to NM_025081.2 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr1:228529313 G>A maps to NM_001098623.1 W6011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr2:220432494 G>A maps to NM_015311.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr8:133044198 C>T maps to ENST00000262283 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr15:28235790 G>A maps to NM_000275.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:128692668 C>A did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:128710472 C>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:10582005 G>A maps to NM_002539.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr23:123654450 C>T did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:123680891 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:123525988 A>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:123785902 C>T did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:123785887 G>A did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:123525931 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:123519790 C>A did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:123517775 G>A did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:123518057 C>T did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:123519690 G>C did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr4:183609325 T>C maps to NM_001080477.1 C681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr11:78369774 T>C maps to NM_001098816.2 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:13786332 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr6:72011296 C>T maps to NM_024576.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:70784540 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:70793626 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:70776955 G>T did not map to a codon.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr23:70767812 T>G did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr10:74673064 G>C did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr19:9965170 C>T maps to NM_058164.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr13:53624245 G>A maps to NM_006418.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr11:132527045 C>T maps to NM_002545.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:67283789 G>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:67414333 G>C did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:67413795 T>C did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:153416329 C>T did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr10:88418310 C>T maps to NM_001030015.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr10:88418274 T>C maps to NM_001030015.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr6:47754300 C>T maps to ENST00000489301 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr11:123886715 C>T maps to NM_001004462.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr11:123909444 G>C maps to NM_001004463.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:123909048 G>A maps to NM_001004463.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr11:123901192 C>T maps to ENST00000375021 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:15918655 G>A maps to NM_013940.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr1:159283477 C>T maps to NM_001004467.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:158449813 A>G maps to NM_001004472.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:20666310 A>T maps to NM_001005503.1 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr10:45799360 G>A maps to NM_001004297.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr9:107298218 C>T maps to NM_001001961.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr9:107331777 G>A maps to NM_001004483.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:247835491 C>T maps to NM_001005487.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr1:247835569 G>T maps to NM_001005487.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr17:3119150 T>C maps to NM_014565.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr17:3119138 G>A maps to NM_014565.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr17:3100859 A>G maps to NM_012352.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr9:125273991 C>A maps to NM_054107.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:9204447 C>T maps to ENST00000305465 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr11:6789588 G>A maps to NM_001004490.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr6:27925798 C>T maps to NM_012367.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr1:247769423 C>T maps to NM_001001914.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:248685219 C>T maps to NM_001013355.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:248685543 C>T maps to NM_001013355.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:248112251 T>C maps to NM_001001963.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr1:248309135 A>T maps to NM_001004690.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr1:248570029 C>T maps to NM_030904.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr1:248789592 C>T maps to NM_001001964.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:248458715 C>T maps to NM_001004692.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:248616319 C>T maps to NM_001004136.1 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:248637421 C>T maps to NM_001005495.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:248737287 G>A maps to NM_001001821.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:248084418 T>C maps to NM_001005522.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr5:180166656 G>T maps to NM_001001657.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr19:8841994 C>A maps to NM_001004699.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr17:3181605 G>A maps to NM_002551.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr11:55136012 C>A maps to NM_001005275.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr11:55110939 C>T maps to NM_001005274.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr11:51411930 C>T maps to NM_001005272.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr11:49974105 G>T maps to NM_001001955.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr11:55339752 C>T maps to NM_001004701.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr11:59224534 G>T maps to NM_001004708.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr14:20345253 C>A maps to NM_001005501.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr11:55406510 C>A maps to NM_001004124.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:48286041 C>T maps to NM_001004726.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:48266711 C>T maps to NM_001004727.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:48266882 T>C maps to NM_001004727.1 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr11:4842845 C>T maps to NM_001004753.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:4944909 G>A maps to NM_001005237.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:5020871 T>C maps to NM_001004755.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr11:5021018 T>C maps to NM_001004755.1 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr11:4388940 T>C maps to NM_001005161.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr11:5906224 C>T maps to NM_001005165.1 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:5878263 A>C maps to NM_001005168.1 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr11:6023640 G>A maps to NM_001005179.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr11:5989292 G>A maps to NM_001146033.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr11:59132062 C>T maps to NM_001004729.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr11:55563531 G>T maps to NM_001004735.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr11:55587485 T>A maps to ENST00000395203 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:55587451 T>G maps to ENST00000395203 L118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr3:97887872 A>T maps to NM_001005515.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr3:97983514 T>C maps to NM_001005479.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr11:56237958 G>A maps to NM_001004742.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr11:56258828 C>T maps to NM_001005282.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:56185614 A>G maps to NM_001004744.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr1:247875305 C>T maps to NM_001005286.1 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr11:123676271 G>A maps to NM_001005325.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr11:57798999 G>A maps to NM_001005186.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:15052350 C>T maps to NM_012377.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr19:9296886 C>T maps to NM_175883.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr11:55861307 T>C maps to NM_001003750.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr11:55861580 G>A maps to NM_001003750.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr11:55904471 G>A maps to NM_001004064.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr11:56086682 C>T maps to NM_001005202.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr7:142723664 G>A maps to NM_001001658.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:56511044 C>G maps to NM_001005284.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr11:56510828 G>A maps to NM_001005284.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr11:56468237 C>T maps to NM_001013358.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr7:102087147 G>A maps to NM_032831.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr5:38923282 C>T maps to NM_003999.2 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr8:99962882 G>A did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr9:77752521 T>G maps to NM_012383.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:26700617 C>T maps to NM_194322.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr4:4214702 G>A maps to NM_177998.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr2:241079505 C>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr4:146058890 A>C maps to ENST00000447906 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:48791844 G>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr17:1946241 G>A maps to NM_080822.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr3:25833093 C>T maps to NM_017897.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr11:72945404 G>A maps to NM_176071.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr12:56504239 C>T maps to NM_006191.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr12:56501318 A>G maps to NM_006191.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr12:56504344 C>T maps to NM_006191.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:20715161 C>T maps to ENST00000503585 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:34498364 G>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr11:47202191 C>T maps to NM_016223.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr1:17418909 G>A maps to NM_007365.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:49455851 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:110385327 T>C did not map to a codon.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr16:23646264 A>G maps to NM_024675.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr9:112900625 C>T maps to NM_007203.4 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr9:112898642 C>T maps to NM_007203.4 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:119097281 C>A maps to NM_002581.3 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:176525626 C>T maps to NM_020318.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr3:183580580 C>T maps to NM_018622.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:145058233 G>A maps to NM_032789.3 N573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr14:20818732 G>T maps to NM_005484.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr22:44489820 G>A maps to NM_001003828.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr23:150793998 T>C did not map to a codon.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr3:52621371 G>C maps to ENST00000296302 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr3:52643531 T>A maps to ENST00000296302 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr3:52597304 G>A maps to ENST00000296302 P1360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr6:32157563 C>A maps to NM_002586.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr19:19672910 G>A maps to NM_025245.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:91090534 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:91133711 G>A did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:91090709 C>T did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr23:91133910 C>A did not map to a codon.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr23:91133711 G>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr24:5369104 G>T did not map to a codon.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr24:5605957 C>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:99662057 C>A did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:99662275 G>A did not map to a codon.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr23:99551564 G>A did not map to a codon.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr23:99662027 T>C did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:99661765 G>A did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:99662609 T>C did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:99662600 A>G did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr13:61986932 G>A maps to NM_022843.3 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr4:30723436 C>G maps to NM_001173523.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr13:67800157 T>C maps to NM_203487.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr5:140249977 T>C maps to NM_018902.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr5:140176069 C>T maps to NM_018905.2 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr5:140181906 C>T maps to NM_018906.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:140214297 G>T maps to NM_018910.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:140182209 G>T maps to NM_018906.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr5:140263553 G>A maps to NM_018904.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr5:140237336 C>G maps to NM_018901.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:140182695 C>T maps to NM_018906.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:140176510 C>T maps to NM_018905.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr5:140474487 C>T maps to NM_018936.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr5:140475879 C>T maps to NM_018936.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr5:140502917 C>T maps to NM_018938.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr5:140710808 C>T maps to NM_018912.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr5:140746017 C>T maps to NM_018918.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:140801468 C>T maps to NM_018914.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr5:140724037 G>A maps to NM_018916.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:140736509 C>T maps to NM_018917.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr5:140755692 C>T maps to NM_018919.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr5:140718978 G>T maps to NM_018915.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr5:140711255 C>A maps to NM_018912.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr5:140762774 G>A maps to NM_018920.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr20:44567655 C>T maps to NM_022104.3 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:82785656 C>T maps to NM_033026.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:82583260 G>A maps to NM_033026.5 S2336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr7:82583284 G>A maps to NM_033026.5 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr8:17794713 T>C maps to NM_006197.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr8:52733123 A>T maps to NM_052937.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr21:47845845 C>T maps to NM_006031.5 D2427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr14:71443879 A>T maps to NM_014982.2 K276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr1:233150466 G>C maps to NM_014801.3 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:233150465 G>A maps to NM_014801.3 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr20:17339013 C>T maps to NM_002594.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr9:78965753 G>A maps to NM_001190482.1 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:78943021 C>T maps to NM_001190482.1 N1452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr15:101971659 G>A maps to NM_002570.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr1:55523125 C>T maps to NM_174936.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr2:70504433 C>T maps to NM_016297.3 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:105184817 G>A maps to NM_014976.1 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:178682595 G>A maps to NM_016953.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr2:183095780 A>C maps to NM_005019.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr11:72289380 C>T maps to NM_002599.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr19:18329191 G>A maps to NM_000923.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr1:144856851 C>T maps to NM_014644.4 A2211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr4:619540 G>A maps to NM_000283.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr4:663880 C>A maps to NM_000283.3 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:659048 A>G maps to NM_000283.3 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr10:95385364 G>T maps to NM_006204.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:76649191 G>A maps to NM_003719.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr11:103870851 G>A maps to NM_025208.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr4:55139757 C>T maps to NM_006206.4 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:19368153 C>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:19368117 G>C did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:19369426 G>A did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr4:96761528 A>G maps to NM_005390.4 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr2:10929976 G>A maps to ENST00000381611 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr16:20387484 G>A maps to NM_174924.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:24545691 A>T did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr5:176918074 C>T maps to NM_005451.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr16:66919575 C>T maps to NM_020786.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr16:66919404 C>T maps to NM_020786.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:153069773 G>T did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:153069211 C>T did not map to a codon.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr1:160181385 G>T maps to ENST00000368075 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:32101081 C>T maps to NM_012392.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:66243520 C>A maps to NM_145065.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:4578456 C>G maps to ENST00000301396 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:7362770 C>T maps to NM_001131023.1 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr12:53689234 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr1:207252342 G>A maps to NM_001018053.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr10:6257193 C>G maps to NM_004566.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:77380494 C>T did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr6:49754105 G>A maps to NM_138733.4 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:46522886 G>A maps to NM_005091.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr19:15586703 C>T maps to NM_052890.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr1:153315566 T>C maps to NM_020393.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr1:64100509 G>A maps to NM_002633.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr11:74085468 C>T maps to NM_173582.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:100998772 C>A maps to NM_000926.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:118370560 C>T did not map to a codon.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr20:58349321 G>A maps to NM_080672.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:33837952 G>A maps to ENST00000419414 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr3:169835094 A>G maps to NM_024947.3 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr3:169815125 T>C maps to NM_024947.3 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:22095666 T>A did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr1:6681633 C>G maps to NM_153812.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr5:133914910 C>T maps to ENST00000448712 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:46884201 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr23:46887418 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:129782914 C>T maps to NM_199320.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr17:7139546 T>C maps to NM_024297.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr6:64394226 C>T maps to NM_015153.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr6:64423123 C>G maps to NM_015153.2 G1880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:133527973 A>G did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:79650980 G>C maps to NM_017934.5 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:18912470 G>C did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:18924630 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr16:47694708 C>T maps to NM_000293.2 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr11:608554 G>A maps to ENST00000264555 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr10:61007533 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr22:21083937 C>T maps to NM_058004.2 T1432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr13:73505356 A>G maps to NM_006346.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr4:527752 G>A maps to NM_001127178.1 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr9:35093983 G>A maps to NM_032634.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr17:26890905 G>A maps to NM_033198.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr19:49954794 C>A maps to NM_017916.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr5:67569269 G>A maps to ENST00000396611 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr19:18272832 C>T maps to NM_005027.2 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr17:8794081 G>A maps to NM_001142633.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr17:8741185 C>T maps to NM_001010855.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr12:57989813 G>A maps to NM_024779.4 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr11:67269772 C>T maps to NM_004910.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:123473363 G>A maps to NM_020845.2 D929D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr17:6381926 T>A maps to NM_031220.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr5:134364858 G>A maps to NM_002653.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr22:25119190 G>A maps to NM_001008496.2 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr16:2164290 C>A maps to NM_001009944.2 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr16:2161834 G>A maps to NM_001009944.2 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr16:2147948 G>A maps to NM_001009944.2 Q3363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr16:2139949 G>A maps to NM_001009944.2 N4230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr7:47840378 G>A maps to NM_138295.3 P2687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr10:102057296 G>A maps to NM_016112.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr6:51882308 C>T maps to NM_138694.3 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:51799070 G>A maps to NM_138694.3 H1986H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr8:110468611 A>G maps to ENST00000426474 T2332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr9:131475881 G>C maps to NM_013355.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr1:201282316 G>A maps to NM_000299.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr12:32974415 G>A maps to NM_004572.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr2:159537146 T>C maps to NM_003628.3 Y1179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr15:42371770 C>G maps to NM_178034.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr15:42434837 G>A maps to ENST00000397272 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr2:160832716 A>G maps to NM_007366.4 Y819Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:133700589 G>C did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr10:81901856 T>A maps to NM_001012973.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr8:57079206 G>A maps to NM_002655.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr10:75675024 G>A maps to NM_002658.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:28785935 C>T maps to NM_153021.4 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:113824840 C>T maps to NM_173542.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:8665705 G>A maps to NM_015192.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:219500984 G>C maps to ENST00000432688 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr10:95790841 T>C maps to ENST00000371380 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:81925183 G>A maps to NM_002661.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:155198969 G>A maps to ENST00000340059 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr5:41381989 G>T maps to NM_001005473.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:40883896 C>G maps to NM_012268.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr14:105399117 G>A maps to NM_138790.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:144995969 C>T maps to NM_201380.2 A2810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr12:19475546 T>C maps to ENST00000429027 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr7:30092390 C>T maps to ENST00000440706 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr6:151054743 T>C did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr5:161917 A>G maps to NM_052909.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr1:907740 C>T maps to ENST00000379409 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr6:161173246 C>T maps to NM_000301.3 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr9:19116569 G>A maps to NM_001122.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr19:4511094 G>A maps to NM_001080400.1 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr19:4511136 G>A maps to NM_001080400.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:12024321 C>T maps to ENST00000376369 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:103043373 C>T did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:114882252 T>G did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:153695647 G>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:153688766 A>G did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:153698492 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr23:153693429 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:131848963 G>A maps to NM_020911.1 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr7:131848942 G>A maps to NM_020911.1 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:153043474 T>C did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:153039466 C>A did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr1:205814451 C>G did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:72166637 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr15:74290532 C>T maps to NM_033238.2 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:152226070 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:152226307 G>T did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:152226633 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:152159962 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:152159279 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-FG-8186-01A-11D-2253-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr19:46998155 G>A maps to ENST00000377652 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr14:20940626 C>T maps to NM_000270.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:36262064 C>A maps to ENST00000457797 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:7619473 C>T maps to NM_001166111.1 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr9:140409906 C>T maps to NM_001098537.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr23:84586011 C>T did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr23:84600915 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:84563164 G>A did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:24830875 G>A did not map to a codon.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:24753560 T>A did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:24735545 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:133250238 G>A maps to ENST00000455752 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:133254166 G>A maps to ENST00000455752 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr15:89864981 G>A maps to NM_002693.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr10:103343336 G>A maps to NM_013274.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr3:121186387 T>A maps to ENST00000393672 R2451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:86316950 G>A maps to NM_015425.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:113322006 C>T maps to NM_019014.4 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:57504026 C>T maps to NM_032940.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr19:1090942 C>T maps to NM_002695.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr10:79785905 G>A maps to NM_007055.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr22:41936718 G>A maps to NM_138338.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr7:94947700 G>A maps to NM_000446.5 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr7:94940782 G>T maps to NM_000446.5 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr8:99169862 G>A maps to NM_015029.2 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr7:75601766 G>A maps to NM_000941.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr13:38153416 A>G maps to NM_006475.2 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr13:38171319 C>T did not map to a codon.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr18:14543091 G>A maps to ENST00000444806 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr2:130832725 G>A maps to NM_001099771.2 H773H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr14:19553817 C>T maps to NM_001005356.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr14:19553811 G>A maps to NM_001005356.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr22:16287513 G>A maps to NM_001136213.1 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr19:42600386 G>A maps to ENST00000342301 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr19:10224313 A>T maps to NM_001040664.2 K429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr3:12458612 C>T maps to NM_015869.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr4:23815629 T>C maps to NM_013261.3 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr11:70208263 G>A maps to NM_003626.2 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr12:42835163 G>A maps to NM_016488.6 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr10:81113477 T>C maps to NM_005729.3 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:44457549 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr1:113257683 C>T maps to NM_005167.5 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:45885826 C>T maps to NM_001142502.1 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr20:37536525 C>T maps to NM_015568.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr7:113517990 A>G maps to NM_002711.3 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:49126931 G>A did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:49142308 C>T did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr10:133748025 C>T maps to ENST00000455566 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:68413614 A>G maps to ENST00000406334 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr9:104356876 G>A maps to NM_147180.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr18:9549243 G>A maps to NM_001042388.1 N880N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr10:103899572 G>A maps to NM_015062.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr1:12884886 G>T maps to NM_001146344.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:12837724 C>T maps to NM_001080830.1 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:12943050 C>T maps to NM_001009611.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr11:129784708 G>A maps to NM_020228.2 R915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr8:70978497 C>T maps to NM_024504.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr8:70981759 C>T maps to NM_024504.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr1:14143063 A>G maps to NM_001135610.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr4:121631493 C>T maps to NM_018699.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr16:90124771 G>A maps to NM_001098173.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr5:23527686 G>A maps to NM_020227.2 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:47266678 C>T maps to NM_020820.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr10:72358831 A>C maps to NM_005041.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr11:57144242 G>A did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr1:186276305 T>C maps to NM_005807.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:62193042 A>G maps to NM_001037335.2 A2249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:62195518 C>T maps to NM_001037335.2 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr12:42858962 A>G maps to NM_153026.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr12:42860092 T>A maps to NM_153026.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr6:41753226 C>T maps to NM_013397.5 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr6:57185253 G>T did not map to a codon.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr7:751124 G>C maps to NM_002735.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr17:64785021 G>A maps to NM_002737.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr10:6527129 C>T maps to NM_006257.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr14:30105554 G>A maps to NM_002742.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:82026997 G>A maps to NM_006259.1 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:35065589 C>T maps to NM_000949.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr4:148594114 G>T maps to NM_138364.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr20:4705631 C>T maps to NM_012409.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr19:36302866 C>T maps to NM_021232.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr19:36293162 G>T maps to NM_021232.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:45583421 G>A maps to NM_017922.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr12:50036430 C>G maps to NM_001031698.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr17:1585130 C>T maps to NM_006445.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr17:1557306 C>T maps to NM_006445.3 V1997V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr6:42690066 C>T maps to NM_000322.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr23:106890920 G>A did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:12838860 C>T did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr19:50123628 C>T maps to NM_020719.1 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr19:50100108 A>C maps to NM_020719.1 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr16:30666112 A>C maps to NM_024031.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr16:30664040 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:42814702 G>A maps to NM_199285.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:42813897 G>T maps to NM_199285.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:855738 G>A maps to NM_001013638.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr16:2906138 G>A maps to NM_022119.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:84233952 C>T maps to NM_153362.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr6:84233253 A>T maps to NM_153362.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr3:46755846 G>A maps to NM_013270.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr16:58324918 G>A maps to NM_001080492.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr9:79324330 G>A maps to NM_015225.2 N953N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr8:18725327 G>C maps to ENST00000440756 S497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr8:18729530 T>A maps to ENST00000440756 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr8:18490300 T>C maps to ENST00000440756 K746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr19:43519343 A>G maps to ENST00000306308 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr19:43766010 C>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr17:65341916 T>A maps to NM_002816.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr17:40990762 C>T maps to NM_176863.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr1:97278638 T>A maps to ENST00000370197 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:45291948 G>A maps to NM_003738.4 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:45294291 G>A maps to NM_003738.4 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:23353201 T>G did not map to a codon.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr10:16526577 T>C maps to NM_030664.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr9:130885211 C>T maps to ENST00000492057 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr1:186643727 A>G maps to NM_000963.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:209309553 C>A maps to NM_005048.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr8:141889586 G>A maps to NM_005607.4 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr8:27310643 G>A maps to NM_004103.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr3:47447436 C>A maps to NM_015466.2 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:112166751 G>A maps to NM_002829.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:120709679 A>G maps to NM_002830.2 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr12:70980858 G>A maps to NM_001109754.1 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr12:71002870 C>T maps to NM_001109754.1 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:70949899 G>A maps to NM_001109754.1 C1581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:198687262 A>T maps to ENST00000271610 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr9:8633422 G>A maps to NM_002839.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr9:8376663 C>T maps to NM_002839.3 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:44056970 C>T maps to NM_002840.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr1:44019523 G>A maps to NM_002840.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr3:62248552 C>G maps to NM_002841.3 Y880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr19:55693460 G>A maps to NM_002842.3 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr18:7949177 G>A did not map to a codon.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr12:15654566 T>C maps to NM_030667.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:71094988 G>A maps to NM_002849.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:71094999 G>A maps to NM_002849.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:29585122 C>A maps to NM_005704.4 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr1:29611339 C>T maps to NM_005704.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr7:121693972 C>T maps to NM_002851.2 Q2088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr12:44149036 A>G maps to NM_031292.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr10:134219371 G>A maps to NM_138499.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:1684082 C>T maps to NM_012293.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr8:52233388 G>A maps to NM_144651.4 A1405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr12:133277885 G>A maps to NM_018663.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr14:51378915 G>A maps to NM_002863.4 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr12:21593339 A>G maps to NM_024854.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr12:21615671 A>G did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr10:100143598 G>A maps to NM_032709.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:9317914 G>A maps to NM_002864.2 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr12:9309930 G>A maps to NM_002864.2 A1130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr9:139118661 G>A maps to NM_181701.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr8:37729418 C>T maps to NM_001002814.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr8:37730000 G>A maps to NM_001002814.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr8:37734855 G>A maps to NM_001002814.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr2:238483769 G>A maps to NM_022449.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:129306041 G>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:129318701 C>G did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr17:5257697 A>G maps to NM_004703.4 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:24737795 G>A maps to NM_182836.1 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr5:131930713 T>A maps to NM_005732.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr12:1023181 A>T maps to NM_134424.2 L358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr7:4855892 G>A maps to NM_018059.4 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:12653551 G>A maps to ENST00000415519 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr11:36596674 C>T maps to NM_000448.2 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr11:36614245 G>A maps to NM_000536.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr7:39726380 G>T did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr7:45222923 C>T maps to NM_005856.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr17:2909298 C>T maps to NM_015085.4 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr23:131351244 C>T did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr9:134501729 G>A maps to NM_198679.1 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr4:160277113 G>A maps to NM_014247.2 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr12:53609146 G>A maps to NM_000966.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr7:150037191 A>G maps to NM_002889.3 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr22:35947955 C>T maps to NM_014310.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr15:79277480 G>A maps to NM_002891.4 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:79296192 G>A maps to NM_002891.4 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr5:80366345 A>G maps to NM_006909.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr22:29709886 G>A maps to NM_006477.3 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr1:206711606 C>T maps to NM_182663.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr12:86199244 A>G maps to NM_005447.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr12:86199469 C>T maps to NM_005447.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr13:48953727 A>G did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:94747711 C>G maps to NM_203390.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:150073654 C>T maps to NM_018047.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr7:155530751 A>G did not map to a codon.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr23:106310756 C>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr4:155719189 C>T maps to NM_144979.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:50099411 C>T maps to NM_005777.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr3:29977602 C>T maps to NM_001003793.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr3:29323192 G>A maps to NM_001003793.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr23:135956318 T>C did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr3:139237307 C>T maps to NM_002899.3 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr10:48390166 G>A maps to NM_002900.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr4:26422325 C>T maps to NM_005349.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr20:43945325 G>A maps to NM_014276.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr1:211652455 G>A maps to NM_183059.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr11:110134884 A>C maps to ENST00000405097 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr9:36102222 C>A maps to NM_021111.2 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:1495533 C>T maps to ENST00000395479 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr11:65429216 T>C maps to NM_021975.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr7:103338476 C>T maps to ENST00000428762 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:73102212 C>T maps to NM_152222.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr14:23354153 G>A maps to NM_173527.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:153209005 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:153208401 G>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:153208517 T>G did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:17073014 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:17065568 C>T did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr10:43609022 A>G maps to NM_020975.4 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr10:43622042 G>A maps to NM_020975.4 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr3:108475915 G>T maps to NM_032579.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr6:111726681 T>G maps to NM_002912.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:39306545 C>T maps to ENST00000381897 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:53126462 C>T maps to NM_052859.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr19:14083695 G>C maps to NM_002918.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr19:6013016 C>T maps to NM_000635.3 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr6:117198500 C>T maps to NM_173560.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:117245847 T>C maps to NM_173560.3 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr15:56387425 G>A maps to NM_022841.5 Q834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:109695333 A>T did not map to a codon.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr23:109694415 T>C did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:109696414 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:109698483 G>T did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:109695812 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:109694049 C>G did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:71350422 C>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:71350843 C>T did not map to a codon.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr23:46943842 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:46951572 G>A did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr2:107041182 C>T maps to ENST00000304514 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:321438 C>T maps to NM_183337.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr6:49604489 C>A maps to NM_000324.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr16:111433 G>A maps to NM_022450.3 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr3:129251554 G>A maps to NM_000539.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr10:62648195 A>G maps to NM_014836.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:95119547 C>T maps to NM_014899.3 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr2:152319417 C>T maps to NM_018151.4 D1128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr12:130898839 G>A maps to NM_015347.4 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr20:19945626 C>T maps to ENST00000255006 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:105187663 G>A maps to NM_021930.4 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr21:43161993 G>A maps to ENST00000352483 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr21:43161858 G>A maps to ENST00000352483 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr21:43161011 G>A maps to ENST00000352483 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr6:84567020 G>A maps to NM_001009994.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:73812348 G>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr16:67688718 A>G maps to NM_001013838.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr16:67690170 G>A maps to NM_001013838.1 S1261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr2:86831208 T>C maps to NM_005667.3 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr17:19316086 T>A maps to NM_007148.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr18:29648290 C>T maps to NM_017831.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:105937388 G>A did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr7:122338204 G>A maps to NM_139175.1 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr13:25428133 G>A maps to ENST00000381927 Q1203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr17:78320933 G>A maps to NM_020914.4 A2982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr14:24619440 A>T maps to NM_017999.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr17:56435581 G>A maps to NM_017763.4 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr1:201972431 G>T maps to NM_020216.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr1:201966605 C>T maps to NM_020216.3 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr3:77617552 C>T maps to ENST00000332191 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr3:77614191 C>T maps to ENST00000332191 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr11:62381889 C>T maps to NM_000327.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr5:10461351 C>T maps to NM_031916.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr1:64515591 C>T maps to NM_005012.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:77257631 C>T maps to ENST00000396204 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr9:77277522 G>T did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr6:117609711 A>G maps to NM_002944.2 P2329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:117686237 G>A maps to NM_002944.2 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr8:10470653 G>A maps to NM_178857.5 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr17:1798389 G>A did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr12:48096530 C>T maps to NM_024604.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr16:53679915 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr2:89037525 C>T maps to NM_144563.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr14:47120402 G>A maps to NM_080746.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr9:136217155 C>T maps to NM_000972.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr15:75248607 C>T maps to NM_017793.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:71493767 G>T did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr24:22930743 C>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:20205953 C>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:64137196 C>T maps to NM_003942.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:83319381 A>G did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:83403056 A>G did not map to a codon.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr1:213414639 T>C maps to NM_012424.3 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr1:152129013 T>C maps to NM_001122965.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:837404 G>A maps to NM_058192.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr11:14303173 A>C maps to NM_012250.5 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr6:7229936 G>T maps to NM_001003699.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:18660176 C>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr23:18665416 C>G did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr2:7027290 G>A maps to NM_080657.4 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr1:114308979 G>A maps to NM_018364.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr6:159403543 C>T maps to NM_031924.4 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:116938226 A>G maps to NM_001010892.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr6:43612864 G>A maps to NM_152732.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr18:67695980 A>C maps to NM_173630.3 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr5:179016594 C>T maps to NM_025158.3 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:178996302 C>T maps to NM_025158.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr4:159526261 C>T maps to ENST00000440678 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr4:159533493 A>C maps to ENST00000440678 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr9:137293637 G>A maps to NM_002957.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr1:165389158 G>A maps to NM_006917.4 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr3:133878163 G>A maps to ENST00000296084 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:38942435 C>T maps to NM_000540.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:39039014 C>T maps to NM_000540.2 Y4079Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr1:237957282 C>T maps to NM_001035.2 L4633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr15:33893720 C>G maps to NM_001036.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr1:101705574 C>T maps to NM_001400.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr19:10334890 G>A maps to NM_004230.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:134988649 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:134994994 C>T did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:134992596 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:134988659 G>A did not map to a codon.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr21:15893492 G>T maps to ENST00000285670 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr9:136578199 C>T maps to NM_007101.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr11:65733981 A>G maps to NM_005146.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:128926407 G>A did not map to a codon.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:128914083 G>A did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:23801977 G>A did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:84363188 G>A did not map to a codon.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr22:50898007 G>A maps to ENST00000337034 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:28331419 G>C maps to NM_001024401.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr16:28331452 G>C maps to NM_001024401.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:56041300 C>T maps to NM_001101401.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr12:123834922 G>A maps to NM_001167856.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr19:50156699 A>C maps to NM_021228.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr19:50154596 C>T maps to NM_021228.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr6:28540668 G>A maps to NM_052923.1 C999C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr15:77064286 C>T maps to ENST00000324767 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr10:102112183 C>T maps to NM_005063.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr11:62037738 C>T maps to NM_002411.2 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr1:41579186 C>T maps to NM_001031694.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr3:38739793 G>A maps to NM_006514.2 D1639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr3:38768258 T>C maps to NM_006514.2 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr2:166901576 T>C maps to NM_001165963.1 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr19:35524707 G>A maps to NM_199037.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:165948830 G>C maps to NM_006922.3 L1580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr17:62043902 C>T maps to NM_000334.4 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr7:29963704 G>A maps to NM_001145514.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr22:43606073 G>A maps to NM_173050.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr7:4259753 G>T maps to NM_152744.3 V1851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:4026874 C>T maps to NM_152744.3 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr17:71410869 G>A maps to NM_001144952.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr2:192711354 C>T maps to NM_004657.5 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr14:24912007 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr12:113830760 A>G maps to NM_006843.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr18:56816767 C>T maps to NM_033280.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr17:75190802 A>G maps to NM_001039573.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr17:75208129 G>A maps to NM_001039573.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr1:177936855 G>A maps to NM_033127.2 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:39502454 G>A maps to NM_006364.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr20:18516371 G>T maps to NM_001172745.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr4:119649798 G>A maps to ENST00000379735 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr4:83742200 T>G maps to ENST00000505472 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr3:127786280 C>T maps to ENST00000464451 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr18:12955478 A>G maps to NM_001013437.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr20:13912351 T>G maps to NM_025229.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr1:169699642 C>A maps to NM_000450.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr1:151338897 G>A maps to ENST00000435071 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr3:50225346 C>T maps to NM_004186.3 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr9:91994101 C>T maps to NM_006378.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:91993633 G>A maps to NM_006378.3 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr5:115813738 G>A maps to ENST00000257414 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:48052513 T>A maps to NM_153618.1 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr17:7474040 C>T maps to ENST00000321337 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:87369112 C>A maps to NM_004261.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:118774682 C>T did not map to a codon.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr23:118771067 C>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:105280486 A>C did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:105280576 A>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr18:61570517 C>T maps to NM_001143818.1 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr18:61326674 G>A maps to NM_006919.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr18:61465876 C>A maps to NM_001040147.1 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr7:100779017 G>A maps to NM_000602.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr11:75282972 C>T maps to NM_001235.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr3:167508322 T>C maps to NM_005025.4 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr1:28598955 C>T maps to NM_031459.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr18:42531833 C>T maps to NM_015559.2 C843C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:47098399 G>A maps to NM_014159.6 Q2292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr3:47103766 G>C maps to NM_014159.6 S2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr14:99865138 G>A maps to NM_032233.2 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr12:123889486 G>A maps to NM_020382.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr3:4354790 C>T maps to NM_006515.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr3:4355171 C>G maps to NM_006515.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr17:27286488 G>A maps to NM_178860.4 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:29900011 C>T maps to NM_201575.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr19:2247980 A>C maps to NM_007165.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr1:38435136 C>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr2:198273240 A>G maps to NM_012433.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:31976292 C>A maps to NM_001007467.1 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr1:168205988 C>T maps to NM_199344.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr14:36946256 G>A maps to NM_001101341.1 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr10:81373778 G>A maps to NM_001093770.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr10:81706232 G>A maps to NM_003019.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr17:78184760 G>A maps to NM_000199.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr17:2282480 C>A maps to NM_014853.2 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:40803286 C>T maps to NM_015705.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:123480555 G>T did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:249107312 G>A maps to NM_030645.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:17747098 C>T maps to NM_003026.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr23:19764443 T>A did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:145393443 G>A maps to NM_152550.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr19:51165084 G>A did not map to a codon.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr17:7535329 T>C maps to NM_001040.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr19:4284901 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:4290593 G>A maps to NM_020209.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr15:45470423 T>C maps to ENST00000437903 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr6:146215309 T>C maps to ENST00000367503 Q1561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr6:146271525 G>A maps to ENST00000367503 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:9900278 G>C did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:9905236 G>A did not map to a codon.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr23:9900905 A>G did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:50378310 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr11:406532 A>G maps to NM_021805.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr20:3670828 G>A maps to NM_023068.3 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr11:116719847 G>A maps to ENST00000445177 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:100841630 G>A maps to ENST00000262901 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr6:100868814 G>A maps to ENST00000262901 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr6:100911317 C>T maps to ENST00000262901 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr21:38098526 G>A maps to NM_005069.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr15:75688838 T>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr19:16973237 C>T maps to NM_015260.1 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr11:65408859 G>A maps to NM_153253.29 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr14:72055665 C>T maps to NM_015556.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr1:232626741 G>A maps to NM_020808.3 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr1:232607259 C>T maps to NM_020808.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr19:38643515 T>C maps to NM_015073.1 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr20:1517873 C>T maps to ENST00000381621 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr5:54720584 C>T maps to NM_015360.4 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr8:134050854 G>A maps to NM_006748.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr1:160719611 G>A maps to NM_021181.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr2:219258871 G>A maps to NM_000578.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr5:127448570 G>A maps to NM_001046.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr16:56928467 C>T maps to NM_000339.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr16:56921898 G>A maps to NM_000339.2 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr5:1081824 C>T maps to NM_006598.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr7:122768984 C>T maps to NM_022444.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr7:122759133 C>T did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr10:91192820 T>C maps to NM_213606.3 *517W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr2:230923894 G>A maps to NM_152527.4 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr17:80195560 C>T maps to NM_001042423.1 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr6:25779394 G>A maps to NM_005495.2 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr11:22363145 C>T maps to NM_020346.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:49933844 C>T maps to NM_020309.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr21:46951524 G>T maps to NM_194255.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr19:15073100 G>A maps to NM_005071.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr8:42297082 C>T maps to NM_006749.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr11:63064781 C>T maps to NM_001039752.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr11:64360336 C>T maps to NM_144585.2 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr6:110778135 G>A maps to NM_033125.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr11:62749447 G>A maps to NM_004790.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:129498600 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr17:73282426 G>A maps to NM_021734.4 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:128651876 C>T maps to NM_031291.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr7:87466057 G>A maps to NM_018843.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr12:58014089 C>T maps to NM_133489.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr7:107314666 C>T maps to NM_000441.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:205897098 G>A maps to NM_134325.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr4:25677956 G>A maps to NM_006424.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr4:25677848 G>A maps to NM_006424.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr6:88187185 C>G maps to NM_006416.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:48763801 A>T did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr6:137245386 G>T maps to NM_001008783.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:234454540 C>T maps to NM_173508.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr7:140058507 G>A maps to NM_207113.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:79256072 C>T maps to NM_001037984.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr17:79219798 G>A maps to NM_001037984.1 Q973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:61451519 A>G maps to NM_001172702.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr8:145639356 C>G maps to NM_130849.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr17:1516557 G>A maps to ENST00000382147 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr8:142228889 G>A maps to NM_001080431.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr9:115648894 T>G maps to NM_033051.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr20:3209829 G>A maps to NM_001174090.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr4:72121037 A>C maps to NM_001098484.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr22:32498214 G>A maps to NM_000343.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:32487647 C>T maps to NM_000343.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr21:35468231 A>G maps to NM_006933.4 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr2:108604712 C>T maps to NM_021815.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr12:85255482 A>G maps to NM_182767.4 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr5:1409835 G>A maps to NM_001044.4 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr8:17409357 C>A maps to NM_001164771.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr23:70148833 C>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:70148063 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr14:23282565 C>T maps to NM_001126106.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr19:47935601 G>A maps to NM_015063.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:27440679 G>A maps to NM_003047.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr2:103281659 G>A maps to NM_003048.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr5:491956 G>A maps to NM_004174.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr16:67304912 C>T maps to NM_004594.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:135112295 G>C did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:135106544 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr23:46510651 C>T did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr12:21422505 A>G maps to NM_134431.3 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr12:21392092 T>C maps to NM_006446.4 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr12:21030808 C>T maps to NM_019844.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:21028268 T>C maps to NM_019844.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr3:133654660 G>A maps to NM_005630.2 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:61288351 G>A maps to NM_016354.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr5:101585437 C>T maps to NM_180991.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr5:101583041 C>T maps to NM_180991.4 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr5:101582954 C>A did not map to a codon.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr17:33679773 C>T maps to NM_152270.3 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr17:33738551 C>T maps to NM_018042.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr17:33738558 A>C maps to NM_018042.3 L512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr10:98797513 G>A maps to NM_003061.2 D769D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr4:20597370 C>T maps to ENST00000273739 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:20597442 C>T maps to ENST00000273739 C1115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr4:20618725 G>A maps to ENST00000273739 Q1360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr5:168093479 G>A maps to NM_003062.2 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:142717274 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:142717375 G>T did not map to a codon.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr13:88329499 A>G maps to NM_015567.1 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:128632025 C>G did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:128633715 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:56568510 G>A maps to NM_003075.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr17:38792703 C>T maps to NM_003079.4 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr22:45768072 C>A maps to NM_148674.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr22:45785705 G>A maps to NM_148674.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr22:45779409 G>A maps to NM_148674.3 C665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr2:17884528 C>T maps to ENST00000381272 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr17:18219588 G>A maps to NM_144775.2 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr2:88393053 C>G maps to NM_198274.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:88387389 G>A maps to NM_198274.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr1:153633755 C>T maps to NM_012437.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr2:96970468 C>T maps to NM_014014.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:41268828 G>A maps to NM_004596.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr20:16712311 G>C did not map to a codon.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr15:25438439 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:86237977 A>G did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr11:64803112 C>T maps to NM_013306.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:130750570 G>A maps to NM_014758.2 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr1:179320473 T>C maps to NM_003101.4 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:179310291 C>G maps to NM_003101.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr16:11349038 G>T maps to NM_003745.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr2:46985883 C>A maps to NM_144949.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr9:138590204 G>A maps to NM_001101677.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr16:598067 C>T maps to NM_005632.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr11:121429380 G>C maps to NM_003105.5 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr11:121358799 T>A maps to NM_003105.5 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr22:38379482 G>A maps to NM_006941.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:55370801 C>A maps to NM_022454.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:55370803 C>T maps to NM_022454.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:139586762 G>A did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr2:231367784 A>G maps to NM_001080391.1 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:118516182 T>C maps to NM_206996.2 E2002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr9:35811424 G>A maps to NM_001039592.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:140785690 G>T did not map to a codon.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr23:140785766 A>G did not map to a codon.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr23:140785681 G>T did not map to a codon.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr23:140785748 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:144337222 C>T did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:142795436 C>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr3:172631477 A>G maps to NM_031955.5 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr15:45713341 C>T maps to NM_024063.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:34508916 G>A maps to NM_012391.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr11:64939961 A>G maps to NM_001008778.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr5:35697830 T>C maps to NM_024867.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr16:89620235 C>T maps to NM_003119.2 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr2:228890205 G>A maps to NM_001142644.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr2:228846501 G>A maps to NM_001142644.1 Y1678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:50926143 G>A maps to NM_003121.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr2:139308481 G>A maps to NM_001001664.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr1:153085128 A>G maps to NM_001014450.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr13:80911692 G>A maps to NM_005842.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:141693968 C>T maps to NM_030964.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr9:131337004 C>T maps to NM_001130438.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr14:65258513 G>A maps to ENST00000389723 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr2:54880942 C>G maps to NM_003128.2 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:40998961 G>A did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:41063164 C>T maps to NM_020971.2 D1842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr15:42172440 A>G maps to ENST00000320955 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:45974845 C>T maps to NM_021199.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:45616591 G>A maps to NM_018079.4 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr2:45620174 C>T maps to NM_018079.4 E869E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr16:30734515 C>G maps to NM_006662.2 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr16:4242360 G>A maps to ENST00000330063 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr20:62178603 A>G maps to NM_080823.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:57340269 C>T maps to NM_006947.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr7:104782647 T>C maps to ENST00000336613 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:24995839 T>C maps to NM_005839.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr16:2820395 C>A maps to NM_016333.3 R2689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr2:170667376 C>T maps to NM_003142.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr17:27994186 G>A maps to NM_033389.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr7:149474866 G>A maps to NM_198455.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr7:149489166 G>A maps to NM_198455.2 Q1805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr7:149486392 C>T maps to NM_198455.2 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr23:48125815 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:48053621 G>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr11:130069891 C>T maps to NM_021978.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr2:107460055 C>T maps to NM_001142351.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr9:130672315 G>C maps to NM_175039.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr3:52539709 C>T maps to NM_015136.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr3:52552601 C>T maps to NM_015136.2 H1620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr12:104033986 G>A maps to NM_017564.9 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr12:104125352 G>A did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr12:104138999 C>A maps to NM_017564.9 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr12:104049283 C>T maps to NM_017564.9 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:123196966 A>T did not map to a codon.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr23:123179196 C>T did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr2:153003684 T>C maps to NM_005843.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:51858175 G>A maps to NM_139171.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr4:70866653 A>G maps to NM_003154.2 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr20:47732386 T>C maps to NM_017453.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:242437036 G>A maps to NM_006374.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr7:23871942 T>A maps to NM_031414.3 C1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr4:5461891 C>G maps to NM_018401.1 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr12:27467497 C>T maps to NM_015000.3 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr20:62272735 G>A maps to NM_015894.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:74281474 G>A maps to NM_004809.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr13:39564827 G>A maps to NM_145286.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr12:16050899 C>T maps to ENST00000025399 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr6:144508399 C>T maps to NM_003764.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:93733521 A>G maps to NM_001001850.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr10:104353822 G>T did not map to a codon.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr20:46305255 C>A maps to NM_001161841.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr4:70709894 C>T maps to NM_005420.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr19:49094918 C>A maps to NM_177973.1 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:4491009 G>A maps to NM_182760.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr7:56145815 A>T maps to ENST00000395437 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr17:73177150 C>G did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:48559032 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:67925271 G>A maps to NM_017635.3 D847D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr17:30303571 C>T maps to NM_015355.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr9:113170751 A>G maps to ENST00000374463 C2379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr9:113139602 G>C maps to ENST00000374463 R3487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr9:113275227 G>A maps to ENST00000374463 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr10:29820186 G>A maps to NM_021738.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:16774793 C>A did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr1:115401332 G>A did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr1:115401229 A>G maps to NM_003176.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr9:93606245 G>A maps to NM_003177.5 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr6:152763233 C>A maps to NM_182961.2 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr6:152783986 T>C maps to NM_182961.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr6:152651647 C>T maps to NM_182961.2 A4724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr21:34038342 G>A maps to NM_003895.3 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:33529815 A>G maps to NM_198992.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:85420399 C>T maps to ENST00000359152 A1504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:99931047 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:99956504 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:99931058 C>T did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:37969645 C>T did not map to a codon.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr22:39814842 G>A maps to NM_006116.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr10:123844063 C>T maps to NM_206862.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr23:70626501 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:70618474 G>A did not map to a codon.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr23:70621405 G>T did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:70679528 G>T did not map to a codon.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr16:84213254 G>A maps to NM_005679.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr9:32630689 A>G maps to NM_153809.2 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr10:105145229 C>T maps to NM_006951.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:77394338 C>T did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr2:160053204 T>C maps to NM_033394.2 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:27849513 C>T maps to NM_020791.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr12:118693345 T>C maps to NM_016281.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr5:33445452 A>G maps to ENST00000455217 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr1:19168268 G>A maps to NM_152232.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr1:19166819 G>T maps to NM_152232.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:19181132 G>A maps to NM_152232.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr12:11061882 C>T maps to NM_023920.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:10959420 G>A maps to NM_023918.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr16:71610261 G>A maps to NM_000353.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:153640434 A>T did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr4:38091701 C>T maps to NM_015173.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr4:26640407 C>T maps to NM_018317.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr15:74178444 C>T maps to NM_153356.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr3:99979909 C>T maps to ENST00000394144 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:48418190 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:48418953 C>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:48418055 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr17:34499226 G>A maps to NM_001001417.5 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr13:75861014 G>A maps to ENST00000431480 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:106109196 A>G did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:106083909 T>C did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr24:6911097 C>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr6:170871045 A>G maps to NM_003194.4 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr7:45148518 C>T maps to ENST00000404564 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr22:19751680 C>T maps to NM_080647.1 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr6:85448224 A>T maps to NM_001080508.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr23:79279562 C>T did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr12:114793417 G>A maps to NM_000192.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8107-01A-13D-2395-08 chr19:3600464 A>C maps to NM_201636.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr7:139529239 G>A maps to NM_001166253.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:102864216 G>A did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr8:74858990 C>T maps to NM_005648.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr18:44561500 C>T maps to NM_016427.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:44561110 T>G maps to NM_016427.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr15:57543546 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:85531437 C>T maps to NM_031283.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr11:67816586 G>T maps to NM_006019.3 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:149755649 A>G maps to ENST00000451292 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr6:170144256 C>T maps to NM_174910.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr12:104374740 G>T did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr14:90455298 C>T maps to NM_018319.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:46655894 G>A maps to NM_001010870.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr6:46656281 C>T maps to NM_001010870.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr11:12901385 G>A maps to NM_021961.5 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:35445109 C>T maps to ENST00000357281 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr12:3129911 C>T maps to NM_003213.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr22:41783619 A>G maps to ENST00000417325 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr22:41791867 C>T maps to ENST00000417325 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr5:1264586 G>A maps to NM_198253.2 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr10:70451204 C>T maps to NM_030625.2 H2015H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr2:74300736 C>T maps to ENST00000409262 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:70073156 C>A did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr23:104464685 G>T did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr8:30694847 T>G maps to NM_031271.3 I2601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr6:50811002 C>G maps to ENST00000263046 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr6:50683277 G>T maps to NM_172238.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr2:121991691 G>A maps to NM_014553.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr2:122005805 G>A maps to NM_014553.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr23:132351779 C>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:132351925 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:48887869 G>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:115590970 G>A maps to NM_012252.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr2:188332561 G>A maps to NM_006287.4 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr8:133912510 G>A maps to NM_003235.4 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:89177200 T>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:89177101 C>T did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr15:43545092 C>T maps to NM_201631.3 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr15:43574757 G>A maps to NM_052955.2 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr16:67876786 G>A maps to NM_020457.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr15:39883402 A>G maps to NM_003246.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr15:39882076 G>A maps to NM_003246.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr15:39884879 C>T maps to NM_003246.2 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr6:128135073 G>A maps to NM_001164685.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr6:128134186 T>C maps to NM_001164685.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:122747328 G>C did not map to a codon.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr23:122758004 C>T did not map to a codon.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr15:72040863 G>A maps to NM_024817.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr15:71535119 C>T maps to NM_024817.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr2:137814592 G>A maps to ENST00000272643 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:43779638 G>A maps to NM_005424.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr5:134785347 C>T maps to NM_001099221.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:149375644 G>T maps to NM_030953.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr3:114026860 A>G maps to ENST00000481065 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr3:114014404 C>G maps to ENST00000481065 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr17:76851868 C>T maps to NM_003255.4 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr6:54173455 T>C maps to NM_014464.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr6:54254704 G>A maps to NM_014464.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr15:30001003 G>A maps to NM_003257.3 R1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:30003071 C>T maps to NM_003257.3 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr10:98129890 G>A maps to NM_012465.3 Y948Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr15:63127958 T>C maps to NM_015059.2 A2384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:63032968 G>A did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr4:38799738 C>T maps to NM_003263.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr4:38799738 C>T maps to NM_003263.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr9:120475557 C>A maps to NM_138554.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr9:120475608 A>G maps to NM_138554.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:12906719 C>T did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:12904192 G>C did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:12938643 C>T did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr20:30723917 A>G maps to NM_014742.3 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:76109645 C>T maps to NM_007267.6 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr17:76130032 G>A maps to NM_152468.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr3:129389498 T>C maps to NM_001017395.3 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr12:94975588 G>A maps to NM_020698.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:140021556 G>A maps to ENST00000252100 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr2:98377069 G>A maps to NM_015348.1 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:98388788 C>T maps to NM_015348.1 K1473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:60703700 A>T maps to NM_017870.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:129566504 G>A maps to NM_133448.2 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:152058573 A>G maps to NM_001123228.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:109416565 A>C did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr2:62729686 T>C did not map to a codon.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr16:75481521 T>G maps to NM_145254.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:150500856 C>A maps to NM_018487.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr10:104233396 C>T maps to NM_024789.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:153247935 G>C did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr20:48700713 T>C maps to NM_199203.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr12:72091159 C>T maps to NM_018279.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:15682842 G>C did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr3:12779641 T>G maps to ENST00000431022 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:34648525 G>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr6:44116116 C>T maps to NM_018426.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr8:94828613 C>T maps to NM_153704.5 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr8:56663636 G>A maps to ENST00000434581 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr8:133764098 G>A maps to ENST00000395406 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr15:34517775 C>G maps to NM_016454.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:18723159 G>A maps to NM_153347.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr16:427458 G>A maps to NM_021259.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr17:38991039 T>A maps to NM_001195386.1 L91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr21:42845268 G>A maps to NM_001135099.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr22:37462867 G>A maps to ENST00000381792 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr22:37471259 G>A maps to ENST00000381792 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr13:101294548 C>T maps to NM_032813.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr11:57480128 G>A maps to NM_015959.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:117849481 G>A maps to NM_002160.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr6:138201286 C>T maps to NM_006290.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr18:60052047 C>T maps to NM_003839.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr8:119945443 G>A maps to NM_002546.3 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr12:6438609 C>T maps to NM_001065.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr8:9588458 C>T maps to NM_003747.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr1:175046808 C>A maps to NM_022093.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr1:175048763 C>T maps to NM_022093.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr1:201384345 G>A maps to ENST00000367312 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr16:24802980 A>C maps to NM_014494.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:24802266 T>C maps to NM_014494.2 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr16:24788378 C>T maps to NM_014494.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr17:76094487 G>T maps to NM_001142640.1 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr7:47407971 G>A maps to NM_022748.11 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr6:32018081 G>A maps to ENST00000375244 A3044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr22:22322989 C>A did not map to a codon.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:179819994 G>A maps to NM_145034.4 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr17:7577142 C>T maps to NM_001126112.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr17:7579405 G>C maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr17:7574034 T>G did not map to a codon.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr17:7579362 A>C maps to NM_001126112.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr17:7579310 C>G did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr17:7574033 C>G did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:7574011 C>A maps to NM_001126112.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:7577156 T>G did not map to a codon.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr17:7578290 T>C did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr15:43714317 C>A maps to NM_001141980.1 E1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr6:83075655 G>A maps to NM_006670.4 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr15:63354773 G>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr13:103287940 G>A maps to ENST00000376052 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr16:1291160 C>T maps to ENST00000461509 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:1292147 C>T maps to ENST00000461509 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr22:26937281 G>A maps to NM_003595.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr21:10970031 G>A maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr21:10906910 G>A maps to NM_199261.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr20:30388771 G>C did not map to a codon.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr9:139815578 C>T maps to ENST00000359662 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr3:36875228 A>G maps to NM_014831.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:123687318 G>A maps to NM_006073.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr6:41165997 G>A maps to ENST00000373108 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr3:129695935 C>T maps to NM_007117.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr12:72893327 C>T maps to NM_013381.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr8:110100139 C>G maps to NM_003301.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr13:50586069 G>A did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr8:27145294 C>T maps to NM_171982.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr3:140401984 C>T maps to NM_152616.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr11:55035823 A>G did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr4:165962268 C>T maps to NM_152620.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr15:45050859 T>C maps to NM_182985.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr3:32932669 C>T maps to NM_001039111.1 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr14:51446209 T>C maps to ENST00000338969 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:189065195 G>A maps to NM_178556.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr2:230668910 G>A maps to ENST00000389044 R868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr15:64716293 A>T maps to NM_016213.4 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr7:100465833 G>A maps to NM_003302.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:54957390 A>T did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:54955788 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:54953050 C>T did not map to a codon.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr8:72969168 G>A maps to NM_007332.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:111024434 C>T did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr11:101323745 A>G maps to NM_004621.5 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr21:45774547 G>A maps to ENST00000397932 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr9:77435279 A>G maps to NM_017662.4 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:77435240 C>T maps to NM_017662.4 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:77390826 G>A maps to NM_017662.4 H1125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr17:16321162 C>T maps to NM_016113.4 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr17:16336964 C>T maps to NM_016113.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr17:3458039 G>A maps to ENST00000381913 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr12:110234443 G>A maps to NM_021625.4 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr7:142609710 G>A maps to NM_019841.4 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr7:142573226 T>C maps to NM_018646.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr7:98576478 C>T maps to ENST00000359863 C2855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr7:100064707 C>A maps to NM_030935.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr7:100064671 G>T maps to NM_030935.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:18503251 G>A maps to NM_006292.2 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:72999932 G>A maps to NM_005786.4 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr19:50249905 G>A maps to NM_021733.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:50265269 C>T maps to NM_021733.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr8:143427184 G>A maps to ENST00000445818 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:71258151 G>A maps to NM_012339.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6691-01A-11D-1893-08 chr19:11417341 G>A maps to NM_012466.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr11:44948235 G>C maps to ENST00000425677 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:54470610 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:19625702 C>T maps to NM_032037.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:43251408 G>A maps to NM_032538.1 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr11:113233184 G>A maps to NM_017868.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr14:76241855 A>G maps to NM_015072.4 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr1:84356050 T>C maps to NM_024686.4 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr2:179645980 C>T maps to NM_133378.4 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr2:179422825 A>G maps to NM_133378.4 L26517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr2:179495025 C>T maps to NM_133378.4 T12173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr2:179456088 G>A maps to NM_133378.4 T17553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:179396155 A>G maps to NM_133378.4 Y32494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr2:179498030 C>T maps to NM_133378.4 K11755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr2:179434376 G>A maps to NM_133378.4 D22926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr2:179417787 G>A maps to NM_133378.4 R27379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:179455635 C>T maps to NM_133378.4 P17704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:179463963 G>A maps to NM_133378.4 G16284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:179431331 A>G maps to NM_133378.4 G23941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:179577500 G>T maps to NM_133378.4 S7840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr2:179413637 G>A maps to NM_133378.4 G28337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr2:179579893 G>A maps to NM_133378.4 H7429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr2:179453925 A>G maps to NM_133378.4 Y18274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr2:179430062 A>T maps to NM_133378.4 A24364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr2:179456395 T>C maps to NM_133378.4 V17482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr2:179410160 A>G maps to NM_133378.4 S29324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr17:72246148 C>T maps to NM_032646.5 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr17:72233512 C>T maps to NM_032646.5 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr17:72249348 G>A maps to NM_032646.5 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr7:2696108 C>G maps to NM_025250.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr13:19752463 C>T maps to NM_006001.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr20:57597952 C>T maps to NM_030773.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:40766566 G>A maps to NM_001070.4 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr13:113181322 A>C maps to NM_006322.4 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr22:50658941 G>C maps to NM_020461.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr6:35474050 C>T maps to NM_003322.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr6:158850781 G>A maps to NM_020245.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr4:48114403 A>G maps to NM_003328.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr22:36872904 T>A did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr14:52922040 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:72281139 G>A maps to NM_001145440.1 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:70991906 C>T maps to NM_018003.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr1:162557441 C>T maps to ENST00000367925 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr19:34929584 G>A maps to NM_005499.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr21:43833167 G>A maps to NM_018961.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr17:21731351 C>A did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr17:21730996 A>G did not map to a codon.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr6:29523935 G>T maps to NM_006398.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr5:133725923 G>T maps to NM_003337.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr11:118239406 C>T maps to NM_004788.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr15:74751067 A>G maps to NM_201265.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:4927425 G>A maps to NM_016936.3 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:19510669 C>T did not map to a codon.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr8:103359283 T>C maps to NM_015902.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr8:103266679 G>A maps to NM_015902.4 P2750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr2:27530454 C>T maps to NM_003353.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr11:73714924 G>A maps to NM_003356.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:100486856 C>T maps to NM_001015072.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr13:96489362 G>A maps to NM_020121.3 Q1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr13:96592231 A>G maps to NM_020121.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr2:234602345 C>T maps to NM_001072.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr2:234590756 C>T maps to NM_019077.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr4:69879782 C>T maps to ENST00000381096 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr4:69870720 A>G maps to ENST00000381096 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr4:70080095 G>A maps to NM_001073.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:69434169 C>T maps to NM_001076.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr6:34827129 G>A maps to NM_017754.3 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr12:100502163 C>T maps to NM_015054.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr21:43519135 C>T maps to NM_173568.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:17743589 C>T did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr15:54306801 C>T maps to ENST00000260323 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr17:33475299 G>A maps to NM_173167.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr17:33482400 C>T maps to NM_173167.2 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr6:41002807 G>A maps to NM_173561.2 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr8:35583682 C>T maps to ENST00000416672 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:35406822 C>T maps to ENST00000416672 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr6:167717404 A>G did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:167728855 C>T maps to NM_018974.3 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:74519577 A>G did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr1:216251646 G>A maps to ENST00000366943 Q1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr1:216496988 A>C maps to ENST00000366943 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr1:215914868 T>C maps to ENST00000366943 G3853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr1:216062130 G>A maps to ENST00000366943 L2620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:47101044 G>A did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:47104793 G>A did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr23:47092454 G>A did not map to a codon.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:47101901 C>T did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr13:27680003 C>T maps to NM_182488.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr18:202879 C>T maps to NM_005151.3 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:62715344 T>C maps to ENST00000280377 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr21:30419418 T>C maps to NM_006447.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr1:55638163 C>T maps to NM_015306.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr21:17250116 A>G maps to ENST00000285681 K966K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:132159578 T>C did not map to a codon.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr12:109519736 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:58259032 C>T maps to NM_032582.3 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr2:61468709 C>T maps to NM_014709.3 S2254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr2:234408534 A>G maps to NM_018218.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr12:95914958 G>A maps to NM_032147.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:55514657 A>G did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:55514134 G>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr17:5072169 C>T maps to NM_004505.2 R1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr16:9000423 C>T maps to NM_003470.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr15:50769065 G>C maps to NM_005154.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:41084137 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:41075259 G>A did not map to a codon.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr23:41057787 T>C did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr6:149340327 A>G maps to NM_005715.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr13:52605153 C>G maps to NM_021645.5 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr6:145149991 G>C did not map to a codon.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr24:15410958 A>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr24:15522900 A>G did not map to a codon.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:31747884 G>A maps to NM_006295.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr9:136641199 C>T maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:101198154 A>G maps to NM_001078.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr23:8434345 G>A did not map to a codon.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr10:76980617 G>A maps to NM_001184783.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr3:156978934 G>A maps to NM_001167912.1 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr3:87018079 A>G maps to NM_016206.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr3:10191621 C>T maps to NM_000551.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr1:156268965 C>T maps to NM_001004319.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr2:219295518 C>T maps to NM_007127.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr2:37035631 C>T maps to NM_053276.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:2648301 G>A maps to NM_003383.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr1:12461734 T>C maps to NM_015378.2 F3953F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr15:41193148 C>T maps to NM_020857.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr17:40926664 A>G maps to NM_032353.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:38796518 G>A maps to NM_014396.3 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr6:33235063 G>A maps to NM_022553.4 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr1:151158054 C>T maps to ENST00000354473 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr2:58311263 A>G maps to NM_001130480.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr23:107310284 T>C did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:107316039 C>T did not map to a codon.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr23:65247364 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:65253351 C>T did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:65253474 G>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:65253438 A>G did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr20:25057043 A>C maps to NM_014588.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:1374626 G>A maps to NM_022834.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr2:98928737 C>T maps to NM_144992.4 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr2:98744703 T>C maps to NM_144992.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr7:49842317 C>T maps to NM_198570.3 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:48542339 A>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:48545244 A>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:70597850 C>T maps to NM_022479.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:73280002 C>T maps to NM_182504.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:10077031 G>A maps to NM_017491.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr19:991973 C>T maps to NM_024100.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr23:117527111 G>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr2:74652339 G>A maps to NM_032118.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr12:122399966 C>T maps to NM_144668.4 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr18:54446753 C>T maps to NM_015285.2 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr18:54424325 G>A maps to NM_015285.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr2:190313122 T>C maps to NM_032168.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr17:1637325 C>T maps to NM_001163809.1 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr20:44237303 G>A maps to NM_147198.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr4:6304059 C>T maps to NM_006005.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr12:65460501 G>A maps to NM_007191.4 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr8:134225312 C>T maps to NM_003882.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr20:43344045 G>A maps to NM_003881.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr9:96018612 C>T maps to ENST00000297954 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr23:54335535 C>A did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr7:116937825 G>A maps to NM_003391.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr17:44845703 G>A maps to NM_030753.3 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr8:30938763 G>A maps to NM_000553.4 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:10106878 G>A did not map to a codon.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr23:10085415 G>T did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:10085534 C>T did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:10090692 G>T did not map to a codon.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr8:87443689 A>C maps to NM_007013.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr2:31588393 G>A maps to NM_000379.3 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:2729412 C>G did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:123020095 G>C did not map to a codon.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr23:123034426 A>G did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:37587095 T>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:37553612 G>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:100169557 T>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr9:100459508 G>A maps to NM_000380.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr23:128879231 A>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:64811870 G>A maps to NM_007235.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr2:216983867 T>C maps to NM_021141.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr3:142136034 C>T maps to NM_019001.3 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr20:21328890 G>A maps to NM_012255.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr1:54354657 T>G did not map to a codon.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr2:135745372 G>A maps to NM_025052.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr4:69189858 G>A maps to NM_001031732.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:21875532 T>C did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:100377161 C>T maps to ENST00000349350 R2137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:166960402 G>T maps to ENST00000307529 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:2407264 T>A did not map to a codon.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr23:2406763 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr3:101373566 G>A maps to NM_014415.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr3:114069361 G>A maps to NM_001164342.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr3:114070288 C>T maps to NM_001164342.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr3:114070215 G>A maps to NM_001164342.1 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:22852747 G>A maps to NM_014870.3 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr4:4304567 G>A maps to NM_145291.3 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr6:33423521 G>A maps to NM_152735.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:64721963 C>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:64719803 G>T did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:64721754 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr13:46619597 A>G maps to ENST00000242848 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr19:47575122 G>A maps to NM_015168.1 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr19:47593320 G>A maps to NM_015168.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr19:47570839 G>A maps to NM_015168.1 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr2:113089665 A>G maps to NM_198581.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:64139084 C>A did not map to a codon.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr1:52889612 C>T maps to NM_001009881.2 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:117960228 G>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr4:25351254 C>T maps to NM_024936.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:77912923 G>T did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:77913194 A>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:88967853 G>A maps to NM_024617.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:80604489 C>T maps to NM_032280.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr2:207169635 G>A maps to NM_020923.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr6:158066843 C>T maps to NM_024630.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr3:113677374 C>T maps to NM_173570.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr7:6624734 C>T maps to NM_018106.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr2:145147368 T>C maps to NM_014795.3 K1098K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr9:74970964 G>A maps to ENST00000437241 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr8:135649704 T>C maps to NM_020863.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr16:72821212 C>A maps to NM_006885.3 S3654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr16:72991938 G>C maps to NM_006885.3 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr9:115811699 T>C maps to NM_003408.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:144332525 C>T maps to NM_173832.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr20:50701275 G>A maps to NM_199427.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr23:24229262 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:2306941 C>T maps to NM_020972.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr13:100637725 G>T maps to NM_007129.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr3:147108851 G>C maps to NM_001168379.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr7:99631510 T>C maps to NM_003439.1 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr16:25251835 G>A maps to NM_001012981.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr3:178748787 C>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr7:44799775 C>T maps to NM_031449.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr13:20656934 C>T maps to NM_001190965.1 R1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr23:70463797 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:70464670 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:70464209 C>A did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr10:285430 A>G maps to NM_006624.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:9522710 C>T maps to NM_003442.5 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:47272248 A>C did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:47269680 G>A did not map to a codon.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr6:28053479 C>T maps to NM_003447.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:47836605 C>T did not map to a codon.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr23:152083047 T>C did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr3:44683422 G>A maps to NM_006991.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:3282874 C>T maps to NM_198088.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr11:123601197 C>A maps to NM_003455.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:123596989 C>T maps to NM_003455.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:3169668 C>T maps to NM_001042428.1 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr17:30696690 G>A maps to ENST00000394679 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr19:22155222 T>C maps to NM_007153.3 K871K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr19:58453809 T>C maps to NM_005773.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr19:37005408 T>C maps to NM_001166038.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:152612568 G>A did not map to a codon.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr22:22869693 C>T maps to NM_080740.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:22843525 C>T maps to NM_080764.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:129354411 A>G did not map to a codon.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr21:43411482 G>A maps to NM_020727.4 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr16:58030900 C>T maps to NM_020807.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr10:43089023 T>C maps to NM_006955.1 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr10:43089128 G>A maps to NM_006955.1 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr10:43088768 A>G maps to NM_006955.1 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr19:53652554 G>A maps to NM_001172674.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:47308565 G>T did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:47307605 T>G did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:47315319 C>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:47307145 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:58084869 C>T maps to NM_017879.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr19:21216299 T>C maps to NM_025189.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:11890885 G>T maps to NM_152355.2 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr3:44496822 C>T maps to NM_181489.5 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr6:57012700 G>A maps to NM_001031623.2 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr9:109689382 C>T maps to NM_021224.4 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr19:11917409 G>A maps to NM_152356.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr19:22817126 T>G did not map to a codon.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr10:77159073 C>T maps to NM_032772.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr18:14106370 C>T maps to NM_145287.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr19:31038958 G>A maps to NM_014717.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:30935047 C>T maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:31040140 C>T maps to NM_014717.1 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr19:31040080 C>T maps to NM_014717.1 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:31040263 G>A maps to NM_014717.1 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr19:2852902 C>T maps to NM_152791.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:9453654 C>T maps to NM_032497.1 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:9578275 T>A maps to NM_152476.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr19:56901870 C>T did not map to a codon.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr15:85326611 C>T maps to NM_014630.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:116811426 C>T maps to ENST00000374126 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr17:16527451 C>A maps to NM_020787.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:47918327 A>C did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:47920206 C>A did not map to a codon.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr1:91405998 G>T maps to NM_201269.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:91382482 G>A maps to NM_201269.1 R1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:22291313 G>A did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:22291549 G>A did not map to a codon.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr19:22363762 G>A maps to NM_001001411.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr1:151258916 A>G maps to NM_020832.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:151261050 C>T maps to NM_020832.1 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr8:81577127 C>T maps to NM_001033723.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr19:57133635 G>A maps to NM_021216.4 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:84525046 A>G did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr7:56006945 A>C maps to NM_182633.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:80789718 G>C maps to NM_024702.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr6:35255506 C>A maps to NM_003427.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr19:53958930 C>G maps to NM_001008401.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr19:53911500 G>A maps to NM_001040185.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr15:35274298 G>C maps to NM_014106.3 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr19:12739848 G>T maps to NM_153358.2 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr19:12491948 T>C did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:47774743 T>C did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr20:57766793 C>T maps to NM_178457.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:57176020 C>T maps to NM_001005850.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:12154972 G>A maps to NM_001080404.1 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr19:22574656 T>C maps to NM_001098626.1 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr1:238048464 C>T maps to NM_021186.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr7:49977165 T>C maps to NM_007009.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:58596147 C>T maps to NM_001145542.1 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:33960424 T>G maps to NM_145238.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr19:56704395 C>T maps to NM_001080456.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr19:56704283 A>G maps to NM_001080456.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr2:187702142 G>A maps to NM_182521.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr2:187712477 C>T maps to NM_182521.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr11:113608371 C>A maps to NM_004724.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:57620230 G>A did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr17:3937517 G>A maps to NM_015113.3 N2125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:3999983 C>T maps to NM_015113.3 T561T. Only missense variants will be evaluated by CHASM.
