Sequencing variant TCGA-V4-A9F1-01A-11D-A39W-08 chr1:12711245 C>T maps to NM_001013630.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:2347525 G>A maps to NM_001089.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EQ-01A-11D-A39W-08 chr17:67119474 A>G maps to NM_080284.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:1054603 C>T maps to NM_019112.3 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8O-01A-11D-A39W-08 chr17:960238 G>A maps to NM_021962.2 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr17:73942870 G>A maps to NM_004035.6 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8Q-01A-11D-A39W-08 chr1:2939191 G>A maps to NM_080431.4 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr12:52309168 G>A maps to NM_001077401.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr14:70925883 T>C maps to NM_003813.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr5:33576197 G>A maps to NM_030955.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr3:123049782 G>A maps to NM_183357.2 H533H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:4164054 G>A maps to NM_001116.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:135778797 G>A maps to NM_017651.4 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr3:105253507 G>C maps to NM_001627.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ET-01A-11D-A39W-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr11:111715341 G>A maps to ENST00000428306 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:73828484 C>T maps to NM_015120.4 D4011D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr17:4536774 T>A maps to NM_001140.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F1-01A-11D-A39W-08 chr2:233323456 C>T maps to NM_001631.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr11:118071313 C>T maps to NM_001098526.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A888-01A-11D-A39W-08 chr14:77273136 G>A maps to NM_015305.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K8-01A-11D-A39W-08 chr11:113270062 G>T maps to NM_178510.1 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:99343421 C>T maps to NM_020349.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:201478595 G>A maps to NM_001159.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr23:55033294 C>A did not map to a codon.
Sequencing variant TCGA-RZ-AB0B-01A-11D-A39W-08 chr2:68753322 A>T maps to NM_173545.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-VD-A8KO-01A-11D-A39W-08 chr11:72408530 C>T maps to NM_001040118.2 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr23:153175797 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9F5-01A-11D-A39W-08 chr17:79827105 G>A maps to NM_004309.4 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:156907250 C>T maps to NM_198236.1 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:8221892 C>T maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr11:73073582 G>A maps to NM_014786.3 A1600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:100808009 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:100912018 C>T did not map to a codon.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr23:2825570 A>G did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:3002383 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:15306029 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:1546803 G>A did not map to a codon.
Sequencing variant TCGA-VD-AA8O-01A-11D-A39W-08 chr1:197111536 C>T maps to NM_018136.4 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr2:175945424 G>A maps to NM_001880.2 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:47538909 C>T maps to NM_020453.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr23:119513466 T>C did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:84482209 C>T maps to ENST00000416219 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr6:16327257 G>C maps to NM_000332.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr21:11058347 C>A did not map to a codon.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-V4-A9EF-01A-21D-A39W-08 chr3:52440382 G>C maps to NM_004656.2 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EU-01A-11D-A39W-08 chr3:52437839 G>A maps to NM_004656.2 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr3:52443573 G>A maps to NM_004656.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F1-01A-11D-A39W-08 chr3:52443592 G>C maps to NM_004656.2 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr6:80816424 G>C maps to NM_183050.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ES-01A-11D-A39W-08 chr23:39932446 C>G did not map to a codon.
Sequencing variant TCGA-V4-A9F3-01A-11D-A39W-08 chr20:36954746 C>G maps to NM_001725.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr22:50216675 T>C maps to ENST00000342989 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:15364969 G>A maps to NM_058243.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:111413370 C>T maps to NM_004336.3 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr7:16722415 A>G maps to NM_014038.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EU-01A-11D-A39W-08 chr14:52471210 A>C maps to NM_016039.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KO-01A-11D-A39W-08 chr15:39544395 G>A maps to NM_207445.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RZ-AB0B-01A-11D-A39W-08 chr15:73852149 G>T maps to NM_001042367.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr16:19621673 A>C maps to NM_020314.5 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZX-01A-11D-A39W-08 chr17:71239110 C>G maps to NM_017941.4 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr1:2125232 G>A maps to ENST00000359030 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr20:20177278 C>T maps to ENST00000389655 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr2:27804436 T>A maps to NM_032266.3 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr5:134782378 C>T maps to NM_130848.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr8:144124603 G>A maps to NM_173687.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr8:86389347 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9E7-01A-11D-A39W-08 chr1:159170597 C>T maps to NM_021189.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A880-01A-11D-A39W-08 chr7:134620491 C>T maps to NM_033138.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:7730999 G>A maps to NM_015215.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:119144697 G>A maps to NM_005188.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K7-01B-11D-A39W-08 chr7:23651026 C>T maps to NM_138771.3 H31H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr20:23065701 G>A maps to NM_012072.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:45258966 G>A maps to NM_001114091.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:54610385 G>A maps to NM_201546.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8Q-01A-11D-A39W-08 chr14:23522739 G>A maps to NM_022478.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:68732182 G>A maps to NM_001793.4 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:73999370 C>T maps to NM_001258.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ES-01A-11D-A39W-08 chr23:18606257 C>A did not map to a codon.
Sequencing variant TCGA-WC-A881-01A-12D-A39W-08 chr1:109803787 G>A maps to NM_001408.2 E1361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KL-01A-11D-A39W-08 chr23:100357391 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9ED-01A-11D-A39W-08 chr11:117267962 G>A maps to NM_014956.4 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr11:117222646 G>A maps to NM_014956.4 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KA-01B-11D-A39W-08 chr3:134278126 C>A maps to NM_025180.3 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:47485873 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr10:50863167 C>T maps to NM_020549.4 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr22:24108201 G>A maps to ENST00000401675 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr5:98239546 C>T maps to NM_001270.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EY-01A-11D-A39W-08 chr1:6214771 C>T maps to NM_015557.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:203194834 G>A maps to NM_003465.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:125805353 G>A maps to NM_015892.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E9-01A-11D-A39W-08 chr18:24496801 G>A maps to NM_031422.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:86959979 G>A maps to NM_001285.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr23:49845341 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr23:106171759 G>C did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:74452058 C>T maps to NM_001011880.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:150908175 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr1:246823586 A>G maps to NM_152609.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:41421731 C>T maps to NM_001843.2 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZX-01A-11D-A39W-08 chr11:100179203 T>C did not map to a codon.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr7:51095951 T>C maps to ENST00000395542 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr21:46930114 G>A maps to ENST00000359759 Q1626Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr13:110804775 C>T maps to NM_001845.4 A1611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:137697059 G>A maps to NM_000093.3 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:70809397 G>A maps to NM_016468.5 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr7:29103843 C>A maps to NM_031311.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr1:207850746 C>T maps to NM_175710.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:1413314 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:38173106 C>T maps to NM_000759.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K8-01A-11D-A39W-08 chr8:3263678 C>T maps to NM_033225.5 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr8:3263582 G>A maps to NM_033225.5 N744N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:34090145 G>A maps to ENST00000373381 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E9-01A-11D-A39W-08 chr8:113702196 A>T maps to NM_198123.1 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr1:112999730 T>C maps to NM_018704.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr17:36971160 A>T maps to NM_017748.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:61514899 G>A maps to NM_001915.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F5-01A-11D-A39W-08 chr15:22926016 T>A maps to NM_014608.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:6205174 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:34093292 G>A maps to NM_015397.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr1:32677691 G>A maps to NM_001099434.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:74596483 C>T maps to NM_004082.4 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:74593735 C>T maps to NM_004082.4 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A881-01A-12D-A39W-08 chr13:114115431 C>T maps to NM_001014283.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A888-01A-11D-A39W-08 chr1:162737091 C>T maps to NM_006182.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr24:15028512 C>A did not map to a codon.
Sequencing variant TCGA-V4-A9EU-01A-11D-A39W-08 chr12:132624743 C>T maps to NM_175066.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr23:50213355 C>G did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:12790676 C>T maps to NM_001930.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr17:21092102 C>T maps to NM_015510.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr10:12160870 G>A maps to NM_018706.5 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F4-01A-11D-A39W-08 chr19:47882983 C>T maps to NM_014681.5 S908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr6:170594479 G>T maps to NM_005618.3 C298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:46976848 G>A maps to NM_147192.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr5:118469694 C>T maps to NM_005509.4 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EH-01A-11D-A39W-08 chr17:76570917 G>T maps to ENST00000389840 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:76421568 C>T maps to ENST00000389840 T4356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EK-01A-11D-A39W-08 chr9:131008683 G>A maps to ENST00000372923 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:225688295 G>A maps to NM_014689.2 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F4-01A-11D-A39W-08 chr6:30919894 C>G maps to NM_080870.3 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:73137975 G>A maps to NM_012074.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:134008388 G>A maps to NM_006426.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr21:42064865 A>T maps to NM_001389.3 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr18:32459683 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:74002107 G>A maps to NM_003584.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr2:172600666 T>C maps to NM_001378.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr2:71755449 C>T maps to NM_001130987.1 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr2:71797030 G>A maps to NM_001130987.1 Q982Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr1:23857135 C>T maps to NM_004091.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:77417850 G>A maps to NM_203394.2 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RZ-AB0B-01A-11D-A39W-08 chr20:33722606 C>T maps to NM_018217.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr6:52319005 C>T maps to NM_018100.3 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr15:82517552 G>A maps to NM_024580.5 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:110882145 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:64622811 C>T maps to NM_006795.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr23:20152121 A>T did not map to a codon.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr23:20156730 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9EY-01A-11D-A39W-08 chr23:20156734 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr23:20156712 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr23:20156731 C>G did not map to a codon.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr23:20156739 C>T did not map to a codon.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr23:20156712 C>T did not map to a codon.
Sequencing variant TCGA-WC-A880-01A-11D-A39W-08 chr23:20156739 C>T did not map to a codon.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr23:20156734 C>G did not map to a codon.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr3:183856018 C>T maps to NM_003907.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:7213112 C>T maps to NM_001143760.1 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:141461344 G>A maps to NM_153702.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr22:29621188 G>T maps to NM_133455.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8O-01A-11D-A39W-08 chr19:45855904 C>T maps to NM_000400.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:71427098 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9ED-01A-11D-A39W-08 chr11:128360369 G>A maps to NM_001143820.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr22:29674049 C>G maps to NM_013986.3 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr15:41501728 T>C maps to NM_152596.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F5-01A-11D-A39W-08 chr14:57676362 T>C maps to ENST00000340918 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr8:118819559 G>A maps to NM_000127.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A882-01A-11D-A39W-08 chr1:169519911 A>C maps to ENST00000367796 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:134166517 C>T did not map to a codon.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr4:159076822 A>G maps to NM_001128424.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr23:34148576 T>C did not map to a codon.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr15:59144133 T>A maps to NM_001040450.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EF-01A-21D-A39W-08 chr5:94764366 G>A maps to NM_152548.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr16:89831390 G>C maps to NM_000135.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr16:89882377 C>T maps to NM_000135.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EH-01A-11D-A39W-08 chr3:10140561 T>C maps to NM_033084.3 S1448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr5:7859574 T>C maps to NM_024091.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KO-01A-11D-A39W-08 chr3:13672940 C>T maps to NM_001165035.1 N1066N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr7:102669189 C>T maps to NM_145032.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr15:91433096 T>G maps to NM_002005.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F3-01A-11D-A39W-08 chr5:170863116 C>T maps to NM_003862.2 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ES-01A-11D-A39W-08 chr15:49776571 A>C maps to NM_002009.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr10:123298225 G>A maps to ENST00000351936 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr7:33028244 G>A maps to NM_007270.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr1:152328446 G>A maps to NM_001014342.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87T-01A-11D-A39W-08 chr23:153596437 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr23:131212667 T>C did not map to a codon.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr2:49381415 A>G maps to NM_000145.3 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EK-01A-11D-A39W-08 chr23:31089833 G>T did not map to a codon.
Sequencing variant TCGA-V4-A9E7-01A-11D-A39W-08 chr16:70500084 C>T maps to NM_145059.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:7499189 G>A maps to NM_004860.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr23:153761235 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EF-01A-21D-A39W-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9A-01A-11D-A39W-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr23:153908519 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr9:101304172 G>A maps to NM_005458.7 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr23:151131075 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr23:49355850 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:230391057 G>A maps to NM_004481.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr20:42907912 C>T maps to NM_024034.3 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:27903360 G>A maps to NM_001085454.1 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:27902156 G>A maps to NM_001085454.1 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr23:100653464 T>C did not map to a codon.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr2:121748131 C>T maps to NM_005270.4 R1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RZ-AB0B-01A-11D-A39W-08 chr20:62236097 A>T maps to NM_012384.3 L76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr9:80537255 C>A maps to NM_002072.3 G48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EF-01A-21D-A39W-08 chr3:121438590 G>T maps to ENST00000393667 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:204170924 C>T maps to NM_198447.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E9-01A-11D-A39W-08 chr16:20331018 G>T maps to NM_001007240.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr17:42477395 T>C maps to NM_001002909.2 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr23:136113491 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:136112960 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9EJ-01A-11D-A39W-08 chr23:135469897 G>T did not map to a codon.
Sequencing variant TCGA-V4-A9EJ-01A-11D-A39W-08 chr14:91701319 C>T maps to ENST00000238699 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:11774454 C>T maps to NM_014668.3 N1730N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:153078527 C>T maps to NM_001114183.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr4:94693492 C>T maps to NM_001510.2 N956N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:120827587 G>A maps to NM_014619.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr5:178410054 C>T maps to NM_000843.3 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr8:30511072 G>A maps to NM_002095.4 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr4:174450362 T>A maps to NM_021973.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr15:73615895 C>T maps to NM_005477.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr11:124789906 A>G maps to NM_001037558.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr15:28441637 C>A maps to NM_004667.4 E2697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr10:94452506 C>T maps to NM_002729.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr22:19343353 C>T maps to NM_003325.3 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr21:38137354 G>A maps to NM_000411.5 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr7:27168858 A>T maps to NM_002141.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr6:44221298 C>T maps to NM_007355.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr1:161495095 T>C maps to NM_002155.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:3123052 C>T maps to NM_002111.6 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:53602624 G>A did not map to a codon.
Sequencing variant TCGA-VD-AA8M-01A-11D-A39W-08 chr16:1574690 C>T maps to NM_014714.3 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr15:65622131 G>A maps to NM_004884.3 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr1:201190722 G>T maps to NM_001164586.1 P3350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87W-01A-11D-A39W-08 chr3:118824024 T>C maps to NM_152538.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F3-01A-11D-A39W-08 chr1:159901297 G>A maps to NM_001135050.1 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr1:207073690 C>T maps to NM_001185156.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:121551526 C>T maps to NM_014937.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr5:75969312 A>G maps to NM_006633.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr12:66638725 A>G did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:52358677 C>T maps to NM_002203.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:54799458 G>A maps to NM_002205.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr7:20421426 T>C maps to NM_002214.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8S-01B-11D-A39W-08 chr3:4725408 G>A maps to ENST00000356617 W1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr12:26943117 G>A maps to NM_002223.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr6:33654820 G>A maps to ENST00000374316 E2005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:105618597 G>A maps to NM_002226.3 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr1:65339051 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr4:6050592 C>A maps to NM_001099433.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:87723888 C>T maps to NM_020655.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr23:8699906 C>A did not map to a codon.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr19:8389558 C>T maps to NM_198471.2 R746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:5154302 G>A maps to NM_002234.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:17793390 C>T maps to NM_001112741.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:68129131 C>T maps to NM_018658.1 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:78651327 G>A maps to NM_001161352.1 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:138651620 C>T maps to ENST00000298480 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EA-01A-11D-A39W-08 chr1:23377000 T>C maps to NM_001009999.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr5:137750821 G>A maps to NM_016604.3 E1067E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr23:44918344 A>G did not map to a codon.
Sequencing variant TCGA-VD-A8KL-01A-11D-A39W-08 chr7:86542376 G>A maps to NM_001142749.2 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:115421679 C>T maps to NM_133465.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KF-01A-11D-A39W-08 chr1:11983370 C>A maps to ENST00000376576 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8M-01A-11D-A39W-08 chr15:69715495 A>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:158047862 C>T maps to ENST00000368173 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr13:33638013 C>T maps to NM_004795.3 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr13:33635717 C>T maps to NM_004795.3 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr23:24007012 C>T did not map to a codon.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr10:135020363 C>T maps to ENST00000368572 S1164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:10671901 G>A maps to NM_023008.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr17:39620400 G>A maps to NM_002278.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr17:39137346 A>T maps to NM_182497.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr17:39316784 G>A maps to NM_032524.1 T53T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VD-A8KO-01A-11D-A39W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr22:41621886 C>T maps to NM_031488.4 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr16:67976290 G>A maps to NM_000229.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K9-01A-11D-A39W-08 chr1:152681847 C>T maps to NM_178356.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr5:38496649 T>C maps to NM_002310.5 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E9-01A-11D-A39W-08 chr19:55106754 T>C maps to NM_006863.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr3:197710813 G>A maps to NM_001136049.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr12:16753677 C>T maps to ENST00000441439 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr23:118109320 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:161027539 C>T maps to NM_005577.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:170060630 G>A maps to NM_004525.2 D2622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:186295494 G>A maps to ENST00000362004 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:53742397 G>A maps to NM_004631.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr2:44145164 T>C maps to NM_133259.3 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KN-01A-11D-A39W-08 chr1:54426037 G>A maps to NM_052940.3 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:131670588 C>T maps to NM_001127244.1 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8N-01A-11D-A39W-08 chr1:74507164 G>A maps to NM_001105659.1 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K9-01A-11D-A39W-08 chr7:110763685 A>G maps to NM_018334.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EJ-01A-11D-A39W-08 chr17:7760096 A>G maps to NM_032356.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:41129853 C>T maps to ENST00000308370 C1299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9A-01A-11D-A39W-08 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr19:42342288 C>T maps to NM_173506.4 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:235827916 G>A maps to NM_000081.2 G3681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87W-01A-11D-A39W-08 chr23:51640904 A>G did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:119509575 G>A maps to NM_005907.2 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87Y-01A-11D-A39W-08 chr5:109106203 C>G maps to NM_002372.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr23:43703011 T>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:43702950 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:210559485 C>T maps to NM_002374.3 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:21201791 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:20081642 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr20:43936910 G>A did not map to a codon.
Sequencing variant TCGA-VD-A8KJ-01A-11D-A39W-08 chr18:74729168 A>C maps to NM_001025101.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:21886608 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr6:100369076 C>T maps to NM_032503.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr23:70339610 C>T did not map to a codon.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr16:3293587 C>T maps to NM_000243.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A88A-01A-11D-A39W-08 chr19:42839497 C>A maps to ENST00000251268 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr5:179226504 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr11:102487571 G>C maps to NM_004771.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr23:154014530 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:19077850 C>T maps to NM_054030.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KF-01A-11D-A39W-08 chr4:84377253 C>T maps to NM_016067.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F2-01A-11D-A39W-08 chr12:27863871 C>T maps to NM_021821.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:60531220 C>T maps to NM_001098835.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr8:16012620 G>A maps to ENST00000445506 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:65857065 C>T maps to NM_001031679.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr3:9743590 C>T maps to NM_001077525.2 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr11:92703061 C>A maps to NM_005959.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EJ-01A-11D-A39W-08 chr11:1101115 C>A maps to ENST00000441003 T2505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:1360195 C>T maps to NM_032853.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr9:113449429 T>C maps to ENST00000189978 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:48597027 C>T maps to NM_032133.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr12:81101599 T>C maps to NM_002469.2 Y34Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr22:36684925 C>T maps to NM_002473.4 T1539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:101259573 C>T maps to NM_138403.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F0-01A-11D-A39W-08 chr19:8620656 C>T maps to NM_012335.3 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:171371512 C>T maps to NM_138995.3 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:76890114 C>T maps to NM_000260.3 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:76912670 G>A maps to NM_000260.3 P1677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr10:95191209 C>T maps to NM_013451.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:95119636 G>A maps to NM_013451.3 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr17:59668489 G>A maps to NM_199290.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EY-01A-11D-A39W-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr3:47041743 G>A maps to NM_015175.1 Q1385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:21809641 C>T maps to NM_032264.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87T-01A-11D-A39W-08 chr19:19349147 G>T maps to NM_004386.2 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:50188795 C>T maps to NM_001037806.3 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr20:33328467 G>A maps to NM_014071.2 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:31557651 G>A maps to NM_147130.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ET-01A-11D-A39W-08 chr7:123190628 T>A maps to NM_005000.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EQ-01A-11D-A39W-08 chr6:11213717 G>A maps to NM_006403.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87Y-01A-11D-A39W-08 chr22:29885827 C>A maps to NM_021076.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr20:50090553 G>T maps to NM_012340.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KJ-01A-11D-A39W-08 chr2:178096251 G>T maps to NM_006164.3 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr23:17744068 G>A did not map to a codon.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr5:37064955 C>T maps to NM_133433.3 R2793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr19:55494139 C>T maps to NM_017852.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:56369493 G>A maps to NM_134444.4 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:120506200 C>T maps to NM_024408.2 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8M-01A-11D-A39W-08 chr1:153658319 C>T maps to NM_000906.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:27613316 G>A maps to NM_020772.2 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr19:50412425 G>C maps to NM_012346.4 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr17:47656052 G>A maps to ENST00000513748 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:41333539 C>T did not map to a codon.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr13:53624626 A>G maps to NM_006418.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr19:46056951 G>A maps to NM_025136.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr6:154411257 C>T maps to NM_001145279.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:15918448 G>A maps to NM_013940.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr1:248224858 G>A maps to NM_001004687.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr17:3195503 G>A maps to ENST00000397187 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr15:22368715 C>T maps to NM_001004719.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr11:5968659 G>A maps to NM_001003443.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr12:55759764 A>T maps to NM_001005497.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr1:158686996 C>T maps to ENST00000368146 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr11:124440296 C>T maps to NM_001005194.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A888-01A-11D-A39W-08 chr7:141618728 C>A maps to NM_001001656.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:146058661 G>A maps to ENST00000447906 R1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZX-01A-11D-A39W-08 chr11:57118297 C>A maps to NM_002559.2 C256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr1:17395606 C>A maps to NM_007365.2 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr9:112899620 G>T maps to NM_007203.4 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:34648124 G>A maps to NM_019619.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr13:101020821 G>A maps to NM_000282.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr4:134084204 T>C maps to NM_032961.1 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:99662741 G>A did not map to a codon.
Sequencing variant TCGA-VD-A8KF-01A-11D-A39W-08 chr13:67800082 G>A maps to NM_203487.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:140237879 G>A maps to NM_018901.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr5:140174911 G>T maps to NM_018905.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:140209241 G>A maps to NM_018909.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ET-01A-11D-A39W-08 chr5:140554266 G>A maps to NM_018940.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:140754747 C>T maps to NM_018919.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ED-01A-11D-A39W-08 chr21:47845773 C>T maps to NM_006031.5 S2403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr5:58289224 G>C maps to NM_001104631.1 S330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr1:144856944 G>A maps to NM_014644.4 V2180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:55146590 C>T maps to ENST00000507166 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K8-01A-11D-A39W-08 chr8:94935039 G>A maps to NM_001161778.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:77224668 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:18944632 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr20:33169373 G>A maps to NM_080476.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr10:3191919 G>A maps to ENST00000380989 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:198948756 G>A maps to NM_006226.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:67862207 G>A maps to NM_016445.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A880-01A-11D-A39W-08 chr3:146309608 G>C maps to NM_001085420.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr9:140374844 T>C maps to NM_001098537.1 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:50917081 C>T maps to ENST00000391817 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr2:105472294 C>T maps to NM_006236.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr2:105472297 T>C maps to NM_006236.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RZ-AB0B-01A-11D-A39W-08 chr13:79175837 C>T maps to NM_006237.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A88A-01A-11D-A39W-08 chr22:46615722 C>T maps to NM_001001928.2 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr6:35393804 C>G maps to NM_006238.4 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:18775809 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr4:159638313 G>A maps to NM_005038.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:4933600 G>A maps to NM_002705.4 F1685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr8:8998588 C>T maps to NM_024607.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K9-01A-11D-A39W-08 chr11:111636063 T>C maps to NM_181699.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A881-01A-12D-A39W-08 chr6:42978204 G>C did not map to a codon.
Sequencing variant TCGA-VD-AA8N-01A-11D-A39W-08 chr8:68992729 G>T maps to NM_024870.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr1:186276305 T>C maps to NM_005807.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr14:30108043 G>A maps to NM_002742.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr1:214169913 G>A maps to NM_002763.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr1:150297350 A>G did not map to a codon.
Sequencing variant TCGA-WC-A87Y-01A-11D-A39W-08 chr11:32858270 G>A maps to NM_024081.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr8:18729315 G>T maps to ENST00000440756 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F1-01A-11D-A39W-08 chr19:43411101 G>T maps to NM_002782.3 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr9:15506611 A>T maps to NM_001128217.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:23512168 C>T maps to NM_001099780.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr6:32809922 G>A maps to NM_148919.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:99022531 C>T maps to NM_001198879.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr6:43111197 C>G maps to NM_002821.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr11:47591271 C>T maps to NM_175732.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:88945352 G>A maps to NM_007039.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr3:47454065 T>C maps to NM_015466.2 H1460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr9:112195402 G>A maps to NM_002829.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr12:71016403 C>T maps to NM_001109754.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A983-01A-11D-A39W-08 chr9:8331703 C>T maps to NM_002839.3 Q1804Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:125763822 G>A maps to NM_031307.3 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:99817743 G>A maps to NM_024070.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:119535573 G>A maps to NM_002855.4 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ET-01A-11D-A39W-08 chr10:100147056 A>G maps to NM_032709.2 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr6:163899929 T>A did not map to a codon.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr2:73316088 G>A maps to NM_015470.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KE-01A-11D-A39W-08 chr13:111176286 T>G maps to NM_017817.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr23:129318340 T>C did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr5:36257583 C>T maps to NM_001161429.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8Q-01A-11D-A39W-08 chr12:53606944 G>C maps to NM_000966.4 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KK-01A-11D-A39W-08 chr12:18237494 C>T maps to NM_024730.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:71350831 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:71349780 C>T did not map to a codon.
Sequencing variant TCGA-WC-A87Y-01A-11D-A39W-08 chr16:321226 G>A maps to NM_183337.1 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr4:3419158 G>A maps to NM_198229.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K7-01B-11D-A39W-08 chr17:30615818 C>T maps to NM_138328.2 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F3-01A-11D-A39W-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:12918310 C>T maps to NM_006397.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr17:41180480 G>T maps to NM_005440.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr13:98829457 G>A maps to NM_178861.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87W-01A-11D-A39W-08 chr17:78332108 C>T maps to NM_020914.4 V3677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr3:78700894 C>T maps to NM_002941.3 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KN-01A-11D-A39W-08 chr12:113285536 G>A maps to NM_001143854.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr5:172395505 C>G maps to NM_016093.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr11:118888180 G>C maps to NM_001028.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr23:83374914 C>G did not map to a codon.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr6:116944014 A>G maps to NM_001010892.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr17:41143306 G>A maps to NM_173079.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr19:38951203 C>T maps to NM_000540.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr19:38979905 C>T maps to NM_000540.2 D1879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr1:237791260 G>T maps to NM_001035.2 T2107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr1:237947563 G>A maps to NM_001035.2 E4184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr15:34103221 T>A maps to NM_001036.3 L3414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:3179431 C>T maps to NM_003775.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr18:76754681 C>T maps to NM_171999.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EI-01A-11D-A39W-08 chr19:1119012 C>T maps to NM_014963.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr15:75310785 C>T maps to ENST00000361900 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr3:38913707 C>T maps to ENST00000302328 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:62018496 G>A maps to NM_000334.4 Y1715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr8:144887323 A>G maps to NM_182706.3 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8N-01A-11D-A39W-08 chr17:75208189 C>T maps to NM_001039573.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:139371002 G>A maps to NM_014866.1 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:118774740 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:95080898 C>T maps to ENST00000393080 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr18:61305231 C>T maps to NM_002974.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr3:47103827 G>A maps to NM_014159.6 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EQ-01A-11D-A39W-08 chr5:145427381 C>T maps to NM_152550.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A882-01A-11D-A39W-08 chr15:45464121 G>A maps to ENST00000437903 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8M-01A-11D-A39W-08 chr17:3514062 G>A maps to NM_013276.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KL-01A-11D-A39W-08 chr23:9864552 A>G did not map to a codon.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr13:21746792 A>T maps to NM_145061.5 L44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr17:6594095 A>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:73751217 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9ET-01A-11D-A39W-08 chr2:220033408 G>C maps to NM_001144890.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:172641885 C>T maps to NM_003705.3 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr22:18072419 C>T maps to NM_031481.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr10:101370890 G>A maps to NM_031212.3 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87T-01A-11D-A39W-08 chr23:1508132 C>A did not map to a codon.
Sequencing variant TCGA-V4-A9EC-01A-11D-A39W-08 chr5:128302198 C>T maps to NM_001017372.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr9:86894187 C>A maps to NM_022127.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr9:140127060 C>T maps to NM_080877.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:150768836 C>T maps to NM_003040.3 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr12:333590 G>A maps to NM_016615.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:20676287 G>A maps to NM_004211.3 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:44463571 G>A maps to NM_201649.2 Y627Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr8:17417929 C>A maps to NM_001164771.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F4-01A-11D-A39W-08 chr5:168175311 G>A maps to NM_003062.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr23:53410064 A>G did not map to a codon.
Sequencing variant TCGA-WC-A87Y-01A-11D-A39W-08 chr2:1263146 C>T maps to NM_018968.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K8-01A-11D-A39W-08 chr3:137484270 C>G maps to NM_004189.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A888-01A-11D-A39W-08 chr17:26906801 G>A maps to NM_006461.3 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:26912881 C>T maps to NM_006461.3 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr4:88414958 C>T maps to NM_004684.4 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9ED-01A-11D-A39W-08 chr1:16259499 G>A maps to NM_015001.2 A2255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:89614492 C>T maps to NM_003119.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:9416003 G>A maps to NM_025106.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr23:48054515 C>G did not map to a codon.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr8:53030984 T>C maps to NM_014682.2 E924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr1:77334297 G>A maps to NM_030965.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KG-01A-11D-A39W-08 chr3:136141360 A>C maps to NM_005862.2 L643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:220473353 C>T maps to NM_052902.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr20:43653752 G>A maps to NM_006282.2 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr2:48809430 G>A maps to NM_172311.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KI-01A-11D-A39W-08 chr7:75625884 G>A maps to NM_016086.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr8:110590197 G>T maps to NM_001099744.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr6:152763337 G>A maps to NM_182961.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:110022031 C>T maps to NM_001040709.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:155838011 C>T maps to NM_152280.4 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:159181682 C>T maps to ENST00000297239 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr3:9831434 G>A maps to NM_006354.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr17:34173973 C>T did not map to a codon.
Sequencing variant TCGA-V4-A9F5-01A-11D-A39W-08 chr17:61498655 G>A maps to ENST00000389520 P1781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:19181078 G>A maps to NM_152232.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr22:30690060 C>T maps to ENST00000403477 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr12:114823292 G>C maps to NM_000192.3 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr10:97443173 A>G maps to ENST00000371209 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:121000771 C>T maps to NM_005422.2 N931N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V3-A9ZX-01A-11D-A39W-08 chr12:53449608 C>T maps to NM_170754.2 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KH-01A-11D-A39W-08 chr23:104463873 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9F1-01A-11D-A39W-08 chr23:132351712 T>C did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr8:133920512 C>T maps to NM_003235.4 Y1310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:2185558 G>A maps to NM_199292.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr23:122769934 G>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr15:71952897 C>T maps to NM_024817.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr15:70347576 G>A maps to NM_005078.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:60689438 G>A maps to NM_024092.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr11:62557410 C>T maps to NM_199337.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EF-01A-21D-A39W-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8O-01A-11D-A39W-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr23:100349756 C>T did not map to a codon.
Sequencing variant TCGA-YZ-A984-01A-11D-A39W-08 chr3:194346635 C>T maps to NM_001166305.1 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:129722454 G>A maps to NM_138788.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EV-01A-11D-A39W-08 chr8:56675149 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9F2-01A-11D-A39W-08 chr9:35846949 G>A maps to ENST00000360192 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:29671409 G>A maps to NM_001193451.1 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:88566444 C>T maps to NM_181783.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EX-01A-11D-A39W-08 chr12:6439097 G>A maps to NM_001065.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:2746453 C>T maps to NM_024309.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:1950365 C>T maps to ENST00000397301 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E7-01A-11D-A39W-08 chr5:72184016 C>T maps to NM_002270.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:47408604 G>A maps to NM_022748.11 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:47408250 C>T maps to NM_022748.11 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:32017059 G>A maps to ENST00000375244 T3248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:45404589 G>A did not map to a codon.
Sequencing variant TCGA-YZ-A982-01A-11D-A39W-08 chr8:95952119 C>T maps to NM_033285.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr3:189582118 C>T maps to NM_003722.4 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9A-01A-11D-A39W-08 chr12:113723745 C>G maps to NM_001143819.1 Y574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8Q-01A-11D-A39W-08 chr16:1291301 G>A maps to ENST00000461509 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KB-01A-11D-A39W-08 chr9:139820172 C>T maps to ENST00000359662 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr6:30135041 G>A maps to NM_033229.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A881-01A-12D-A39W-08 chr11:119996546 G>T maps to NM_012101.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EH-01A-11D-A39W-08 chr1:33612879 G>A maps to NM_018207.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A980-01A-11D-A39W-08 chr4:189068324 G>A maps to NM_178556.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr21:45784125 C>T maps to ENST00000397932 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr23:107018504 G>T did not map to a codon.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr6:43251678 G>A maps to NM_032538.1 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EM-01A-11D-A39W-08 chr2:179413442 A>C maps to NM_133378.4 A28402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A883-01A-12D-A39W-08 chr4:68530981 A>G maps to NM_018227.5 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr1:19492232 G>A maps to ENST00000375267 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E5-01A-11D-A39W-08 chr8:103289312 A>G maps to NM_015902.4 T2132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:132396494 C>T maps to NM_003565.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr4:96163727 C>T maps to NM_003728.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr17:9631532 G>A maps to NM_153210.3 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87U-01A-11D-A39W-08 chr6:41766668 T>G did not map to a codon.
Sequencing variant TCGA-VD-A8KD-01A-11D-A39W-08 chr17:56056600 T>C maps to NM_007146.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr6:117589487 A>C maps to NM_182645.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K9-01A-11D-A39W-08 chr1:12328814 G>A maps to NM_015378.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr1:151149200 G>A maps to ENST00000354473 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr12:6128638 G>A maps to NM_000552.3 R1315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KM-01A-11D-A39W-08 chr14:100996251 C>T maps to NM_001161476.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr14:100992226 G>A maps to NM_001161476.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F5-01A-11D-A39W-08 chr1:118477139 C>T maps to NM_006784.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EL-01A-11D-A39W-08 chr1:109553776 G>C maps to NM_001142550.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A885-01A-11D-A39W-08 chr12:122392078 A>G maps to NM_144668.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr18:54603066 T>A maps to NM_015285.2 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr7:116937891 G>A maps to NM_003391.2 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8K9-01A-11D-A39W-08 chr19:34991048 C>T maps to ENST00000270288 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F8-01A-11D-A39W-08 chr8:56015468 C>T maps to NM_052898.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EO-01A-12D-A39W-08 chr3:14200131 C>T maps to NM_004628.4 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A882-01A-11D-A39W-08 chr3:101378835 G>A maps to NM_014415.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr16:11846639 G>A maps to NM_014153.3 Q871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr18:60242301 C>T maps to NM_017742.4 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr11:57466581 G>A maps to NM_015457.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KF-01A-11D-A39W-08 chr12:72057130 G>T maps to NM_144982.4 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:72993654 G>A maps to NM_006885.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:72993165 G>A maps to NM_006885.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EW-01A-11D-A39W-08 chr15:41099957 A>G maps to NM_001077268.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr23:101159301 G>A did not map to a codon.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr23:47272124 T>C did not map to a codon.
Sequencing variant TCGA-VD-AA8Q-01A-11D-A39W-08 chr23:47836906 A>G did not map to a codon.
Sequencing variant TCGA-V3-A9ZY-01A-11D-A39W-08 chr19:44933956 G>A maps to NM_014518.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-AA9E-01A-11D-A39W-08 chr19:57868112 C>T maps to ENST00000391705 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-A8KL-01A-11D-A39W-08 chr20:32358080 G>A maps to ENST00000375200 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E8-01A-11D-A39W-08 chr5:178506833 G>A maps to NM_014594.1 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E9-01A-11D-A39W-08 chr19:11978606 G>A maps to NM_152262.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8P-01A-11D-A39W-08 chr19:58991008 G>C did not map to a codon.
Sequencing variant TCGA-VD-A8KO-01A-11D-A39W-08 chr19:57803249 G>A maps to NM_006635.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EZ-01A-11D-A39W-08 chr7:57188368 G>A maps to NM_033273.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr19:40521031 C>T maps to NM_178544.3 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9F7-01A-11D-A39W-08 chr19:55993183 C>T maps to NM_033113.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YZ-A985-01A-11D-A39W-08 chr16:30793308 G>A maps to NM_001080417.1 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9E7-01A-11D-A39W-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A884-01A-11D-A39W-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8M-01A-11D-A39W-08 chr19:53945836 T>C did not map to a codon.
Sequencing variant TCGA-VD-AA8R-01A-11D-A39W-08 chr19:40581889 A>G maps to NM_001142577.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EE-01A-11D-A39W-08 chr9:130206860 G>A maps to NM_007135.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VD-AA8T-01A-11D-A39W-08 chr19:52659255 G>C maps to NM_001102657.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WC-A87T-01A-11D-A39W-08 chr16:3140132 G>A maps to NM_032805.1 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V4-A9EJ-01A-11D-A39W-08 chr6:28093442 C>T maps to NM_025231.1 C74C. Only missense variants will be evaluated by CHASM.
