1291 NP_705833 F476L not found in SNVbox database
1490 NP_705833 N48H not found in SNVbox database
1651 NP_705833 K337R not found in SNVbox database
2233 NP_705833 W847G not found in SNVbox database
4087 NP_705833 V462I not found in SNVbox database
4120 NP_705833 K280T not found in SNVbox database
4364 NP_705833 S75P not found in SNVbox database
4470 NP_705833 Y486N not found in SNVbox database
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:52601749 G>A maps to NM_138932.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:107620979 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:107548663 C>A maps to NM_005502.3 E2106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr17:67193232 T>C maps to NM_080282.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr7:48411970 A>G maps to NM_152701.3 A3670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:48319343 T>C maps to NM_152701.3 I2851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:2354002 G>A maps to NM_001089.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:67302905 C>A maps to ENST00000392677 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:66903901 C>A maps to NM_007168.2 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:66873703 G>A maps to NM_007168.2 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:169828433 C>A maps to NM_003742.2 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:20682947 C>T maps to NM_001163941.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:74334627 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:74282174 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:74318852 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:43406362 C>T maps to NM_033450.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:48145698 T>C maps to NM_033226.2 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:48121865 C>T maps to NM_033226.2 Q1202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:17448597 G>A maps to ENST00000302539 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:17428260 G>A maps to ENST00000302539 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:22063774 G>T maps to NM_005691.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:22025632 T>C maps to NM_005691.2 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:27052889 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:179078367 C>T maps to NM_007314.3 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:136135230 C>T maps to NM_020469.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr12:109696794 A>G maps to NM_001093.3 G2126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:134127028 C>T maps to NM_014384.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:89401044 T>C maps to NM_013227.3 P1743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:27494153 C>T maps to ENST00000375888 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr4:156784846 G>A maps to NM_017419.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr23:15609872 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:15589792 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:40063733 G>A maps to ENST00000401700 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr5:80626632 G>T maps to NM_130767.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70832207 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70823529 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70832406 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:185697684 G>A maps to NM_001995.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:108902618 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:108926384 T>G did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:108911497 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:114169442 G>A maps to NM_016234.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:20682929 G>A maps to NM_052956.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:20491924 C>T maps to NM_001010845.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:20554553 G>A maps to NM_182617.3 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:229568732 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:179294469 G>T maps to NM_004301.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:66319047 C>A maps to NM_001104.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:58697163 C>A maps to NM_018477.2 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:58701268 G>T maps to NM_018477.2 *418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:104241926 A>G maps to NM_005736.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:127185897 C>T did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr2:158594951 C>T maps to NM_001111067.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr10:127724803 G>A maps to NM_003474.4 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:120437705 T>C maps to NM_021794.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:5306708 G>A maps to NM_139056.2 K1093K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:128864215 G>T maps to NM_133638.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:79058094 G>A maps to ENST00000258883 H1386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr9:18775889 T>C maps to NM_001040272.4 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:18639250 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr9:18622330 C>T maps to NM_001040272.4 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:29253885 C>T maps to ENST00000394782 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:29261311 A>G maps to ENST00000394782 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:41220035 C>G maps to NM_024876.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:167817656 G>T maps to NM_018417.4 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr5:7727299 G>A maps to NM_020546.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:7784476 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr1:202915579 C>T maps to NM_015999.3 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:73045230 G>A maps to NM_031284.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr8:26627887 G>A maps to ENST00000356368 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:87967345 C>T maps to NM_001166693.1 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:147924916 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:147924956 C>A did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:100266098 A>T maps to NM_001025108.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:100194796 G>A maps to NM_001025108.1 F995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:88768825 G>T maps to NM_133447.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:76344054 C>A maps to NM_018046.4 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:84502844 C>T maps to NM_032717.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr11:62291940 G>C maps to NM_001620.1 P3316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:62290080 T>C maps to NM_001620.1 K3936K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr14:105418190 G>A maps to NM_138420.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:105406166 T>C maps to NM_138420.2 R5207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:353940 C>T maps to NM_020731.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr23:129299533 G>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:71874718 G>A maps to NM_032797.5 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:21331226 G>A maps to NM_144704.2 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:107252908 C>T maps to NM_001142416.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:6054937 G>A maps to NM_006303.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr1:4772160 G>T maps to NM_018836.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:151671491 G>T maps to NM_005100.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr15:86225392 A>G maps to NM_006738.4 S1706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:86259070 C>T maps to NM_006738.4 T1888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:86122534 G>A maps to NM_006738.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr12:4737295 C>A maps to NM_006422.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:49958137 C>A did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:49958837 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:33292586 C>A maps to NM_004274.4 V1856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:15512056 G>A maps to NM_014371.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:91724363 A>G maps to NM_005751.4 E3202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr6:109815250 T>C maps to NM_001145128.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:109816600 A>G maps to NM_001145128.2 L1786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:109394799 C>A maps to NM_152763.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:134252968 C>T maps to ENST00000418096 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr10:5144363 T>C maps to NM_003739.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr10:5141028 A>G maps to NM_003739.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr23:55042070 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:55042055 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:49962999 C>T maps to NM_153329.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:75545818 G>A maps to NM_000689.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:101432737 G>A maps to NM_000693.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:67790204 G>A maps to NM_001161473.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:74539001 A>C maps to NM_005589.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr16:5122950 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:110978303 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:111003113 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:63894713 G>T maps to ENST00000263440 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:3727580 G>T maps to ENST00000403787 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr17:6900278 G>A maps to NM_000697.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:4534906 A>G maps to NM_001140.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:56274660 C>T maps to NM_052947.3 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:85383001 A>G maps to NM_020778.4 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:202154231 C>A maps to NM_139163.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:85680695 G>A maps to NM_006982.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr17:33521053 G>A maps to NM_152462.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:11189076 C>T maps to NM_054028.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:71472353 G>A maps to NM_016519.4 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:118068799 C>A maps to NM_001098526.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr23:112022453 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:112022528 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:10521688 C>T maps to NM_000480.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:38431441 C>T maps to NM_001635.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:25418155 T>C maps to ENST00000510092 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:858964 G>A maps to NM_015985.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:178834091 C>A maps to NM_004673.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr9:129853994 G>A maps to NM_012098.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr17:54558121 C>G maps to NM_153228.2 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:113270688 G>A maps to NM_178510.1 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr16:89351377 C>A maps to NM_013275.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:110451050 C>T maps to NM_033121.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:33095252 G>A maps to NM_032139.2 F857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:33134528 C>T maps to NM_032139.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:145562645 A>G maps to NM_144698.3 Q778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:98169645 C>A maps to NM_025190.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:132150906 C>T maps to NM_175873.4 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:197954685 A>G maps to NM_001195144.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr23:118893525 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:99145153 G>A maps to NM_152788.3 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr16:21261507 C>A maps to NM_145865.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:6031878 G>A maps to ENST00000356134 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:150193063 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:90349268 G>A maps to NM_001150.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:46122111 C>A maps to NM_001128324.1 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr4:169049236 G>A maps to NM_007193.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:124701111 G>A maps to NM_001003954.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:150959103 C>A maps to NM_003568.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr22:29754888 C>T maps to NM_001127.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr16:71823358 C>A maps to ENST00000423132 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:24033539 A>G did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:15864063 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:114438409 C>T maps to NM_006594.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr12:99106174 C>T maps to NM_181861.1 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:112151215 G>T maps to NM_001127510.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:1460849 C>G maps to NM_005883.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:1453535 C>T maps to NM_005883.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr14:20925651 A>T maps to NM_080649.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:21256328 G>A maps to NM_000384.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr2:21229149 C>A maps to NM_000384.2 V3530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:7803650 A>G maps to NM_001644.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:39441499 C>T maps to NM_145298.5 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:195300765 G>T maps to ENST00000421243 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:84301494 C>A did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr21:27277387 A>T maps to NM_000484.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47424687 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:68111282 T>C maps to NM_006421.3 Q1812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr20:47605194 G>A maps to NM_006420.2 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:47630160 C>T maps to NM_006420.2 R1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:32929514 T>G maps to NM_014783.3 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:43474151 C>T maps to ENST00000428638 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr3:119013765 T>A maps to NM_020754.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:36273379 G>A maps to ENST00000007510 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr23:130220395 A>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:153179297 G>A did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:153175624 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:11682851 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:11162028 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:11187705 C>A did not map to a codon.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr12:57871400 G>T maps to ENST00000393797 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr8:1871978 G>A maps to ENST00000398564 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:7516087 C>T maps to NM_001130955.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135757211 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135764990 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135827454 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:62893984 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:27057893 C>G maps to NM_006015.4 Y534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:27106464 C>T maps to NM_006015.4 Q2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:27100373 T>G maps to NM_006015.4 Y1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:46246345 A>G maps to NM_152641.2 G1480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr5:53467718 G>A maps to NM_019087.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:66525566 G>T maps to NM_018120.4 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr10:23292318 C>T maps to NM_173081.3 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:31471144 T>G maps to ENST00000408912 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:100911795 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101858221 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr11:13393791 C>T maps to ENST00000403290 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:35778808 G>A maps to ENST00000458225 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr23:69489950 C>T did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:74985230 C>A maps to NM_004041.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr5:78280983 G>A maps to NM_000046.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:78076219 C>A maps to NM_000046.3 *534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:2828697 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:2835913 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:2861176 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:2947302 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:94891002 G>C maps to NM_198150.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:19959450 G>A maps to NM_001670.2 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:25031206 G>T did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr2:9519168 G>C maps to NM_003887.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:23767954 G>T maps to NM_017707.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:15272960 C>A did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:15272961 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:103352600 C>A maps to NM_004316.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:119226903 G>T maps to NM_014034.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr8:37993283 G>A maps to NM_004674.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr16:29917115 C>T maps to NM_181718.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:29912570 G>A maps to NM_181718.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:197111683 C>T maps to NM_018136.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr17:79974987 G>A maps to ENST00000306729 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:176903402 G>A maps to ENST00000281881 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr9:119582945 C>T maps to ENST00000313400 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:117024854 A>G maps to NM_130768.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:1391259 C>T maps to NM_001039211.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:96798989 C>A maps to NM_018036.5 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr23:107374495 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:51057741 A>C maps to ENST00000358385 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:108165728 C>T maps to NM_000051.3 R1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr15:25928531 C>T maps to NM_024490.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:182584219 A>G maps to NM_014616.1 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:182591615 C>T maps to NM_014616.1 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:138882231 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:138901567 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:138880863 G>A did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr3:194181554 A>G maps to NM_024524.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:193188756 G>A maps to NM_032279.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:193207520 C>A maps to NM_032279.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:160141102 G>A maps to NM_144699.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:160124941 C>T maps to NM_144699.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:152845519 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:203691693 C>T maps to NM_001001396.1 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:153663761 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153663730 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:87165042 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:87155103 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:77298881 A>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:1802612 C>A maps to NM_138813.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:50152665 G>T maps to NM_024837.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr3:142168366 C>T maps to NM_001184.3 P2613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:142281163 C>T maps to NM_001184.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:76889124 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:76907619 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:76888736 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:76813006 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:13337044 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:13337600 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:54948492 A>G maps to NM_198437.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr17:79180596 C>T maps to ENST00000269392 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:160804161 T>C maps to NM_033168.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:118948739 C>T maps to NM_212543.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:177031296 C>T maps to NM_007255.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:1394063 C>T maps to NM_003933.4 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr6:33541651 G>A maps to ENST00000360661 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr9:134351700 C>T maps to NM_013318.3 S1395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:171511147 G>T maps to ENST00000392078 E1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:66298468 G>A maps to NM_024649.4 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:94032977 G>A maps to NM_003567.2 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr20:52612493 G>A maps to NM_003657.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:127519169 G>T maps to NM_016567.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:80912854 G>T maps to NM_183050.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:60689470 A>G maps to NM_022893.3 T192T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ND-A4WC-01A-21D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr6:136597334 G>C maps to NM_014739.2 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:81279167 C>T maps to NM_017429.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr23:39933117 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129150156 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129147294 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129148944 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:96730612 G>A maps to NM_000710.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:18230696 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:56882099 C>T maps to NM_152731.2 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:102564537 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:102005203 G>T did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:61637711 G>A maps to NM_080606.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:78417159 C>T maps to NM_001713.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr15:40398007 G>A maps to NM_001003940.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:50659511 T>C did not map to a codon.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr23:50659328 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr6:7845379 C>T maps to NM_001718.4 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr10:43317507 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:15549499 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:13603705 G>A maps to NM_148894.2 F1606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:13605282 C>A maps to NM_148894.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:65916137 C>T maps to ENST00000321892 S1938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:154305492 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154319105 G>T did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:50216635 G>A maps to ENST00000342989 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:50216636 G>T maps to ENST00000342989 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:59886055 C>T maps to NM_032043.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135570693 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:79973118 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79979251 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79947406 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79980448 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79932178 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79932798 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:79951424 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:108010897 C>T maps to NM_001018072.1 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:26508796 C>T maps to NM_001732.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:180374587 C>T maps to NM_001040462.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:40502377 G>A maps to ENST00000412359 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:99013773 G>A maps to NM_003910.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:121600380 G>A maps to NM_024834.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:99968023 A>G maps to ENST00000314594 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:120450801 C>A maps to NM_153810.4 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:50901854 G>T maps to NM_182554.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:105923952 G>A maps to ENST00000389588 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:115527102 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr11:111753231 T>C maps to NM_022761.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:64876789 C>T maps to NM_013265.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:33581396 C>T maps to ENST00000389726 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr11:122805247 C>T maps to NM_024806.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr12:49054402 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:112673047 T>C maps to NM_001109662.2 P1744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:93100660 C>A maps to NM_001037671.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:46942915 C>T maps to NM_025113.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:103419690 C>A maps to NM_138779.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr13:37269481 T>C maps to NM_203451.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr14:45711964 G>T maps to NM_018353.4 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:74823941 G>A maps to NM_018228.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:77844234 T>C maps to NM_001010860.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr14:95921743 G>A maps to NM_152592.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:95884213 G>A maps to NM_152592.3 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:24921415 G>A maps to NM_018958.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:24922006 G>A maps to NM_018958.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr15:24922693 C>T maps to NM_018958.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:76462185 C>A maps to NM_152335.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:90167616 C>G maps to NM_152259.3 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr16:3543945 G>A maps to NM_001080524.1 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr17:8092944 G>A maps to NM_017622.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:34182688 G>A maps to NM_152781.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:57288857 T>C maps to NM_018149.6 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:52265363 C>T maps to NM_173629.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:51898952 G>T maps to ENST00000382911 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:30193873 G>A maps to NM_001031726.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:58472792 C>T maps to NM_152474.4 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:1234624 G>C maps to ENST00000382477 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr19:36259087 C>G maps to NM_001039887.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:119760239 T>C did not map to a codon.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr1:22986092 C>T maps to NM_000491.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr13:24895246 C>T maps to NM_178540.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr12:7249403 G>A maps to NM_016546.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:111492550 G>A maps to NM_018372.3 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:111493954 T>C maps to NM_018372.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:57206383 C>T maps to NM_001004303.4 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr1:55277786 C>A maps to NM_001110533.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:156702120 G>A maps to NM_015997.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:55100880 C>T maps to NM_001012971.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:62187142 G>T maps to NM_024059.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:20177338 G>A maps to ENST00000389655 K575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:32784074 G>T maps to NM_014306.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:37397961 C>T maps to NM_001163857.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:73850727 G>C maps to ENST00000334126 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr2:27801238 C>T maps to NM_032266.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:24261806 G>A maps to NM_025203.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:88828940 C>A maps to NM_152670.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:29294727 G>T maps to NM_001029883.1 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:6678425 G>A maps to NM_000064.2 D1557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:43122425 G>A maps to NM_032806.4 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:56680717 C>A maps to ENST00000447900 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:57843127 C>T maps to NM_032313.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:113540666 C>T maps to NM_018392.4 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:121957766 G>A maps to NM_024574.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:184598656 G>T maps to NM_021942.4 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr5:147281274 G>A maps to NM_206966.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr5:41904474 G>C maps to NM_175921.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:47846814 G>A maps to NM_001013732.3 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:47846422 G>T maps to NM_001013732.3 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:42996872 G>C maps to NM_033112.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:151789605 T>G maps to NM_024573.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr6:170181479 C>T maps to NM_018341.1 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:40964970 T>A maps to NM_000587.2 C626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:42949407 C>T maps to NM_001099858.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr7:134853625 G>A maps to NM_024033.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr7:134851482 C>A maps to NM_024033.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr7:100815485 G>A maps to NM_198571.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:112129967 C>T maps to NM_182597.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:120876772 T>C maps to NM_024913.4 C687C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:57425734 A>G maps to NM_000066.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:57415368 T>C maps to NM_000066.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:144649982 G>A maps to NM_001100878.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:124250154 G>T maps to NM_032847.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr8:124243796 C>T maps to NM_032847.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:116187672 G>A maps to ENST00000451722 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr9:135762850 C>T maps to ENST00000372136 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:49731016 A>C maps to NM_001082534.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr8:86193463 C>G maps to NM_198584.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:15800775 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr22:24561545 C>T maps to NM_012295.3 F1653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:13482540 G>A maps to NM_023035.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:140851265 G>A maps to ENST00000277549 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:2676774 G>A maps to NM_199460.2 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:53764548 G>T maps to NM_001128840.1 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:53783417 C>A maps to NM_001128840.1 I1146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:181727968 G>T maps to ENST00000357570 E1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:49061727 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:49084858 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr16:1270129 C>T maps to NM_021098.2 S2066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:1255241 C>T maps to NM_021098.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:1267976 C>T maps to NM_021098.2 F1794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:201046077 G>A maps to NM_000069.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr3:55038788 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:1909190 G>A maps to NM_172364.4 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:62423847 G>A maps to ENST00000383709 F1241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:93065413 C>T maps to NM_001164737.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr10:75597240 C>T maps to ENST00000423381 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:3773124 G>A maps to ENST00000381771 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:110496277 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:230907845 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:230928176 C>T maps to NM_006615.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:230891100 G>T maps to NM_006615.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:34093498 G>T maps to NM_005898.4 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:19712042 C>T maps to ENST00000375145 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:2966400 G>A maps to NM_032415.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:2962373 G>A maps to NM_032415.4 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:25299942 C>T maps to NM_018272.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:25297310 A>T maps to NM_018272.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:202137359 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:122002979 C>T maps to NM_001178065.1 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr1:10715750 G>A maps to NM_001079843.1 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:26527325 C>T maps to NM_198137.1 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:92174487 G>A maps to NM_024764.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:74127970 G>A maps to NM_006077.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr12:54645938 A>T maps to NM_012117.2 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:97772450 C>T maps to NM_001159747.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:70546341 C>T maps to NM_018237.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:57363939 C>A maps to NM_133459.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr9:35660817 T>C maps to NM_174923.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:219883882 G>A maps to NM_194302.2 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:219895831 A>G maps to NM_194302.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:186380483 G>A maps to NM_152775.3 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:185593504 G>A maps to NM_152683.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:33370196 C>T maps to NM_032816.3 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:42799614 A>C did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr2:179702419 G>A maps to NM_173648.3 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:16612832 G>T maps to NM_014695.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:11545831 T>C maps to NM_145045.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr4:77290770 A>G maps to NM_001042784.1 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:11462748 G>A maps to ENST00000427879 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr23:49098536 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:3680363 A>G maps to NM_152492.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:43031965 G>T did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr15:74623363 C>T maps to ENST00000321288 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr3:126132949 G>A maps to ENST00000505024 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:126137313 G>A maps to ENST00000505024 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:180334345 T>C maps to NM_181426.1 E848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:94703806 G>A maps to NM_001042399.1 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:62530762 C>T maps to NM_138363.1 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:62518817 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:128757723 T>G maps to NM_024768.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:93104220 C>G maps to NM_181645.3 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:112335657 G>A maps to ENST00000447230 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr11:64112226 G>A maps to NM_032251.5 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:26483532 G>A maps to NM_000730.2 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr17:34310905 G>A maps to NM_032962.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:50085295 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:50053472 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:77969710 G>A maps to NM_006835.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:208591567 C>T maps to ENST00000295414 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:46415316 C>A maps to NM_001100168.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr17:38711152 G>A maps to NM_001838.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:117552697 A>G maps to NM_004258.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:7639347 A>C maps to NM_004244.4 Y735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:66479941 C>T maps to NM_005582.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:28948596 G>T maps to NM_001178098.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:158225932 G>A maps to NM_001763.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:158263086 G>A maps to NM_001765.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr11:66082812 A>G maps to NM_020404.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:72473653 C>T maps to NM_007261.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:72470734 T>C maps to NM_007261.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:72539094 G>A maps to NM_006678.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr17:72541015 G>A maps to NM_006678.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:80290414 C>T maps to NM_001127444.1 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135741500 T>G did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:207499028 T>C maps to NM_001114752.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:149983347 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:45216209 A>C maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr14:103400063 C>T maps to NM_006035.3 P1707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:65088725 C>T maps to NM_006779.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:24535872 G>A maps to NM_006727.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:24509886 G>A maps to NM_006727.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:83816997 C>A maps to ENST00000268613 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr20:44856147 G>T maps to NM_021248.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:44803549 G>A maps to NM_021248.1 F694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr20:58569314 G>T maps to NM_177980.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:58567517 G>T maps to NM_177980.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr20:58533810 G>C maps to NM_177980.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr20:59829993 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr5:26881649 G>A maps to NM_016279.3 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:176004717 G>A maps to NM_001171976.1 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:617617 A>G maps to NM_021924.4 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:47085769 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr9:90584734 G>A maps to NM_001039803.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr23:18622157 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:18622737 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:18638064 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:18626973 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr23:139865784 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:139865860 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr13:28537413 C>T maps to NM_001265.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:4892428 C>T maps to ENST00000328908 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr19:42223864 C>G maps to NM_004363.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr15:72608245 G>A maps to NM_052840.4 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:68372633 C>T maps to NM_001812.2 K641K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100387278 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:25458143 C>A maps to NM_018451.3 E1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:25480674 C>A maps to NM_018451.3 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr4:56847394 T>C maps to NM_025009.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:56878112 C>T maps to NM_025009.3 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:49083510 C>A maps to NM_001194998.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:34091279 C>T maps to NM_007186.3 R1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:95262875 C>T maps to NM_018131.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr3:138290179 C>A maps to NM_024491.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr5:639301 C>T maps to NM_018140.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:182412415 G>A maps to NM_001030311.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:580626 C>A maps to NM_004066.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:151997816 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr1:196714953 A>G maps to NM_000186.3 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:117230479 G>T maps to NM_000492.3 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:27324189 T>C maps to ENST00000404694 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr17:48545805 G>A maps to NM_001267.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:6703715 C>T maps to ENST00000309577 W741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr12:6710696 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:6709137 G>T maps to ENST00000309577 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:29091231 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:424188 G>T maps to NM_006614.2 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:391105 G>T maps to NM_006614.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:85211372 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:85218874 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:89944397 C>A maps to NM_012124.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:74421961 C>A maps to NM_015424.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr20:61981955 G>A maps to NM_000744.5 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:42611405 G>T maps to NM_004198.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:233393336 C>T maps to NM_000751.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:101011978 A>G maps to NM_004854.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr3:142840558 C>T maps to NM_004267.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:46433854 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:34263625 C>T maps to NM_022467.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr19:34263304 T>C maps to NM_022467.3 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:24496351 G>A maps to NM_031422.4 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr15:43891377 C>T maps to ENST00000413657 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:122120866 G>A maps to NM_015282.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:87036849 G>T maps to ENST00000263723 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:10153097 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:10174813 G>T did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:49845342 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:11888618 T>C maps to ENST00000376496 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:10124261 G>T maps to ENST00000355690 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:14705454 G>T maps to ENST00000417570 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:157218886 C>A maps to NM_001195555.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr12:92821901 G>A maps to NM_001025232.1 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:36214034 G>A maps to NM_022111.3 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:140281659 C>A maps to NM_022131.2 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:79028698 G>T maps to NM_153610.3 E1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:99006195 C>T maps to NM_001298.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:57950064 G>A maps to NM_001297.4 R729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:87680282 G>A maps to NM_019098.4 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:87588270 C>A maps to NM_019098.4 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:21581354 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:21670531 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:101124758 C>T maps to NM_020348.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:32778913 T>C maps to NM_015442.1 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr7:135080617 C>T maps to NM_001190850.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:3097837 G>A maps to NM_175607.1 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:99872787 G>A maps to NM_014361.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:40839787 C>T maps to NM_003632.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:40847635 G>A maps to NM_003632.2 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:147914500 G>A maps to NM_014141.5 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:146818171 C>A maps to NM_014141.5 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:147869472 A>C maps to NM_014141.5 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:76587180 A>G maps to NM_033401.3 E1147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr16:76555942 A>T maps to NM_033401.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:76528915 C>T maps to NM_033401.3 C729C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:165551578 C>A maps to ENST00000392717 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:70548412 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr13:40297489 A>C maps to ENST00000255468 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:103453187 C>A did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr8:121238998 T>A maps to NM_021110.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr6:70646732 C>A maps to NM_001858.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr20:61951482 C>T maps to ENST00000326996 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:107834448 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107869522 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107936061 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107863489 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:107420158 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:107408630 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107420146 A>G did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr9:137620520 G>T maps to NM_000093.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr9:137653811 C>T maps to NM_000093.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:10078752 A>G maps to NM_015719.3 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr21:47552222 C>T maps to NM_001849.3 H939H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:238268775 G>A maps to NM_004369.3 N2079N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:71004213 G>A maps to NM_001851.4 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:139078197 A>G maps to NM_004766.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:27945806 C>G did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr10:101491746 G>A maps to NM_078470.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr4:73930518 G>A maps to NM_173827.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:120878306 G>A maps to NM_004373.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr12:120876299 C>T maps to NM_004373.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:19547869 A>G maps to NM_014711.4 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:57180016 C>T maps to NM_152727.5 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:57155660 C>T maps to NM_152727.5 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr3:131404726 G>A maps to ENST00000502818 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:39161528 C>T maps to NM_153634.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:211469845 A>G maps to NM_001122633.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:29111426 C>A maps to NM_031311.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:88009146 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:8621304 G>A maps to NM_001014447.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:207679360 C>T maps to NM_000651.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr1:207790016 C>T maps to NM_000651.4 C2253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr1:197411422 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr7:28547288 C>T maps to NM_182898.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:3817822 C>A maps to NM_004380.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr17:43907498 C>A maps to NM_001145146.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:46851311 G>A maps to NM_014171.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:49803103 A>G maps to NM_001131.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:111779673 G>T maps to NM_001885.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:97655649 C>A maps to ENST00000182096 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:149435832 G>A maps to NM_005211.3 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1407679 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1428453 T>A did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr23:1414327 G>C did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:3216671 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:2796121 G>T maps to NM_033225.5 V3560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr1:34192254 G>A maps to ENST00000373381 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:34006218 A>C maps to ENST00000373381 T3139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:113358407 A>C maps to NM_198123.1 G2120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr8:113254009 A>G maps to NM_198123.1 G3469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:113529437 C>T maps to NM_198123.1 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:122927092 A>G maps to NM_001044723.1 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:47618876 G>A maps to ENST00000383738 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:100079127 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100088307 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:134948066 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr4:1232003 G>A maps to NM_001328.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:126682452 G>A maps to NM_022802.2 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:67645131 G>T maps to NM_006565.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:44789311 G>A maps to NM_016396.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr10:67862962 G>A maps to NM_013266.2 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:57573507 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:11018148 C>T maps to NM_001332.2 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr10:16882376 G>C maps to NM_001081.3 T3328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:16948355 G>A maps to NM_001081.3 G2586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:119670795 G>T did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr7:101747647 C>T maps to ENST00000360264 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr10:44873205 C>A maps to NM_001178134.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:47811721 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:47809355 G>A maps to NM_001101654.1 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:30578298 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr23:35993822 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:35984784 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:35988962 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:35974223 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19947912 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:40498295 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr23:105876450 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105876449 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:23953370 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:36091419 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:139038458 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:84649907 T>G maps to NM_016230.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:156757771 C>T maps to ENST00000442283 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:83128835 T>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:83129488 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:83127902 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:143957710 C>T maps to ENST00000377675 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr8:143996606 C>A maps to NM_000498.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:38301892 G>A maps to NM_000104.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr10:135346209 T>C maps to NM_000773.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr19:41622200 C>A maps to NM_000774.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:15795926 G>A maps to NM_023944.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:47495699 T>C maps to NM_178033.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:91755657 C>A maps to NM_000786.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr8:65527730 C>T maps to NM_004820.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:77528816 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:5018860 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr14:59793304 A>T maps to NM_014992.1 K418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr5:39377322 A>G maps to NM_001343.2 N522N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:85404079 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:85969605 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:85631855 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr11:61511822 G>C maps to NM_006133.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:44098475 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:137881389 C>A maps to NM_016216.3 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:34088496 C>A maps to NM_015397.3 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:17805493 G>A maps to NM_017741.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:88885770 C>T maps to NM_152418.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:6643540 G>T maps to NM_003737.2 G3122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:36686232 G>A maps to NM_004734.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:36779843 C>A maps to NM_033403.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr16:23654274 G>C did not map to a codon.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr17:79994777 G>A maps to NM_016286.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:53619306 C>T maps to NM_001160148.1 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:38095662 G>A maps to NM_001164232.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:38097796 A>G maps to NM_001164232.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:57910666 G>A maps to NM_001195056.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:30859253 C>T maps to NM_013994.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134714990 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134713729 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:134162644 G>T maps to ENST00000452510 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:124104540 G>T maps to NM_020936.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr1:115143530 G>A maps to ENST00000393274 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr8:142175304 C>T maps to NM_014957.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:66048661 C>A maps to ENST00000443035 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:65959784 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:31579259 G>A maps to NM_144973.3 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr22:32232997 T>C maps to NM_001136029.1 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:32289730 C>T maps to NM_001136029.1 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr8:124037228 G>T maps to NM_024295.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr7:14741317 G>A maps to NM_004080.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:186024713 G>A maps to NM_001346.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr13:42763365 C>G maps to NM_178009.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:137339500 C>A maps to NM_004717.2 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:50167261 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:50129445 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr11:46397945 C>T maps to NM_001105540.1 D908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:55349323 C>G maps to NM_014762.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr11:71155947 G>A maps to NM_001360.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:52365372 C>A maps to NM_001031719.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr17:21075509 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:30639045 T>C maps to NM_003587.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr3:47889848 A>G maps to NM_138615.2 Q822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:47856556 C>A maps to NM_014681.5 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr20:37634872 C>A maps to NM_021931.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:37601233 T>C maps to NM_021931.3 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:39055482 G>A maps to NM_198963.1 R880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:182850452 C>T maps to NM_001357.4 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140951544 C>T maps to ENST00000398557 E807E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:96192337 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:95940098 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr9:93375838 G>A maps to NM_017594.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr13:73346314 G>A maps to NM_014953.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:231935885 G>A maps to NM_001164537.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154004473 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:54076092 G>T maps to NM_012242.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:69699083 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:79552203 C>T maps to NM_004747.3 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:1581003 G>A maps to ENST00000357934 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:55629730 G>T maps to NM_014750.4 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:55625459 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr10:124389945 C>T maps to ENST00000368915 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:32305741 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:32404482 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:32827712 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:31947828 T>G did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:31525449 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:78350096 T>C maps to NM_013391.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:46274874 G>A maps to NM_004409.3 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:42351809 C>T maps to ENST00000427618 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:42352861 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:52431060 G>A did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr3:52395769 G>A maps to ENST00000273600 A1656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:124371783 G>A maps to NM_207437.3 A2855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:124326057 G>T maps to NM_207437.3 E1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr7:21805152 G>A maps to NM_003777.3 Q3023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:21675656 C>T maps to NM_003777.3 R1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:21747357 G>A maps to NM_003777.3 Q2203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr7:21757422 G>A maps to NM_003777.3 R2345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr17:76490707 G>A maps to ENST00000389840 D2065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:7702524 C>T maps to NM_020877.2 I2888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:7660534 C>T maps to NM_020877.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7707669 G>T maps to NM_020877.2 V3023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7678156 C>T maps to NM_020877.2 R1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:20974800 C>A maps to NM_017539.1 G3469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:20944631 A>C maps to NM_017539.1 Y4065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:21157310 G>T maps to NM_017539.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:21145623 C>T maps to NM_017539.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr5:13865874 G>T maps to NM_001369.2 Y1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:13753428 C>T maps to NM_001369.2 T3595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:13766093 C>T maps to NM_001369.2 Q3364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:196834763 C>A maps to NM_018897.2 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:196722255 A>G maps to NM_018897.2 H2753H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:196825182 C>A maps to NM_018897.2 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr6:38942306 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:38810147 G>T maps to ENST00000327475 E1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:11573030 C>A maps to NM_001372.3 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr16:46993253 G>A maps to NM_005880.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr10:74096298 C>T maps to NM_017626.4 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:128181452 G>A maps to NM_153330.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr3:132202304 C>G maps to NM_015268.3 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr16:3707024 C>T maps to NM_005223.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:230411674 C>T maps to NM_139072.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:32884446 T>C did not map to a codon.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr10:101715316 C>G maps to ENST00000342239 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr20:31381339 A>G did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr16:30021384 G>A maps to NM_003586.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr10:128785805 G>A maps to ENST00000398025 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:128795080 G>A maps to ENST00000398025 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:117817046 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:51413216 C>T maps to NM_004947.4 V1817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:111423965 G>A maps to ENST00000428084 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:111541792 G>A maps to ENST00000428084 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr19:11327691 G>A maps to ENST00000319867 T1264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr9:368134 G>A maps to NM_203447.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:3475358 C>T maps to ENST00000389653 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:83806835 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:37626107 C>T maps to NM_005128.2 V1720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:73138002 G>A maps to NM_012074.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:16302287 C>A maps to NM_206831.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr2:116593797 C>T maps to NM_020868.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:116598355 T>G maps to NM_020868.3 L738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:66259174 C>T maps to NM_005700.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:154667693 C>T maps to NM_130797.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:95800137 C>A maps to NM_181787.2 S622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:26481665 C>T maps to NM_001197293.1 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:9784645 C>T maps to NM_000798.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100500052 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:28712593 T>C maps to NM_024421.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:28651724 G>A maps to ENST00000438199 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:28671062 C>T maps to ENST00000438199 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr21:41648104 C>A maps to NM_001389.3 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:120850596 C>T maps to NM_024094.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:65180564 T>C maps to NM_032160.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:7585360 C>T maps to NM_004415.2 I2622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:7585588 C>T maps to NM_004415.2 F2698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:7571653 A>T maps to NM_004415.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:56484297 G>A maps to ENST00000281662 R2076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:205126442 G>A maps to NM_015375.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr18:32428343 G>C maps to NM_001390.4 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:32459635 T>C maps to NM_001390.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:58002451 A>C maps to NM_178502.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:221879707 C>T maps to NM_007207.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:74000941 C>A maps to NM_003584.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr17:7129435 C>G maps to NM_004422.2 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:102506037 C>T maps to NM_001376.4 L3887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr11:103182701 T>C maps to NM_001080463.1 A3870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:44021613 C>T maps to NM_001193464.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:40316672 C>T maps to NM_004714.1 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:206821769 C>T maps to NM_003582.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr2:207569604 G>A maps to NM_001093730.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:55759160 T>G maps to NM_130810.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:19251846 G>A maps to NM_024680.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:2282536 C>T maps to NM_004424.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr8:25715960 G>A maps to NM_022659.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr3:183995213 C>T maps to NM_014693.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:83239261 C>A maps to NM_005711.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:44035548 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:106763210 C>A did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr4:110866381 A>C maps to NM_001963.4 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr5:38451443 C>T maps to ENST00000354891 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:63053310 C>A maps to NM_015252.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr6:31848028 G>A maps to ENST00000395728 G1212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:39846028 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:37374084 C>A maps to NM_001135651.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:67847475 C>T maps to NM_004094.4 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:32677667 G>A maps to NM_003908.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:120816462 C>T maps to NM_003750.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr22:36919949 C>T maps to NM_003753.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr1:32694779 C>A maps to NM_003757.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:99823085 C>T maps to NM_001130679.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:37264563 C>T maps to NM_014800.9 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:60053345 G>T maps to NM_024930.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:100376648 C>A maps to NM_001008707.1 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:62374544 A>C maps to ENST00000278845 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:89131692 G>A maps to ENST00000380664 R1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129768978 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129843232 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:27760901 G>A maps to ENST00000449599 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:132479476 G>T maps to ENST00000333577 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:131201346 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:32561053 A>G maps to NM_025209.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:16456083 G>A maps to NM_004431.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:22928122 C>T maps to NM_020526.3 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:22919927 C>A maps to NM_020526.3 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:134880996 G>A maps to NM_004441.4 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr7:142562259 C>A maps to NM_004445.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:144945054 G>A maps to NM_031308.1 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr8:144940731 C>T maps to NM_031308.1 L2230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr5:65370849 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:71425341 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:71425103 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:39775497 G>A maps to NM_001136154.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:5787227 A>G maps to NM_024896.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr20:13763374 T>A maps to NM_016649.3 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr14:76928924 C>T maps to NM_004452.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:216680420 G>A maps to NM_001438.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr23:103498921 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:103495019 C>T did not map to a codon.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr23:103499130 G>A did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:103497473 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:159627344 C>T maps to NM_004453.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr16:67219059 G>A maps to NM_178516.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:72740313 C>A maps to NM_015189.1 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr9:37784999 G>A maps to NM_016042.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:122724126 G>A maps to NM_001034194.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:122728756 T>C maps to NM_001034194.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:108385312 T>C maps to NM_015065.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr8:28574907 C>T maps to NM_001440.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:148543632 C>A maps to NM_004456.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr13:113803455 C>T maps to NM_000504.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:113777239 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:197008507 C>A maps to NM_001994.2 *662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr5:76115088 G>T maps to NM_005242.4 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:169529840 G>A maps to ENST00000367796 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:169511761 C>A maps to ENST00000367796 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:154185346 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:154197758 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:154157052 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154157018 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154158061 T>C did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:138642949 T>G did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:138630628 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:57337041 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:57407417 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:82373691 C>A maps to NM_001080526.1 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:14709677 G>A maps to NM_031453.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:133922765 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:133988253 A>G did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:63410191 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr23:63410057 G>A did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:63411430 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:131521460 C>T maps to NM_001105195.1 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:71233776 C>A maps to NM_001162529.1 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr8:139164616 G>A maps to NM_015912.3 R701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:139164632 G>A maps to NM_015912.3 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:139164902 G>T maps to NM_015912.3 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr5:177156484 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:18950822 C>A maps to NM_153707.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:6238901 C>T maps to NM_032127.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:116593062 G>T maps to NM_020940.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:62067001 A>G maps to ENST00000404929 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr14:74407729 G>A maps to NM_152445.1 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:122121664 C>T maps to NM_014367.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:79598746 G>T maps to NM_016010.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:99871608 G>A maps to NM_198507.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:36788048 C>A maps to NM_018166.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr10:102689754 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:119301347 G>A maps to NM_024581.4 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr12:49999202 G>A maps to NM_032130.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:18694242 C>T maps to NM_016078.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:176951477 G>A maps to ENST00000442143 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:103411475 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr10:124608783 G>A maps to NM_152644.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:10671630 G>A maps to NM_022068.2 R2718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:120877029 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:34148673 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:34962327 G>A did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:37028480 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr2:16742750 G>T maps to NM_030797.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:177199125 G>A maps to NM_021165.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:190067522 C>T maps to NM_199051.1 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:190067974 G>A maps to NM_199051.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:67579899 C>T maps to NM_001193523.1 R1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:119425180 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:212798593 G>A maps to NM_153606.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:50979570 G>T maps to ENST00000391816 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr8:12285187 G>A maps to NM_001137610.1 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:85135933 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:35424066 C>T maps to NM_021922.2 D264D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ND-A4WC-01A-21D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr14:45623209 A>C maps to NM_020937.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:127668791 G>T maps to ENST00000368692 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr2:242380726 A>C maps to NM_014808.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:13039264 G>T maps to NM_004461.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:223513463 C>A maps to NM_005687.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:172633519 C>T maps to NM_000639.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:80040212 G>T maps to NM_004104.4 T1999T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:80049218 G>A maps to NM_004104.4 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:187509883 G>A maps to ENST00000260147 T4546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:187509931 G>A maps to ENST00000260147 F4530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:187542356 G>A maps to ENST00000260147 R1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:92624209 C>T maps to ENST00000298047 S4567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:126371570 G>T maps to NM_024582.4 E3134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:126370223 C>T maps to NM_024582.4 R2685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:126240856 A>G maps to NM_024582.4 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:126240329 G>T maps to NM_024582.4 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:92353566 C>A maps to ENST00000267620 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:48776135 G>A maps to NM_000138.4 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:107197555 G>A maps to NM_001163315.2 N657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:77581884 C>A maps to NM_012158.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:15642452 A>C maps to NM_012161.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:28314408 C>T maps to NM_172366.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:139836498 G>A maps to NM_018998.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:159277720 G>T maps to ENST00000368115 *261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:40411751 G>A maps to NM_003890.2 A1292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:120927160 C>T maps to NM_001017986.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr5:72364496 T>G maps to NM_138782.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:72552577 G>A maps to ENST00000409314 Y683Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr9:137808191 A>G did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:157665944 C>A maps to NM_052939.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:157551319 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:161697299 G>T maps to NM_001002901.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:108203562 C>T maps to NM_005246.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:108203562 C>T maps to NM_005246.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr8:125082753 G>A maps to NM_001039112.2 W1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr8:125076586 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr19:35941554 C>T maps to NM_005306.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:155505566 G>A maps to NM_000508.3 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:155507461 C>T maps to NM_000508.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:32754279 C>A maps to NM_139241.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:32751468 A>G maps to NM_139241.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr5:44305204 C>A maps to NM_004465.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr23:137717784 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:102379129 C>A maps to NM_175929.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:176519358 C>T maps to NM_213647.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1017701 C>T maps to NM_021923.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:155533542 G>A maps to ENST00000407946 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:34298176 G>A maps to NM_025135.2 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:47260140 C>T maps to NM_024301.4 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:152278955 G>A maps to NM_002016.1 H2802H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152278697 T>G maps to NM_002016.1 G2888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152284532 T>G maps to NM_002016.1 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:152283913 G>A maps to NM_002016.1 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152325749 G>A maps to NM_001014342.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:21542506 C>T maps to NM_018071.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr9:84608176 C>A maps to NM_001001670.2 S931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:153581769 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:153581006 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:153588428 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:153595789 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:153590695 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153593317 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153581371 C>T did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr23:153592411 C>G did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr23:153578522 G>A did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr23:153588158 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr13:28931760 T>C maps to NM_002019.4 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:28602425 C>A did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr5:180048620 G>A maps to NM_182925.4 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:33261468 G>T maps to NM_001103184.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:240635743 C>T maps to ENST00000406993 D1854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:147030227 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:159642726 A>T maps to NM_032532.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:49776034 T>C maps to NM_001079673.1 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:28626993 T>C maps to NM_005253.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr20:22563664 G>T maps to NM_021784.4 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:80545020 G>T maps to NM_004514.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr14:89628876 C>A maps to NM_001085471.1 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:114282502 G>T maps to NM_148898.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr23:55650342 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:74670324 G>A maps to NM_003838.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:52271958 C>A maps to NM_001005738.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:44180392 G>A maps to NM_032892.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr9:37745608 C>T maps to NM_014907.2 Q1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:37740147 C>T maps to NM_014907.2 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:37745052 T>C maps to NM_014907.2 H1008H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr10:49395265 G>A maps to NM_001018071.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:12693028 T>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:12735884 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:12735696 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:44975940 C>A maps to NM_032135.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:5645074 C>T maps to ENST00000340250 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr7:127235408 C>T maps to NM_020369.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:127239487 C>T maps to NM_020369.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:132553061 G>T maps to NM_015082.1 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:162841648 C>A maps to NM_020116.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:31089557 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr1:24186287 C>T maps to NM_000147.4 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:5867214 G>A maps to NM_002034.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:96651945 C>T maps to NM_006581.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:111983094 G>A maps to NM_153047.1 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr7:90895679 C>G maps to NM_003505.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr17:42636255 C>G maps to NM_001466.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:72849233 C>T maps to NM_003508.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:42152411 C>A maps to NM_138387.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:153762333 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:78078717 C>T maps to NM_001079804.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:17488842 C>T maps to NM_001037814.1 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr21:27141431 C>T maps to NM_002040.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr5:161318009 C>G maps to NM_001127648.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:46252591 C>T maps to ENST00000507069 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:151358216 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:151424407 G>A did not map to a codon.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr5:161128592 G>T maps to NM_000811.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr5:161113260 G>T maps to NM_000811.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr5:160721269 G>A maps to NM_021911.2 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:160761810 G>A maps to NM_021911.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:26793008 C>T maps to NM_021912.4 W451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:151123931 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:101594116 C>T maps to NM_024642.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr12:4855405 C>T maps to NM_017417.1 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:34073282 G>A maps to NM_139285.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr22:30682352 C>T maps to NM_001037666.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:104130494 C>T maps to NM_004193.2 R1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:89585911 G>A maps to NM_004120.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:89730614 G>A maps to NM_052942.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:10556715 C>T maps to NM_001491.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:74817651 A>G maps to ENST00000238018 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr8:97172605 G>C maps to NM_001001557.2 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:69652183 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:76990352 A>G maps to ENST00000376217 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:23967197 G>A maps to NM_178311.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr7:100281656 C>T maps to NM_022574.4 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr7:150269568 C>A maps to ENST00000430830 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr7:150269307 C>T maps to ENST00000430830 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:150217464 G>T maps to NM_153236.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr6:121768820 T>C maps to NM_000165.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:90605647 G>A maps to NM_032602.1 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:35259969 C>T maps to NM_002060.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:39340702 T>C maps to NM_030772.4 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70444063 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:30709250 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100653891 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:131302552 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr2:121732501 C>A maps to NM_005270.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:42116367 C>T maps to NM_000168.5 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:42005604 C>T maps to NM_000168.5 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:54060080 C>T maps to NM_147193.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:673155 G>A maps to ENST00000397393 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48624298 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:17691985 G>A maps to NM_024656.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr3:52324394 C>T maps to NM_145262.3 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr5:150646987 C>T maps to NM_000405.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr19:19741120 G>C maps to NM_016573.2 S855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:56377720 C>T maps to NM_138736.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:19776480 C>G maps to NM_053004.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:52416725 G>A maps to NM_016194.3 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:84967542 G>C maps to NM_005274.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:37368057 G>T maps to NM_001172713.1 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr8:41363428 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:121410022 C>A maps to ENST00000393667 E2730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:121435638 G>A maps to ENST00000393667 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:167754716 A>G maps to NM_014498.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:170508561 C>T maps to NM_152281.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:101163311 G>A maps to NM_002079.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:101157416 C>A maps to NM_002079.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr16:20331091 T>C did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr10:113928672 G>A maps to NM_020918.4 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:96690525 G>A maps to NM_207328.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:96690544 C>T maps to NM_207328.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:33604671 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:156565381 G>A maps to NM_015590.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr17:42478775 T>C maps to NM_001002909.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:56545381 A>G maps to NM_001127236.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:132888170 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:132437256 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:24473847 A>G maps to NM_001503.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:136112732 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:46995497 C>T maps to ENST00000283297 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr23:135475714 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135430315 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135426789 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr3:100364804 C>T maps to NM_032787.2 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:105518407 C>T maps to NM_013345.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:20043161 A>G maps to NM_001002911.2 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:9709431 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:98251632 C>A maps to NM_005290.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:67219700 G>A maps to NM_206997.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:175306890 G>T maps to NM_152529.5 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:25464417 C>T maps to NM_020752.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41555423 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41555867 T>G did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr2:133174752 G>A maps to NM_001508.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:174417470 T>C maps to NM_005684.4 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19032030 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19009002 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:8588798 C>A maps to NM_080819.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:145765392 A>G maps to NM_001097612.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr16:57717866 C>G maps to NM_170776.4 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:90087049 C>T maps to NM_032119.3 R4802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr23:101911929 G>T did not map to a codon.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr23:101912151 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101912217 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101911591 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr23:101972266 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101970233 C>T did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr12:13061635 A>G maps to NM_003979.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr12:13103267 G>A maps to NM_018654.1 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr5:150405019 G>A maps to NM_002084.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:37899523 C>T maps to ENST00000445327 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:10104054 C>T maps to NM_198182.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr23:122387245 C>A did not map to a codon.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr23:122599592 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:122460030 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:122460037 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:122561804 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:122616805 T>C did not map to a codon.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr11:105483156 C>T maps to NM_000829.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:87614321 C>T maps to NM_017551.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:87484238 A>G maps to NM_017551.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:87362272 G>T maps to NM_017551.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:93511402 T>G maps to NM_001510.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr21:31045467 T>C maps to ENST00000327783 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:102372595 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:37325528 G>A maps to NM_000831.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:120690495 C>T maps to NM_014619.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:42509902 G>T maps to NM_002088.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48839392 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:146708097 G>T maps to NM_000838.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:51749333 C>T maps to NM_000839.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr7:86468806 G>A maps to NM_000840.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:86416019 C>T maps to NM_000840.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr7:86468551 C>T maps to NM_000840.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:7620980 G>A maps to NM_181874.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:16170394 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:145252291 C>T maps to NM_001080516.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:51487065 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:30560724 G>T maps to NM_000637.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:24323181 G>A maps to NM_000854.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:54967831 G>T maps to NM_133267.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr13:28009311 A>T maps to NM_002097.2 K306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:27503991 G>A maps to NM_001520.3 C973C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:115335707 G>A maps to NM_004132.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr5:82940356 G>A maps to NM_001884.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:52216985 G>A maps to NM_001523.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:36108226 C>T maps to NM_015302.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr16:227403 C>A maps to NM_000558.3 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:5269668 C>A maps to ENST00000440157 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:11139869 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:11139033 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:153217410 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr23:153230116 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153227717 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153220471 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:104492165 C>T maps to NM_013320.2 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:30689246 G>A maps to NM_002110.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr5:45396743 C>A maps to NM_021072.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr17:42171101 G>A maps to NM_001015053.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48682970 G>T did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:48673985 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:71787850 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr23:71684475 T>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr23:83724415 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:83730394 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr1:236746149 T>C maps to NM_018072.5 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:37291993 G>C maps to NM_019024.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:37235919 G>A maps to NM_019024.1 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:58137337 G>A maps to NM_022070.4 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:31585632 G>A maps to NM_015382.2 V1809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:93258716 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr4:84348766 G>A maps to NM_133636.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:65418861 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:65483501 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:65418734 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:63972976 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:63970230 G>A maps to ENST00000261887 Q2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr15:28474382 G>A maps to NM_004667.4 R1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr6:26091202 C>T maps to NM_000410.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:79653377 C>T maps to NM_004712.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr4:145580926 T>C maps to NM_022475.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:46815487 C>T maps to NM_152795.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:114483988 C>A maps to ENST00000426820 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr6:27834839 C>A maps to NM_005322.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr6:26033562 G>A maps to NM_003513.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:27805760 C>T maps to NM_003510.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr6:27833146 C>T maps to NM_003511.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr6:26200067 G>A maps to NM_003522.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr6:27100484 G>A maps to NM_021058.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr6:26271423 G>A maps to NM_003534.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr6:26104423 A>T maps to NM_003542.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:26189199 G>A maps to NM_003539.3 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr1:149858535 T>G maps to NM_003517.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr6:32609249 G>A maps to NM_002122.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:185970452 G>T maps to NM_031935.2 E1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:150154630 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:79918281 C>G maps to NM_004242.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:35661202 C>T maps to NM_001003681.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:162900239 G>T maps to NM_001142556.1 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr20:43043172 C>T maps to ENST00000338692 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:83280638 C>T maps to NM_031370.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr19:39330768 G>A maps to ENST00000221419 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr7:27237843 G>A maps to NM_000522.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr17:46700471 G>A maps to NM_024017.4 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:176964702 C>T maps to NM_021193.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr2:176987825 C>T maps to NM_014213.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:100189342 G>A maps to NM_000195.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:103825881 C>G maps to NM_024747.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr8:21986671 C>T maps to NM_005144.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:21982827 C>A maps to NM_005144.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:152188527 G>A maps to NM_001009931.1 G1859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:152191668 G>A maps to NM_001009931.1 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:152193030 G>T maps to NM_001009931.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:13504290 G>A maps to NM_006042.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:132091119 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:84163650 C>T maps to NM_031463.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:104336432 G>A maps to NM_003299.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:118434330 C>T maps to NM_025015.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr14:65008091 C>T maps to NM_021979.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:132424106 G>T maps to NM_002154.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:128003020 C>T maps to NM_005347.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr1:16342194 G>A maps to ENST00000375714 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr19:55789013 G>A maps to NM_012267.4 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr1:22161367 G>A maps to NM_005529.5 F3508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135593732 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:147863827 G>T maps to NM_001040173.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:147929809 G>A maps to NM_001040173.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:38835512 T>C maps to NM_153692.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr23:53611280 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr23:53674333 G>C did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:53574726 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:53575114 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:53562434 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:53574797 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr7:8258021 C>T maps to ENST00000422063 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:203653774 C>A maps to NM_138468.4 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:45658336 G>A maps to ENST00000400379 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:2641598 C>T maps to NM_006899.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:153051889 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:131939485 G>A maps to NM_203434.2 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr12:6664976 G>A maps to NM_001193457.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:158984676 C>T maps to ENST00000295809 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr10:91162763 A>G maps to NM_001548.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:21201821 G>A maps to NM_021057.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:110618312 C>T maps to NM_014055.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:69366639 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:99500655 G>A maps to NM_000875.3 Q1363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr7:23391159 C>T maps to NM_006547.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:23387298 G>A maps to NM_006547.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:45930297 C>A maps to NM_000596.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr9:38411521 C>A maps to NM_001007563.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:68696696 C>T maps to NM_002180.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:130417107 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:130412664 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:41151134 G>A maps to NM_001080444.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:133790721 A>C maps to NM_014987.1 Y966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:117875002 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:29959903 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:29938104 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:29414548 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:104478595 A>C did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr2:102805587 T>C maps to NM_003854.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:123534040 C>A maps to NM_021803.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:67724381 A>G maps to NM_144701.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:24484263 G>A maps to NM_170743.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:55195808 C>T maps to NM_139017.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1460714 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1467356 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:35860990 C>T maps to NM_002185.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr2:239103470 G>A maps to NM_030768.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:128037025 G>A maps to NM_000883.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:76728557 G>A maps to NM_001563.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr1:62237127 C>T maps to NM_176877.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:184431544 G>T maps to NM_001564.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:134563348 G>A maps to NM_005539.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:134563303 C>T maps to NM_005539.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:118864480 T>C did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr8:19682373 T>C maps to NM_018142.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:95884163 C>T maps to NM_017864.2 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:59955837 C>A maps to NM_152230.4 *417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:51928929 A>G maps to NM_152397.2 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:75896635 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:123104993 C>A maps to NM_178827.4 G551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:227661890 G>A maps to NM_005544.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:227662587 G>C maps to NM_005544.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:107976124 G>A did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr23:107976056 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:54319318 G>A maps to NM_024336.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:33080314 G>T maps to ENST00000262650 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:182339887 T>G maps to NM_000885.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:182350654 A>G maps to NM_000885.4 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr12:54799461 G>A maps to NM_002205.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:173355989 G>A maps to ENST00000264106 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr16:31434761 C>A maps to ENST00000444228 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr17:3638131 C>T maps to NM_002208.4 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:63955790 A>G maps to ENST00000371092 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:7605312 T>C maps to ENST00000256861 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:54785155 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:226827356 T>C maps to NM_002221.3 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr3:4716885 G>A maps to ENST00000356617 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:26775333 C>A maps to NM_002223.2 E1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:24438917 C>T maps to NM_006277.2 K1330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:24509171 A>C maps to NM_006277.2 L591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:6031487 G>A maps to NM_001099433.1 D800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:133958681 G>A maps to NM_001105521.2 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr11:134009764 A>G maps to NM_032801.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr6:15497072 G>T maps to NM_004973.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:733858 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:75156774 C>A maps to NM_020647.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr14:24040295 C>T maps to NM_032452.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr23:8553428 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:8553379 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr3:20082164 G>T maps to NM_003884.4 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:41706284 G>T maps to NM_152903.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:85255046 C>T maps to NM_020122.4 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:5021795 G>T maps to NM_000217.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:111216486 G>A maps to NM_002232.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:111216963 G>A maps to NM_002232.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:111216609 G>A maps to NM_002232.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:5154875 C>A maps to NM_002234.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:75444658 G>A maps to NM_139137.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:110754450 C>T maps to NM_004978.4 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:120386009 C>T maps to NM_012281.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:119914841 C>T maps to NM_012281.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:20760462 C>T maps to ENST00000382152 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr17:21319328 G>A maps to NM_021012.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:21319490 G>A maps to NM_021012.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:138656878 C>T maps to ENST00000298480 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:196397291 C>T maps to NM_198503.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:44176932 C>T maps to NM_198353.2 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:23407999 C>T maps to NM_001009999.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:6980998 G>A maps to NM_015061.3 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:53247576 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:53222262 C>G did not map to a codon.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr23:44922730 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:55968604 G>T maps to NM_002253.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:61002591 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr7:142641780 G>A maps to NM_000420.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:6417015 G>A maps to NM_003685.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:6416503 G>A maps to NM_003685.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:6843913 C>T maps to NM_014743.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr6:24596358 C>T maps to NM_014809.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:34832662 G>A maps to NM_014686.3 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:42361620 C>A maps to NM_015058.1 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:58965565 G>A maps to ENST00000354386 E1405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:6499536 C>A maps to NM_014804.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:6493187 G>A maps to NM_014804.2 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr10:75554071 C>T maps to NM_015037.2 D931D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:29487554 T>G maps to NM_014939.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr12:105543427 C>T maps to NM_015275.1 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:105527583 G>A maps to NM_015275.1 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr9:34978095 G>A maps to NM_015297.1 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:57180405 A>G maps to NM_020722.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:24831987 G>A maps to NM_019590.3 V1263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr6:138584323 G>T maps to NM_020340.4 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:128696953 C>A maps to NM_020741.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr10:70748845 C>G maps to NM_015634.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:86542400 C>T maps to NM_001142749.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:101833269 G>T maps to NM_020802.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:94007015 G>T maps to ENST00000393153 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr8:95518909 A>T maps to NM_015496.3 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1360205 G>A maps to NM_020894.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:18378025 C>T maps to NM_001145304.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:18376864 G>C maps to NM_001145304.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr9:20862654 C>T maps to NM_017794.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:233515337 A>G maps to NM_032435.2 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr6:30647012 G>A maps to NM_133471.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:11985517 C>A maps to ENST00000376576 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:113375980 T>C maps to NM_001009899.2 Q1516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:73960122 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:8871068 G>A maps to NM_020738.2 F1699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:94408153 C>T maps to NM_004523.3 C911C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:94369266 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:91478602 T>C maps to ENST00000416354 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:91488914 G>T maps to ENST00000416354 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr12:39735321 C>A maps to ENST00000395670 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:69715498 C>T maps to NM_138555.1 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:245849740 C>T maps to NM_018012.3 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:69607078 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:149679779 G>A maps to NM_004522.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:149793853 C>A maps to NM_004522.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:55284833 A>G maps to ENST00000291633 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:55363702 G>A maps to NM_006737.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr11:126306736 G>A maps to NM_032531.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr11:126305175 G>A maps to NM_032531.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:55561831 G>A maps to NM_000222.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr14:104124026 C>T maps to ENST00000445352 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:45853652 G>T maps to NM_177417.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr14:50249132 T>G maps to NM_014315.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr6:42986289 G>C maps to NM_057161.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr1:18809451 C>T maps to NM_152375.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:117054244 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:117043458 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:24024276 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:24006620 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:21674487 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:86887421 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:86888867 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:86924354 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:86869492 T>A did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:152733336 C>T maps to NM_001025231.1 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr7:149418076 C>T maps to NM_032534.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:39681142 G>A maps to NM_002276.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:38859657 G>T maps to NM_019016.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr17:39521742 G>A maps to ENST00000394004 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:39521450 G>A maps to ENST00000394004 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr21:45994015 C>A maps to NM_198687.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:31864142 C>A maps to ENST00000433652 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:39406151 C>T maps to NM_033191.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:143718290 T>C maps to NM_003937.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr23:153131271 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:153129470 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153135091 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:62676246 G>T maps to NM_019079.4 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:42163003 C>T maps to NM_032107.4 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr18:6965301 G>A maps to NM_005559.2 R2394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:21484615 C>T maps to ENST00000416669 D2193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr20:60913125 C>A maps to NM_005560.3 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:60927342 G>A maps to NM_005560.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr20:60885520 C>A maps to NM_005560.3 L3518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:49160169 C>A maps to NM_002292.3 E1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:119565272 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:31212745 T>C maps to NM_006762.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:909779 G>A maps to NM_015155.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:45537859 A>G maps to NM_015340.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:64743515 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:64743962 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:64751317 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:36999942 G>T maps to NM_004139.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:152784987 C>A maps to NM_178349.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:152759804 C>T maps to NM_178353.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr2:136575372 C>T maps to NM_002299.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr4:16900018 G>A maps to NM_001290.3 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:226125368 G>A maps to NM_003240.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:65639661 C>T maps to NM_014319.4 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:38257890 C>T maps to ENST00000379957 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:25976005 T>C maps to NM_009587.2 *356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:71978129 C>T maps to NM_003667.2 C780C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr13:40175116 G>A maps to NM_005780.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:111874816 A>C did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr1:75608913 C>A maps to NM_001001933.1 C167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:54823807 G>A maps to NM_021250.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:55144056 C>T maps to ENST00000427581 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:50571157 C>A maps to NM_001113546.1 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:41621301 G>A maps to NM_014988.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:31658194 G>A maps to NM_001031801.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:101109702 C>A maps to NM_001040616.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:90356596 C>T maps to NM_001010939.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:90497469 C>T maps to NM_001080518.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr5:36118006 C>A maps to NM_001007527.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:126154642 A>G maps to NM_005573.3 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:69171468 G>T maps to NM_198271.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:129453168 C>T maps to NM_001174147.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr9:129453153 C>T maps to NM_001174147.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr23:118109479 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118112413 G>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr8:23167293 G>A maps to NM_002318.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr6:160999635 G>A maps to NM_005577.2 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:160977178 G>A maps to NM_005577.2 Y1617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:161027560 G>A maps to NM_005577.2 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:78010755 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:78010798 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:7090984 A>T maps to NM_005768.5 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:188590443 C>T maps to NM_005578.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr9:104086317 G>A maps to NM_017753.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:99771600 C>T maps to NM_014839.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:151821336 C>T maps to NM_006726.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr14:42360909 G>T maps to NM_152447.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:57588393 C>T maps to NM_002332.2 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr12:57572303 C>T maps to NM_002332.2 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:141607715 G>A maps to NM_018557.2 R1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:170002289 G>A maps to NM_004525.2 R4319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr11:68170952 G>A maps to NM_002335.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:3517920 G>A maps to NM_002337.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:53787464 A>G maps to NM_018214.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:194081583 C>T maps to NM_001135057.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr3:194080439 A>G maps to NM_001135057.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr8:145749617 C>G maps to NM_001024678.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:122672354 C>A maps to NM_001098519.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:45911900 T>C did not map to a codon.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr19:51022477 C>T maps to NM_001080457.1 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:131670970 C>T maps to NM_001127244.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:90048688 C>T maps to NM_015350.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr8:86038970 T>G maps to NM_033402.4 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:86027430 C>A maps to NM_033402.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:37107797 C>A maps to NM_006309.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:85450932 C>T maps to NM_001079910.1 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:85449617 A>G maps to NM_001079910.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:204588976 G>A maps to NM_201630.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr1:204588891 G>A maps to NM_201630.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:68686814 T>C maps to NM_178011.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:68687298 G>T maps to NM_178011.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr3:115805174 T>C maps to NM_002338.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:32526905 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:21207444 G>A maps to ENST00000381541 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:33413753 G>T maps to ENST00000354476 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:46497451 A>C maps to NM_002343.3 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:114536596 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:31678181 T>C maps to NM_001003693.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:13211648 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:56863329 T>C maps to NM_002350.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:24120730 C>G maps to NM_007260.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:235972296 A>G maps to NM_000081.2 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:235878564 G>A maps to NM_000081.2 S3240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr3:42448440 G>A maps to NM_144634.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr3:45877082 G>A maps to NM_020347.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr4:151504555 G>A maps to NM_006439.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:13982971 G>T maps to ENST00000310348 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:1976421 G>A maps to NM_003550.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:2188794 G>A maps to NM_003550.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:11735150 C>T maps to ENST00000376669 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:47297546 C>T maps to NM_003682.3 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:35804290 G>T maps to NM_002361.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:152482976 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:151303365 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:148798277 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:148797839 T>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:151900215 G>A did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:151899864 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:151935380 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:151935895 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:151093030 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr23:151870054 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:151869774 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:149013419 G>A did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:30268691 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr23:30236897 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:30236700 C>T did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:30236751 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:30254098 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:26212338 G>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:26212811 G>A did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:140993982 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:140996561 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:140996501 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr23:141290898 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:141291544 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:141291628 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:141291464 G>C did not map to a codon.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr23:141291112 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:140984574 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:75649800 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:75650000 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr23:75004286 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:55479289 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:65342631 T>C maps to NM_001033057.1 R1270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:10796398 C>T maps to NM_005906.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:149638112 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:118042104 G>T maps to NM_006699.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:118045592 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:109202581 C>T maps to NM_002372.2 V1106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr15:75653472 G>C maps to NM_006715.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:12483293 C>T maps to NM_018050.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:71494404 C>T maps to NM_005909.3 I1741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:17836816 C>T maps to NM_018174.4 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:210557674 G>T maps to NM_002374.3 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:21202198 G>A maps to NM_145109.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:11984699 G>A maps to ENST00000415385 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:68061959 T>C maps to NM_145160.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:40719430 C>T maps to NM_002446.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr11:65380918 A>C maps to NM_002419.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:19507019 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19379462 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr6:161530807 G>T maps to NM_005922.2 E1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:161530818 T>C maps to NM_005922.2 D1423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:71216701 G>A maps to NM_033141.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:20060637 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:20043154 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:48252488 C>T maps to NM_002747.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:31424466 G>T maps to NM_012325.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr5:10403622 C>T maps to NM_005885.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr12:57882856 C>T maps to NM_004990.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:12958186 C>T maps to NM_014975.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:152174095 A>G maps to NM_021038.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr23:131573525 G>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:54684566 G>A maps to NM_024298.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:103349202 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:112824030 G>A maps to NM_001085377.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:138724666 G>C did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr13:113748840 G>T maps to NM_001112732.1 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:182925517 G>A maps to NM_015078.2 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr22:41077055 C>T maps to NM_005297.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:100403956 C>A maps to NM_032503.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:127335928 C>T maps to NM_004526.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:52138699 C>T maps to ENST00000419835 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:47705106 G>A maps to NM_003906.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr8:48873763 C>T maps to NM_182746.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:6302631 C>T maps to NM_024596.3 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:90371186 C>T maps to NM_014611.1 K4892K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:153296732 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:29533289 G>A maps to NM_016011.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:70356868 A>G did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:70350050 A>C did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:70360622 A>G did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:70344031 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70352362 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70344098 A>C did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:70338670 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:116460309 G>A maps to NM_015335.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:40586032 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:48654088 T>C maps to NM_014166.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:42880632 A>G maps to ENST00000251268 G2748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr22:42128267 G>A maps to NM_152513.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:42141898 G>T maps to NM_152513.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:15725700 G>A maps to NM_005924.4 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:29772618 C>T maps to NM_005925.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:88766448 C>T maps to ENST00000395102 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:112786407 C>T maps to NM_006343.2 D989D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:119621740 C>T maps to NM_020961.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:196736582 G>A maps to NM_005929.5 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:196733482 G>A maps to NM_005929.5 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:196730856 T>C maps to NM_005929.5 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:179107815 C>T maps to NM_033540.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr3:179095161 C>T maps to NM_033540.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr8:145735979 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr4:128878654 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:42021387 C>T maps to ENST00000219905 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:42040967 T>G maps to ENST00000219905 L1831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr7:141736711 C>T maps to ENST00000475668 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr7:141736742 C>T maps to ENST00000475668 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:39883621 C>T maps to NM_001098270.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:99294910 C>A maps to NM_012214.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:135119888 G>A maps to NM_002410.3 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:135012114 C>T maps to NM_002410.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:88423782 G>A maps to NM_152706.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:12246316 C>T maps to NM_014632.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr11:12315220 T>G maps to NM_032867.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:38329084 C>T maps to NM_033386.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:10417565 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:10491181 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107169923 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:67423798 C>T maps to NM_001077700.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:129905828 T>C maps to NM_002417.4 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:28023450 C>A maps to NM_173576.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr10:28023622 C>T maps to NM_173576.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:20414131 C>A maps to NM_004529.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:24124644 C>T maps to NM_005940.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:102815027 G>A maps to NM_002427.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr10:127464288 C>T maps to NM_147191.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr16:3107136 C>A maps to NM_022468.4 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:90857446 G>A maps to NM_007351.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:56748712 C>A maps to NM_018365.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:2303969 G>A maps to NM_020310.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:33800115 C>T maps to NM_017947.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr11:75439190 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:106184835 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:102931708 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr12:123703046 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154007591 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:202510090 T>A maps to NM_033066.2 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:202510067 T>C maps to NM_033066.2 Q593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:94224043 C>T maps to NM_005591.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:18158856 C>T maps to NM_054031.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:13879656 C>T maps to NM_001031727.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:34958727 G>C maps to NM_024864.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:19423163 G>A maps to NM_003776.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:224822308 C>A maps to NM_022915.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:224831612 A>G maps to NM_022915.3 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr15:89021194 G>A maps to NM_022839.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:138392883 G>A maps to NM_016034.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:47707955 G>A maps to NM_000251.1 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:234775122 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:234774943 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:190922364 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:174151739 G>C maps to NM_002449.4 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:21815499 G>A maps to NM_002451.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr8:121535575 A>G maps to NM_022045.3 *905W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:242036780 A>G maps to NM_182501.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:65295411 T>C maps to NM_139242.3 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:80137563 C>T maps to NM_006441.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr2:55463903 C>A maps to NM_002453.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:149764985 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:149899984 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:31251299 T>C maps to NM_017762.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:63574753 T>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:17611441 G>A maps to NM_001001924.2 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:30071433 C>T maps to NM_001033602.2 F1223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:9014640 T>C maps to NM_024690.2 K12778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:9062452 C>T maps to NM_024690.2 E8331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:100685697 C>A maps to NM_001040105.1 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:100674924 C>T maps to NM_001040105.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:1092953 G>A maps to ENST00000441003 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:30955307 G>A maps to NM_001010909.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:1265996 G>A maps to ENST00000447027 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:105451417 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105451045 C>A did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr23:105449629 T>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr23:3235471 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:3238668 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:3242219 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:3240877 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:102038554 G>T maps to NM_002465.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:102067365 C>T maps to NM_002465.2 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:47364689 G>T maps to ENST00000399249 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr13:77713330 G>A maps to NM_015057.4 D2553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:48606123 G>T maps to NM_032133.4 G869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr12:81111291 A>T maps to NM_005593.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:81102658 C>T maps to NM_002469.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:8508285 G>T maps to ENST00000360416 L120L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ND-A4WC-01A-21D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:10441077 G>A maps to ENST00000399342 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:10427884 G>A maps to NM_017534.5 I1691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:10447241 C>A maps to NM_017534.5 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:10555850 G>A maps to NM_002470.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:10363564 G>C maps to NM_017533.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:23887558 C>T maps to NM_000257.2 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr14:23885020 G>A maps to NM_000257.2 D1658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:23902788 G>A maps to NM_000257.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr17:10304251 C>T maps to NM_002472.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:123383093 G>A maps to NM_053025.3 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr17:18023598 G>A maps to ENST00000205890 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:34854397 T>C maps to NM_001163735.1 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:8609288 G>A maps to NM_012335.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:109863800 C>A maps to NM_001101421.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:26436414 C>T maps to NM_017433.4 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:52718064 G>T maps to ENST00000358212 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:52538225 T>A maps to NM_018728.3 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr8:2021506 C>T maps to NM_003970.2 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr1:24417410 G>A maps to ENST00000330966 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr1:24390562 G>A maps to ENST00000330966 D1210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:40231701 A>G maps to NM_015460.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr3:40251349 G>A maps to NM_015460.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:62839358 G>A maps to NM_004535.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:1906945 A>G maps to ENST00000399161 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr19:59074527 C>T maps to NM_198055.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:48594764 G>A maps to NM_153029.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:30248813 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:153196293 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153195616 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr4:140272381 C>T maps to NM_057175.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:140278709 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:41933047 C>T maps to NM_024561.4 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:88622301 C>A maps to NM_024635.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr12:57111095 T>C maps to NM_001113203.1 A1406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr12:57109733 G>A maps to NM_001113203.1 V1860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:72433720 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:72433252 C>T did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:72433769 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:92927915 G>T did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr7:102760562 C>T maps to ENST00000455523 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr8:18258040 T>A maps to NM_000015.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:78400499 G>T maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr12:78362440 G>A maps to NM_014903.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:78562558 G>T maps to NM_014903.4 E1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:78225315 G>A maps to NM_014903.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:15555740 C>A maps to NM_015909.2 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:35624438 T>A maps to ENST00000400445 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr13:36242542 C>T maps to ENST00000400445 T2879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr3:47050734 G>A maps to NM_015175.1 K2730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:16892260 G>T maps to NM_017940.3 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr1:145293413 A>G maps to NM_001039703.4 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:145293413 A>G maps to NM_001039703.4 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:148594543 T>C maps to NM_001170755.1 H639H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:113102990 C>A maps to ENST00000316851 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:113102482 C>A maps to ENST00000316851 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:134073714 C>T maps to NM_015261.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:17824681 G>T maps to NM_022346.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr7:158468183 A>G maps to NM_017760.5 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr22:50955911 G>A did not map to a codon.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr9:100403881 T>A maps to NM_002486.4 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:183845982 C>A maps to NM_205842.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:124831139 C>T maps to NM_006312.4 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:23931764 C>G maps to NM_002487.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr3:179332846 G>A maps to NM_002492.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:9134276 A>C maps to NM_021074.4 *250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:21074699 C>T maps to ENST00000430741 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:56209011 T>A maps to ENST00000508342 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:29879421 G>A maps to NM_021076.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:24813108 C>T maps to ENST00000221169 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:72058521 G>A maps to NM_173808.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:52676359 C>T maps to NM_199289.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:20940847 T>C maps to NM_006157.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:45169891 G>A maps to NM_001145107.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7219539 C>A maps to NM_032442.2 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:182543458 G>A maps to NM_002500.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:113436534 G>A maps to NM_024019.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr20:50139906 C>T maps to NM_012340.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr16:68200784 T>C maps to NM_173165.2 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:178095659 G>C maps to NM_006164.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:26192150 C>T maps to NM_004289.6 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:31526159 G>A maps to NM_005007.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr9:33295249 C>T maps to NM_002504.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:17710477 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:17750471 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:17746279 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:71358706 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:71359835 C>T did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr14:52521020 G>T maps to NM_007361.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:51210966 G>A maps to NM_020921.3 V1727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr15:23006810 A>G maps to NM_030922.6 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:119070326 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118724927 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118724344 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70375127 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:5821877 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:5811613 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:5821806 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr16:3613452 G>A maps to ENST00000448023 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:32476391 G>A maps to NM_021209.4 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:7060093 G>T maps to NM_176822.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:55497517 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:56538861 C>T maps to NM_153447.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:55450259 C>A maps to ENST00000446217 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr19:56466005 G>A maps to NM_176811.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:56485189 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:56249560 G>A maps to NM_176820.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:119044560 C>T maps to NM_024618.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr5:43675665 A>C maps to NM_182977.2 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:892378 C>T maps to NM_015658.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr12:132633384 G>A maps to NM_024078.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:103921998 C>T maps to ENST00000405356 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr16:14980688 C>T maps to ENST00000456867 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70514335 A>C did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:150698908 C>T maps to NM_000603.4 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr9:139400312 A>T maps to NM_017617.3 C1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:139418328 G>A maps to NM_017617.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:46443288 G>T maps to NM_002516.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100099014 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:34269486 C>T maps to NM_001164749.1 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:34270071 C>T maps to NM_001164749.1 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr11:66191698 C>G maps to NM_178864.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr7:44574198 G>T maps to NM_013389.2 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:53901162 G>T maps to NM_003717.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr5:170819813 T>A maps to NM_002520.6 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:106879673 A>G maps to ENST00000503451 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:153660532 C>A maps to NM_000906.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:35807133 C>T maps to NM_003995.3 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr5:32712484 A>C maps to ENST00000265074 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:98257874 C>T maps to NM_002523.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr4:156135432 G>A maps to NM_000910.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:24018774 A>G maps to NM_005126.4 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:95461144 C>A maps to NM_003297.2 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:92929319 G>A maps to NM_005654.4 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr15:96880649 C>T maps to NM_021005.3 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr4:149356962 A>G maps to ENST00000511528 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr4:149356601 C>A maps to ENST00000511528 G471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:52451180 G>A maps to ENST00000360284 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:102595039 C>T maps to NM_173200.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:200017906 C>T maps to NM_205860.1 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:127302466 C>A did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr9:127300414 G>A maps to NM_033334.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr10:115402733 G>A maps to ENST00000369358 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:115410305 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:115413815 A>G maps to ENST00000369358 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:52258047 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:52271204 C>T maps to NM_002525.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr8:32505334 G>A maps to NM_013959.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:16337986 C>A maps to NM_003489.3 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:16339937 A>G maps to NM_003489.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:105153214 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105179174 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105190309 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105187974 C>A did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr2:50723041 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr11:64453156 G>A maps to NM_015080.3 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:176696630 C>T maps to NM_022455.4 R1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr23:152037349 A>C did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr17:44782177 G>A maps to NM_006178.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:212964985 G>T maps to NM_015471.3 C40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr2:18765800 C>T maps to ENST00000455492 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr11:132180093 A>C maps to NM_001144058.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:96052891 G>T maps to NM_021229.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:49174006 G>A maps to NM_145807.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr9:87635191 G>A maps to NM_006180.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:205290639 C>T maps to ENST00000441520 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:162883964 T>C maps to NM_145266.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:44530145 C>T maps to NM_015332.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:105643363 G>A maps to NM_177533.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:69096537 G>T maps to NM_020401.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:17629399 C>T maps to ENST00000430136 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:135304340 T>C maps to NM_015135.2 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:154098813 G>T maps to NM_207308.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:102468811 G>A maps to NM_024057.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr6:150067547 G>A maps to NM_198887.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:77053688 C>T maps to ENST00000458189 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106396733 C>A did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr16:56792512 G>T maps to NM_014669.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:3781835 C>T maps to NM_016320.4 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr19:16872831 C>T maps to ENST00000438489 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101623765 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:101092526 A>T did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr10:105657467 G>A maps to NM_024928.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:228474714 C>T maps to NM_001098623.1 C3173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:228547519 G>A maps to NM_052843.2 E6309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:228481946 G>A maps to NM_001098623.1 P3742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:220421347 G>A maps to NM_015311.2 A1388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:133036748 G>A maps to ENST00000262283 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr19:17338750 T>C maps to NM_024578.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:128710409 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:128696429 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:123538967 G>A did not map to a codon.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:123838997 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:123519847 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:124097441 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:123554639 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:183714932 G>T maps to NM_001080477.1 E2370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:44739759 C>T maps to ENST00000444676 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr23:70784519 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70757898 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70793482 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:138011984 C>T maps to NM_014279.4 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:9964924 G>A maps to NM_058164.2 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:76813926 G>A maps to NM_006189.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr18:55102968 C>G maps to NM_004852.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr23:67433757 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:67426471 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:67333046 G>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:29189254 C>T maps to NM_000911.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:54163549 G>A maps to NM_000912.3 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr6:154360936 C>T maps to NM_001145279.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr11:7950116 G>A maps to NM_001004461.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr12:55615302 C>T maps to NM_001005280.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr1:159505383 C>T maps to NM_001004469.1 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:159505080 G>A maps to NM_001004469.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:56031268 C>A maps to NM_206899.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:56031001 C>T maps to NM_206899.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:20692491 C>A maps to NM_001004480.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr14:20692035 A>G maps to NM_001004480.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr9:107331462 C>T maps to NM_001004483.1 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:130678386 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:247978587 C>T maps to NM_001001966.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr19:15198439 C>T maps to NM_001004713.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:125424189 C>T maps to ENST00000373686 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr7:143792721 C>T maps to NM_001004135.1 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr1:247614474 G>A maps to NM_001004492.1 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr16:3406725 G>A maps to NM_012368.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:6943084 G>T maps to NM_001004684.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:248113022 C>A maps to NM_001001963.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:248366809 T>C maps to NM_001004689.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:248308943 C>A maps to NM_001004690.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr1:248637451 G>A maps to NM_001005495.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:248637187 C>T maps to NM_001005495.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:248737521 G>A maps to NM_001001821.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:248651993 C>A maps to NM_001004697.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:248059535 C>T maps to NM_001001957.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr11:55110832 T>C maps to NM_001005274.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:48511045 C>A maps to NM_001005512.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr11:48347055 C>A maps to NM_001004702.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr14:20404415 T>C maps to NM_001004063.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr14:20483157 C>T maps to NM_001004712.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr14:20344722 C>A maps to NM_001005501.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:20295870 G>A maps to NM_001004723.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr11:4703776 G>A maps to NM_030774.3 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:4703812 G>T maps to NM_030774.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:5443751 G>T maps to NM_001004757.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:5809139 G>A maps to NM_001001913.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr11:6129436 T>G maps to NM_001005181.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr11:55798809 G>T maps to NM_001001921.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:55541029 C>T maps to NM_001001967.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr11:55563681 C>T maps to NM_001004735.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:55587890 G>T maps to ENST00000395203 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr3:98002238 A>C maps to NM_001005482.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr11:55579556 G>A maps to NM_001004738.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:7817520 C>A maps to NM_153444.1 *323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr11:56043797 C>A maps to NM_001004745.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:56020295 C>A maps to NM_001004747.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:29323300 G>T maps to NM_030876.5 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:143701691 C>A maps to NM_001005281.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:55688183 G>T maps to NM_001005493.1 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:55863897 C>A maps to NM_001005499.1 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:247875277 G>A maps to NM_001005286.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:158670013 C>A maps to NM_001005279.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:142749857 C>T maps to NM_001001667.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:9213577 G>T maps to NM_001005193.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:124440833 C>T maps to NM_001005194.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:55890693 T>C maps to NM_001005201.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:55861061 C>A maps to NM_001003750.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:56468603 C>A maps to NM_001013358.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:21819301 G>T maps to NM_080597.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr2:179213991 C>A maps to ENST00000392505 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:190936631 G>T maps to NM_198184.1 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:146058847 C>A maps to ENST00000447906 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:92082633 G>T maps to NM_016023.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:97639791 G>A maps to NM_080818.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:8809318 G>A maps to NM_000916.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:57114098 C>T maps to NM_002559.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr22:21377576 G>T maps to NM_005446.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:121570868 C>T maps to NM_002562.5 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:78216917 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:78216974 G>T did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr23:78216442 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1584446 G>A did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr23:90690675 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:90691337 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:90690888 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:17570623 C>T maps to NM_013358.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:55102523 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:28862174 C>A maps to NM_175854.7 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:124489662 C>A maps to NM_052959.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:176525514 C>G maps to NM_020318.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:176709278 G>A maps to NM_020318.2 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:79845023 C>T maps to NM_001040202.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr5:50045993 C>A maps to ENST00000505697 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr3:122247219 A>T maps to NM_031458.2 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:150840934 A>C did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr2:242062239 G>A maps to ENST00000358649 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:242078092 C>T maps to ENST00000358649 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:242079938 T>G maps to ENST00000358649 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:19018401 C>T maps to NM_002584.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:70045060 C>T maps to NM_001033083.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:52643767 G>A maps to ENST00000296302 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:91090728 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:91133601 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:55955447 C>A maps to NM_001142763.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:55626541 C>A maps to NM_001142763.1 E1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:99662931 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:99657836 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:61987060 G>A maps to NM_022843.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr5:140237390 G>A maps to NM_018901.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140249077 G>A maps to NM_018902.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr5:140176606 C>T maps to NM_018905.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140188073 G>A maps to NM_018907.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr5:140209478 A>G maps to NM_018909.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr5:140215890 C>T maps to NM_018910.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140215941 G>A maps to NM_018910.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:140229831 G>A maps to NM_031857.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140229594 G>A maps to NM_031857.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr5:140573706 G>T maps to NM_018930.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:140564302 C>T maps to NM_020957.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:140515027 G>A maps to NM_015669.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr5:140516677 C>T maps to NM_015669.2 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr5:140793311 C>T maps to NM_018913.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140720037 C>T maps to NM_018915.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:140764736 C>G maps to NM_018920.2 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140773528 C>A maps to NM_032088.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr5:140751622 C>T maps to NM_018924.2 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:140858061 T>C maps to NM_002588.2 D793D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:120388229 C>T maps to NM_001029996.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:82764633 C>T maps to NM_033026.5 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr7:82584376 C>T maps to NM_033026.5 T1964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:52773450 C>A maps to NM_052937.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:71478245 C>T maps to NM_014982.2 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:95751802 C>A maps to NM_000439.4 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:117090318 G>A maps to NM_004716.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:55527144 G>A maps to NM_174936.3 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr3:195974348 C>T maps to NM_005017.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:186415579 G>T maps to ENST00000340129 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:167414851 G>A maps to NM_145859.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:105158248 T>G maps to NM_014976.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr19:33077793 A>T maps to NM_004708.3 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:144931279 C>T maps to NM_001002811.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:85664053 C>T maps to NM_002605.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:76645303 G>T maps to NM_003719.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:44152235 T>C did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:149497299 G>A maps to NM_002609.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr15:44048890 C>T maps to NM_005313.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr7:148718138 T>C maps to NM_004911.4 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:24549845 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:33316751 T>C maps to ENST00000400481 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:27012968 G>T maps to NM_014317.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:69507612 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:32088776 C>T maps to NM_178140.2 D1741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:41967014 G>T maps to NM_001164595.1 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:94292898 G>A maps to NM_001172437.1 *86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:57327757 G>A maps to NM_006210.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:57326133 G>A maps to NM_006210.2 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:66239871 G>A maps to NM_145065.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:33904941 C>T maps to NM_000286.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:54978378 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:149684299 T>C maps to NM_053024.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr23:77224930 T>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr2:197707533 A>C maps to NM_024989.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:97978233 C>A maps to ENST00000325141 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr17:76395555 C>T maps to NM_024419.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr6:144093532 C>T maps to NM_001100164.1 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:169846642 C>T maps to NM_024947.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:46913858 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:64394336 T>C maps to NM_015153.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:133527537 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:71802318 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr23:18972447 A>C did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr23:18929041 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:111671465 C>A maps to NM_001134438.1 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:71701132 G>A maps to NM_015020.2 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:170557639 G>A maps to NM_001008489.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:61004993 A>G maps to NM_032439.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:21081547 G>A maps to NM_058004.2 Y1579Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr13:73357693 T>C maps to NM_006346.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:15349744 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:15344080 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:172411564 A>G maps to NM_153747.1 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr4:517576 C>A maps to NM_001127178.1 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:207110845 G>A maps to NM_002644.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:204438066 G>T maps to NM_002646.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:18435081 G>T maps to NM_004570.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:106508092 G>A maps to NM_002649.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr1:151205103 C>T maps to NM_001135638.1 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:71491649 C>T maps to NM_003558.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:71491677 G>T maps to NM_003558.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:3656426 C>T maps to NM_012398.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:94310615 C>T maps to NM_152431.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:68381327 T>C did not map to a codon.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr23:68382932 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:81193408 C>T maps to NM_052892.3 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr16:81197273 G>A maps to NM_052892.3 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr10:102054718 A>G maps to NM_016112.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr6:51889955 G>T maps to NM_138694.3 S1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:110504168 A>G maps to ENST00000426474 G3394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr15:72492886 G>A maps to ENST00000419739 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr11:125301239 G>A maps to NM_022062.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr15:42374008 G>C maps to NM_178034.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr2:160807931 T>C maps to NM_007366.4 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr23:133700505 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:59811080 G>A maps to NM_173801.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr20:9343592 C>T maps to NM_001172646.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:38050772 G>A maps to NM_001130964.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:96030303 C>A maps to ENST00000371380 S1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:39800864 G>A maps to NM_002660.2 K947K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:155206446 A>G did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:215881 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:215972 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:41313763 G>T maps to NM_001005473.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:144994412 G>T maps to NM_201380.2 Y3329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:68622923 G>A maps to NM_002664.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:151153216 G>A maps to NM_001029884.1 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:155040 C>T maps to NM_052909.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:6427544 C>T maps to NM_001144856.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:2233839 C>T maps to NM_018049.1 *150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr19:4859937 G>A maps to NM_005817.4 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:103040583 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:103040635 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:103040658 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:49029576 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:114856632 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:31830329 C>A maps to NM_130852.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:153692520 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153697245 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153692556 G>A did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:153039478 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:57569888 C>T maps to ENST00000269518 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:152936420 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:118355760 C>A maps to NM_006229.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:152226672 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:152226401 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:152226513 C>A did not map to a codon.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr23:152159975 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:152159546 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:140354850 G>A maps to NM_001098537.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:46022056 C>T maps to NM_018129.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:84601020 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:84563197 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:133225984 G>A maps to ENST00000455752 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:51810357 G>T maps to NM_007195.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:2210082 T>G maps to NM_181808.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:121190984 T>C maps to ENST00000393672 L2326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:121260218 T>A maps to ENST00000393672 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:86274380 G>T maps to NM_015425.3 C880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7404317 G>A maps to NM_000937.4 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr8:22106725 C>G maps to NM_001722.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr9:134379640 G>C maps to NM_007171.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:134382767 C>T maps to NM_007171.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr9:134385762 C>T maps to NM_007171.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr18:14543049 G>A maps to ENST00000444806 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr21:14982926 C>T maps to NM_174981.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr2:130832626 G>A maps to NM_001099771.2 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:120139926 C>T maps to NM_014352.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:99283718 C>T maps to NM_005604.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:82763426 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:82764036 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:46627933 C>T maps to NM_001001928.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:23815614 T>C maps to NM_013261.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:70170512 C>T maps to NM_003626.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:81741355 G>A maps to NM_003625.2 R730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:81777836 C>A maps to NM_003625.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:7663586 C>T maps to NM_003621.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:40207069 G>T maps to NM_006112.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr2:170494026 C>T maps to NM_004792.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr16:4949274 G>A maps to NM_002705.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr17:57057476 C>T maps to NM_014906.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:63182118 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:204379609 C>T maps to NM_032833.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:37546948 T>C maps to NM_015568.2 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:37547185 G>A maps to NM_015568.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr7:113518496 G>A maps to NM_002711.3 Q884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:49142812 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:146077607 C>A maps to ENST00000394414 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:133758847 C>A maps to ENST00000455566 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:135722019 C>A maps to NM_002718.4 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:104357194 G>A maps to NM_147180.2 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:103900433 C>A maps to NM_015062.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:103901270 G>A maps to NM_015062.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:47087544 C>T maps to NM_005972.4 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:48929637 G>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr19:8555520 G>A maps to NM_032152.4 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr1:13716935 G>A maps to NM_001099851.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:82564262 G>A maps to NM_199418.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:108145726 A>C maps to NM_012406.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr4:81123236 C>T maps to NM_001099403.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr5:23526780 G>A maps to NM_020227.2 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:72360547 G>A maps to NM_005041.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:64084735 G>T maps to NM_198859.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:49032105 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:49032094 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:49033340 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:49032045 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:57183335 G>A maps to NM_000947.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:47204174 C>T maps to ENST00000449438 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr6:22290510 C>T maps to ENST00000397199 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:35084593 A>C maps to NM_000949.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:4705394 C>T maps to NM_012409.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr2:95954316 T>C maps to NM_144707.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:93605178 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:214171527 C>A maps to NM_002763.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:109242060 C>T maps to NM_018061.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:1563259 C>T maps to NM_006445.3 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:42689571 G>T maps to NM_000322.4 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:855732 G>A maps to NM_001013638.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:170633454 G>A maps to NM_022716.2 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr6:84234377 C>T maps to NM_153362.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:31143830 G>A maps to NM_002773.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:55912374 A>G maps to NM_173814.4 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:79520870 T>C maps to NM_015225.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:43411077 G>T maps to NM_002782.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:14535161 T>C maps to NM_148976.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107331315 G>T did not map to a codon.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr18:12725486 G>A maps to NM_020232.4 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:97235319 T>C maps to ENST00000370197 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:97217024 G>A maps to ENST00000370197 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:98238410 C>A maps to NM_000264.3 G545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:98244435 C>A maps to NM_000264.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:23397856 T>C did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:11589624 C>T maps to NM_020780.1 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:11589955 C>G maps to NM_020780.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr10:89720876 T>G did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:89711982 G>T maps to NM_000314.4 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr5:40691916 T>C maps to NM_000958.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:117491979 G>A maps to NM_020440.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:87696406 T>A maps to NM_080685.2 V1869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:87724874 G>C maps to NM_080685.2 L2178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:87622928 T>C maps to NM_080685.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr3:47451556 C>T maps to NM_015466.2 R757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr11:18755101 C>T did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr12:70963617 C>A maps to NM_001109754.1 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:198682091 G>A maps to ENST00000271610 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr9:8331733 G>A maps to NM_002839.3 D1794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:8404576 G>A maps to NM_002839.3 I1390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:44075092 G>C maps to NM_002840.3 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:44057542 C>A maps to NM_002840.3 S531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr3:62259444 C>T maps to NM_002841.3 Q1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:62188854 G>A maps to NM_002841.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr18:8380346 A>C maps to NM_001105244.1 T1280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:8143717 C>T maps to NM_001105244.1 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:40827895 C>T maps to ENST00000373198 Q847Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr17:40557061 C>T maps to NM_012232.5 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr12:44124454 T>C maps to NM_031292.3 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:52336135 C>A maps to NM_144651.4 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:52287291 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr12:120652777 C>T maps to NM_001080855.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:36359627 A>G maps to NM_152990.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr20:25277118 C>T maps to NM_002862.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:158909027 C>T maps to NM_152501.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:21615023 A>G maps to NM_024854.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:119798540 C>A maps to ENST00000369199 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:27826848 G>T maps to NM_021252.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:82698746 G>A maps to NM_014488.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr23:129306072 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:154490294 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:70149247 G>A maps to NM_175623.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:80617461 G>A maps to NM_006822.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:6441992 C>T maps to NM_018890.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr8:95403997 G>A maps to NM_012415.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr6:150210551 G>T maps to NM_139165.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:121043520 T>G maps to NM_002881.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:36155764 G>A maps to NM_194301.2 R848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:36096693 G>A maps to NM_194301.2 C1647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:85774638 C>T maps to NM_001100391.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:41654016 G>A maps to NM_002883.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:173866009 C>T maps to NM_007023.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:86668013 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:85611949 G>A maps to NM_152573.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:79294115 G>T maps to NM_002891.4 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr15:38811526 C>T maps to NM_005739.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr19:49228097 G>A maps to NM_017805.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:27847484 G>T maps to NM_206827.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr13:48881413 A>G did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:48955516 G>T maps to NM_000321.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:48937069 G>T maps to NM_000321.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr13:48916758 G>T maps to NM_000321.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:24560269 C>T maps to NM_006910.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr23:16870878 G>A did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:18477787 C>T maps to NM_006606.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:114364908 G>A maps to NM_016196.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr7:127958087 C>T maps to NM_018077.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:106332029 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:152107613 C>A maps to NM_198557.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:135960090 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135961189 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129545331 G>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:173907981 T>C maps to NM_172071.2 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:173962047 G>A maps to NM_172071.2 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:110134818 T>C maps to ENST00000405097 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr17:73661199 G>A maps to NM_004259.5 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:112238186 C>A maps to NM_005669.4 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153207460 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:17153396 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:15262228 C>A maps to NM_032918.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:85577955 C>A maps to NM_017750.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:111680168 G>A maps to NM_002912.3 R2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr19:1828424 G>A maps to NM_020695.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:39304133 G>A maps to ENST00000381897 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:118467595 C>T maps to NM_007370.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:32754064 A>C maps to NM_001098535.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:112671558 G>T maps to NM_001013734.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr19:14090341 G>A maps to NM_002918.4 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:109694815 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:109695279 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:109694333 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr23:71350556 T>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:71350290 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:73181708 G>A maps to NM_001080479.2 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:3318235 C>T maps to NM_198229.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:54791867 C>T maps to NM_170587.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:101117606 C>A maps to NM_015668.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:116356772 T>C maps to NM_144488.4 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:241094032 C>T maps to ENST00000407727 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:74469405 A>G maps to NM_024599.5 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:39358896 C>A did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:119249404 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:119249748 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr2:152321301 C>T maps to NM_018151.4 D1756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:152273331 A>C maps to NM_018151.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:42875736 C>T maps to NM_173642.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:72945356 C>T maps to NM_014989.4 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:19956198 G>A maps to ENST00000255006 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:24808483 C>A maps to NM_006871.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106146381 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:40701802 C>T maps to NM_012421.3 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr23:73811852 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:73811354 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:67681791 C>T maps to NM_001013838.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr14:21423972 C>T maps to NM_002934.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr13:98829046 C>T maps to NM_178861.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:71693850 A>C maps to NM_018320.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:106034390 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr23:105937563 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106038843 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:179394007 C>T maps to NM_018434.4 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:125499513 G>T maps to NM_007218.3 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:44036490 C>A maps to NM_152470.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:20141294 G>A maps to NM_019062.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:104316368 G>A maps to NM_019592.5 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:79213181 C>A maps to NM_024546.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr18:13741540 A>G maps to NM_003799.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr3:77595593 G>A maps to ENST00000332191 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:11337449 G>A maps to NM_004850.3 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:64605807 T>C maps to NM_005012.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:77275551 C>A maps to ENST00000396204 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:117609890 C>A maps to NM_002944.2 E2270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr6:117686851 T>A maps to NM_002944.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:55541338 G>T maps to NM_006269.1 E1633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr8:10470755 C>T maps to NM_178857.5 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:96139444 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:21793212 C>T maps to NM_020366.3 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr13:27827918 G>A maps to NM_000982.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr16:1995898 G>A maps to NM_005061.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr12:120637129 G>A maps to NM_053275.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:149826513 G>A maps to NM_005617.3 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr23:20185862 T>C did not map to a codon.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr23:83403057 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:83359666 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:213414613 G>T maps to NM_012424.3 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:9883746 C>T maps to NM_173659.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:55757848 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:45107838 A>G maps to NM_015056.2 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr23:18660258 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:7030404 C>T maps to NM_080657.4 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr7:77378906 A>G maps to NM_198467.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:15987115 C>T maps to NM_006511.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:116949484 G>T maps to NM_001010892.2 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:63957809 G>A maps to NM_145307.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:1840608 G>A maps to NM_178568.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:187089080 C>T maps to NM_022147.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:42392101 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:36259340 G>C maps to NM_001754.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:30380934 G>A maps to NM_016940.2 Y25Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:32351560 G>A maps to NM_130806.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:33937051 C>T maps to NM_016568.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr19:38976496 C>T maps to NM_000540.2 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:38990407 C>T maps to NM_000540.2 S2387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:237957189 A>G maps to NM_001035.2 R4602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:237870480 G>A maps to NM_001035.2 E3271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:237961429 G>T maps to NM_001035.2 E4684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:237604645 G>T maps to NM_001035.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr15:34018591 C>A maps to NM_001036.3 I2306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:34080593 C>T maps to NM_001036.3 F3255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:34049794 C>T maps to NM_001036.3 A2901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:34040341 C>T maps to NM_001036.3 R2673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:153591515 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:101705190 C>T maps to NM_001400.4 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:23914021 A>G maps to NM_014363.4 H1331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:23932557 C>A maps to NM_014363.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134991920 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134995040 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr18:76754279 C>T maps to NM_171999.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:76754411 C>T maps to NM_171999.2 D807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:55168870 C>T maps to NM_015589.4 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr19:39869207 C>T maps to NM_018028.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:92765170 G>A maps to NM_152703.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr2:128757878 A>C did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr11:65729346 C>T maps to NM_005146.4 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:100575955 T>C maps to NM_194292.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr14:51101950 G>A maps to NM_021818.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr19:50154614 C>T maps to NM_021228.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:1918132 C>T maps to NM_079834.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:28543363 G>T maps to NM_052923.1 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:77091019 A>C maps to NM_005506.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:35085453 G>A maps to NM_001025591.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:41541091 G>A maps to NM_001031694.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr23:17770058 C>T did not map to a codon.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:18338511 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:18260637 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr3:38798314 T>G maps to NM_006514.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:38991630 C>A maps to ENST00000302328 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:166908388 C>T maps to NM_001165963.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:166897797 G>T maps to NM_001165963.1 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:166165695 C>T maps to NM_001040143.1 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr2:165969451 A>T maps to NM_006922.3 Y1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:62034758 G>A maps to NM_000334.4 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:52183108 C>A maps to NM_014191.2 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:52115649 C>T maps to NM_014191.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr16:23366759 C>G maps to ENST00000307331 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr8:144885554 C>A maps to NM_182706.3 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:175265747 A>G maps to NM_024583.4 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr11:65302777 C>T maps to NM_020680.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:100709496 G>A maps to NM_017988.4 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:31347423 T>C maps to NM_014654.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:1152960 G>C maps to NM_016176.3 L340L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ND-A4WC-01A-21D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:251453 A>G maps to NM_004168.2 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr17:71344824 C>G maps to NM_001144952.1 S2026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr14:39556160 G>A maps to NM_006364.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:110384777 G>A maps to NM_006323.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr4:110384636 G>A maps to NM_006323.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:83788041 C>T maps to ENST00000505472 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:127785898 C>T maps to ENST00000464451 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:83823878 G>A maps to NM_006080.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr7:84628908 G>A maps to NM_152754.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr5:9043071 A>G maps to NM_003966.2 H1054H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:115783142 C>T maps to ENST00000257414 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:48052093 C>T maps to NM_153618.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:48468233 G>T maps to ENST00000004980 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:196650378 C>A maps to NM_152699.4 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:13375826 C>A maps to NM_012247.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:55873083 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:56604288 G>A maps to NM_004574.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118763352 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr17:75471731 G>A maps to NM_001113495.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:42968532 G>T maps to NM_014509.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr14:94770859 C>T maps to NM_001756.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:105280575 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr18:61468143 C>T maps to NM_001040147.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr18:61449728 G>T maps to NM_001040147.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr18:61654203 C>T maps to NM_198833.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr6:2893764 C>T maps to NM_004155.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:167185067 C>A maps to NM_006217.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:198274671 G>A maps to NM_012433.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr16:70575649 A>G maps to NM_012426.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:7242374 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:22019364 C>T maps to NM_003018.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:120907362 C>A maps to NM_213649.1 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:23853607 C>T maps to NM_000231.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr1:67148014 C>T maps to ENST00000237247 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr6:134491531 G>C maps to NM_001143676.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:52066984 G>A maps to ENST00000361543 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:111886102 C>A maps to NM_005475.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:235951497 C>T maps to NM_014521.2 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19725021 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:19560161 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:171849419 C>T maps to NM_001017995.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:218857 G>A maps to NM_015677.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr11:70505947 C>G maps to ENST00000338508 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:201860580 C>A maps to NM_198149.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr23:601570 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:9862499 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:77700185 C>A maps to NM_020859.3 V1949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:50351175 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:50339754 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:50377888 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr21:44840173 G>A maps to NM_173354.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:111583041 A>G maps to NM_015191.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr5:138282943 G>C maps to ENST00000509534 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr5:138456751 C>T maps to ENST00000509534 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:100896034 G>A maps to ENST00000262901 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:100838344 G>T maps to ENST00000262901 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr15:75684735 G>A maps to NM_001145357.1 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:38633332 C>G maps to NM_015073.1 Y1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:54640966 C>T maps to NM_015360.4 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr13:103698524 C>T maps to NM_000452.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:153716853 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr4:147204389 G>A maps to ENST00000507030 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:1075523 G>A maps to NM_006598.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:1057650 G>A maps to NM_006598.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:60718780 G>A maps to NM_016582.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:111409146 C>T maps to NM_018593.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:111540114 C>T maps to NM_018593.4 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr17:6946802 A>G maps to NM_153357.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr10:91198854 G>A maps to NM_213606.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:73744510 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:73740967 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096693 C>G maps to ENST00000450736 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096219 C>T maps to ENST00000450736 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096838 C>T maps to ENST00000450736 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096513 C>T maps to ENST00000450736 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:60098717 G>T maps to NM_004731.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr6:74363525 C>A maps to NM_012434.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr11:22396404 G>A maps to NM_020346.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr10:119027212 C>A maps to NM_003054.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:119003728 C>T maps to NM_003054.4 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:62996980 G>A maps to NM_199352.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:19786015 G>A maps to NM_020344.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:92958060 C>T maps to NM_153646.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:95813663 C>A maps to NM_001160210.1 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:95813702 G>A maps to NM_001160210.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr6:46623608 C>T maps to NM_004277.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr12:98987869 C>G maps to NM_213611.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr17:42398462 G>A maps to NM_001143780.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118603828 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:1506217 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:149360082 T>G maps to NM_000112.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:107417135 C>T maps to NM_000111.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr8:92346558 C>A maps to NM_134266.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:128362946 C>G maps to NM_001017372.1 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:45362451 C>T maps to NM_030777.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:48762194 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:44224542 C>A maps to NM_178148.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:31042915 C>T maps to NM_001001479.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:118228912 G>A maps to NM_001029858.3 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:118475688 A>G maps to NM_001029858.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:118556697 C>T maps to NM_001029858.3 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:92901247 C>T maps to NM_152313.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:50255383 C>T maps to NM_006841.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:48317962 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:54931419 A>C maps to NM_173514.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr2:196573522 C>T maps to NM_001127257.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:105282850 A>G maps to NM_032148.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:74491272 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:74458401 G>T maps to NM_021196.3 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr3:27475587 T>A maps to ENST00000454389 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:17986846 C>A maps to NM_000453.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:27423871 G>A maps to NM_021095.2 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr12:101561909 G>A maps to NM_145913.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:10970991 C>A maps to NM_014229.1 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:115574870 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:115590114 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:85285787 C>A maps to NM_182767.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:55733484 C>T maps to NM_001043.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:45817309 G>A maps to NM_020208.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:1420692 G>A maps to NM_001044.4 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr5:1420692 G>A maps to NM_001044.4 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:152960289 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:44474143 G>A maps to NM_201649.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:139101829 G>A maps to ENST00000280612 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr8:87229899 T>G maps to NM_138817.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:70148384 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:70147404 C>T did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr2:40656142 G>A maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:40342515 G>A maps to NM_021097.2 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:40401858 T>C maps to NM_021097.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:40366763 G>A maps to NM_021097.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr19:47935655 C>T maps to NM_015063.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:476345 G>A maps to NM_004174.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:135104831 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:143082375 C>T maps to NM_173653.3 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:21294588 G>A maps to NM_006446.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:21028324 C>A maps to NM_019844.2 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:20905331 C>G maps to NM_017435.4 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:133664064 G>T maps to NM_005630.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:133661612 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:101576466 G>T maps to NM_180991.4 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:101583038 T>C maps to NM_180991.4 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:33690360 T>G maps to NM_152270.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:168180966 G>A maps to NM_003062.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr23:144906236 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:144906075 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:59179666 G>A maps to NM_024755.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr6:71501408 T>A maps to NM_001044305.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:128657269 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:128599821 T>G did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:2191348 C>T maps to NM_003070.3 R1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr4:144445585 C>T maps to NM_003601.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:95201892 C>T maps to NM_001128429.1 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:95200128 C>T maps to NM_001128429.1 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:56568508 T>G maps to NM_003075.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:56566437 C>T maps to NM_003075.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr23:53432008 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr23:53432288 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:112361579 C>T maps to NM_005445.3 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:18823417 C>T maps to ENST00000389467 Q3552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:156222290 G>A maps to NM_015327.2 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:22003282 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:33053231 G>A maps to NM_018225.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:1703307 C>T maps to NM_052928.2 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:127721474 C>T maps to NM_014390.2 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:127721494 C>T maps to NM_014390.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:1285530 G>A maps to ENST00000381876 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:101832241 A>G maps to NM_003090.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:122281827 C>T maps to ENST00000395451 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr4:186263242 T>C maps to NM_031953.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:151611415 C>T maps to ENST00000458013 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:179320590 G>A maps to NM_003101.4 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:34948144 A>G maps to NM_138927.1 E2389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:186535982 A>G did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:108366949 T>A maps to NM_001013031.1 K1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:108412180 C>A maps to NM_001013031.1 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:7725500 C>T maps to NM_020777.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr10:107015548 G>A maps to NM_014978.1 Q1109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:121393332 C>T maps to NM_003105.5 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:139586342 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:157053527 A>G maps to NM_178424.1 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:70120194 G>A maps to NM_000346.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:53722253 G>A maps to NM_001173467.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:53722394 C>T maps to NM_001173467.1 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:118629492 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:144337198 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:144337189 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:142605154 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:151052737 C>A maps to NM_003118.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:24860368 C>T maps to ENST00000424834 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:177114179 T>C maps to NM_144644.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr4:123855465 G>T maps to NM_145207.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:123949433 C>T maps to NM_145207.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:88892856 G>A maps to NM_018418.4 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:35763638 T>C maps to NM_024867.3 P1212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:69238253 C>T maps to NM_145658.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr2:228882545 G>A maps to NM_001142644.1 D1008D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:228884216 G>A maps to NM_001142644.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:101873372 C>A maps to ENST00000299272 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr16:89922601 C>A maps to NM_032451.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:153012693 C>T maps to NM_006945.4 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:6981729 G>T maps to NM_032641.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:158618427 C>T maps to NM_003126.2 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:41072111 T>C maps to NM_020971.2 D2061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:42162109 G>A maps to ENST00000320955 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr5:179263547 G>A maps to NM_003900.4 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr17:36707583 G>T maps to NM_025248.2 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:56230295 C>T maps to NM_024592.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr22:42299023 C>T maps to NM_004599.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:42273339 T>G maps to NM_004599.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:121355980 C>A maps to NM_152546.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:74046598 G>A maps to NM_014230.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:99922391 C>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:99917214 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:119583268 C>T maps to NM_194286.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr20:60736499 G>A maps to NM_198935.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:153063543 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:38678968 C>T maps to NM_001049.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr20:23016959 G>C maps to NM_001052.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:1129539 C>T maps to NM_001053.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48125775 T>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:48047158 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48054554 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr23:52677446 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:52681945 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:104122664 T>A maps to NM_017564.9 V1658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:104134517 C>T maps to NM_017564.9 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:57642497 G>A maps to NM_145064.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:136323150 C>T maps to NM_005862.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:136221538 G>A maps to NM_005862.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:123185194 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:99798885 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:96858112 A>G maps to NM_020151.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:67943866 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:191844514 G>T maps to NM_007315.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:87913197 G>A maps to NM_024636.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:47728787 G>A maps to NM_001048166.1 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:27003939 G>T maps to ENST00000382009 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:171509416 G>A maps to NM_005990.3 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:23871983 A>C maps to NM_031414.3 *1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:70641819 A>G maps to NM_001130161.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:37121136 G>A maps to NM_003162.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:70512900 A>G maps to NM_001128206.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:108921631 T>G maps to ENST00000437390 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr2:108868908 C>T maps to NM_001008743.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr7:56140698 C>G maps to ENST00000395437 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:21828671 G>A maps to NM_007192.3 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:39962346 C>T maps to NM_003169.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:70946298 C>T maps to NM_003171.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:48558920 A>C did not map to a codon.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr10:14939227 T>C maps to NM_001193424.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr17:30293183 G>A maps to NM_015355.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr15:91795209 C>T maps to NM_014848.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:29769556 G>A maps to NM_021738.2 F1762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:29843733 G>A maps to NM_021738.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr8:110590122 C>T maps to NM_001099744.1 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:13015377 G>A maps to NM_001105578.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:102122936 C>A maps to ENST00000449403 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:85656052 A>G maps to NM_032184.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:46332274 G>A maps to NM_004819.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:152673365 A>G maps to NM_182961.2 D3792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr16:2042102 C>G maps to NM_004209.5 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr21:34053868 G>A maps to NM_003895.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:99672120 G>T maps to ENST00000336292 E1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:119978689 A>C maps to NM_133477.2 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:119952572 G>A maps to NM_133477.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:79679636 C>A maps to NM_005639.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:46964008 G>C maps to NM_031912.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:37893259 A>T did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:132910255 G>T maps to NM_003967.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:30872876 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:30872824 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr10:123810032 G>T maps to NM_206862.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1729656 C>T maps to NM_006342.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr23:70607150 A>G did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr23:70607292 T>C did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr23:70621555 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:8007599 G>A maps to NM_031923.2 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:8007252 G>T maps to NM_031923.2 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:62549790 C>G maps to NM_006473.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr23:100531441 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100530219 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:100532612 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:42036323 C>T maps to NM_138572.2 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:118675942 G>A maps to NM_016281.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:33467053 C>T maps to ENST00000455217 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:150478147 C>A maps to NM_025150.3 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr5:9630015 C>T maps to NM_019599.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr7:143175363 C>G maps to NM_176883.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:11139430 G>T maps to NM_176890.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:10959315 G>A maps to NM_023918.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:13463938 G>C maps to NM_017714.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:153649044 G>C did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:96162513 G>A maps to NM_015188.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:47287218 G>T maps to NM_014346.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr23:48418347 C>A did not map to a codon.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr13:75884162 T>C maps to ENST00000431480 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106093367 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106116960 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:106083349 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr11:120925928 C>A maps to NM_152715.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:67400484 C>T maps to NM_005995.4 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:59560406 G>T maps to ENST00000393853 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:114832640 C>A maps to NM_000192.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr7:139715630 G>A maps to NM_001166253.1 W492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:23743806 A>T maps to NM_003196.1 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:102529346 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:57555430 C>A maps to NM_207036.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr20:590482 C>T maps to NM_004609.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:42607448 G>C maps to NM_005650.1 S1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr10:114919685 C>T maps to NM_030756.4 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:114912120 G>A maps to NM_030756.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:152057987 G>A maps to NM_001008536.1 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:59620702 G>A maps to NM_001062.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:111064169 C>T maps to NM_001082538.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:104373822 T>A maps to NM_003211.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:154493951 G>A maps to NM_001098475.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:46659192 G>T maps to NM_001010870.2 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:49845738 G>A maps to NM_003598.1 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:48139467 C>A maps to NM_003215.2 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:97846803 G>A maps to ENST00000379795 D1134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:121008214 C>T maps to NM_005422.2 C1009C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:95537620 C>T maps to NM_144705.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:70405908 A>G maps to NM_030625.2 K1141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:106158561 T>C maps to NM_017628.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:69890344 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107224488 G>T did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:107225157 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:56682458 G>A maps to ENST00000240361 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:62291463 G>A maps to NM_018469.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr10:60154713 C>T maps to NM_003201.1 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr23:132351647 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48891262 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:133923761 T>C maps to NM_003235.4 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:133900319 C>T maps to NM_003235.4 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:135383084 C>T maps to NM_000358.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr1:92178080 C>A maps to NM_003243.4 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:44955153 C>A maps to NM_003241.3 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:2377167 G>T maps to NM_198994.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr20:57564965 C>T maps to NM_198976.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr1:6692464 G>A maps to NM_001195753.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:36526380 G>T maps to NM_152658.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:83839056 A>G maps to NM_024672.4 Q564Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr6:169626325 G>A maps to NM_003247.2 D829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:169629696 G>A maps to NM_003247.2 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr2:137917825 G>A maps to ENST00000272643 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr21:32513670 C>T maps to NM_003253.2 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:155458505 C>T maps to ENST00000456144 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:155569224 G>A maps to ENST00000456144 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr1:43772664 G>T maps to NM_005424.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47444651 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr14:24709662 C>T maps to NM_001099274.1 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:82191077 G>T maps to ENST00000376537 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:120475078 G>T maps to NM_138554.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr23:12903968 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:12938498 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr20:2597823 G>T maps to NM_080751.2 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:68914500 G>T maps to NM_024562.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:102272783 G>T maps to NM_052932.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:98457842 G>C maps to NM_001134450.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr11:60694715 G>A maps to NM_017870.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:129558970 C>A maps to NM_133448.2 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr17:32963036 G>A maps to NM_207313.1 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:48848476 C>T maps to NM_018273.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr4:159140503 G>A maps to NM_018342.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:5766115 G>A maps to NM_152784.3 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:36231465 C>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:109414703 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:150490214 C>T maps to NM_014020.3 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:120438731 G>T maps to NM_030577.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:9661176 C>T maps to NM_001130924.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:136574279 C>A maps to NM_025246.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:102968692 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:25783142 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:44117684 T>C maps to NM_018426.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:205053391 C>G maps to NM_203376.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:69093747 T>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:154741449 T>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:117779387 G>A maps to ENST00000413475 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:19775931 G>T maps to NM_002772.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:117969703 C>G maps to NM_019894.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr3:111797604 C>T maps to ENST00000443106 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr23:103219161 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:29659798 G>A maps to NM_001193451.1 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr13:101266663 G>A maps to NM_032813.2 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:101258624 G>T maps to NM_032813.2 Y707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:57506208 C>A maps to NM_015959.3 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:23049431 G>A maps to NM_003844.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:108922411 C>T maps to NM_006573.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:173155897 G>A maps to NM_003326.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr11:57076215 G>C maps to NM_033396.2 T1323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr23:99852507 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:99852523 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:24834299 G>T maps to NM_014494.2 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:25661351 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:179869291 C>T maps to ENST00000398836 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr17:7578290 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr17:7578555 T>G did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:7579388 G>A maps to NM_001126112.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr17:7579590 C>G did not map to a codon.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr17:7573981 C>A maps to NM_001126112.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr11:68854002 C>T maps to NM_139075.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:18057673 G>A maps to ENST00000341556 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:1457505 C>T maps to NM_000547.5 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:103299591 A>G maps to ENST00000376052 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:140093882 C>T maps to NM_001128228.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr21:10969072 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr21:10921995 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:10920136 G>A maps to NM_199261.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:10908880 G>T maps to NM_199261.2 Y488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:185643395 G>A maps to NM_004593.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr16:67189312 C>T maps to NM_003789.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:36511924 G>A maps to NM_145803.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:202263031 G>A maps to NM_015049.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:71495555 G>T maps to NM_014294.5 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:36874296 T>G maps to NM_014831.2 T2215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:36897167 C>A maps to NM_014831.2 E1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:36873393 C>T maps to NM_014831.2 E2516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:140922402 G>A maps to NM_031466.5 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:17195592 C>A maps to NM_004412.5 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr6:41165845 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:152710334 C>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:72666575 C>T maps to NM_013381.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:72771852 G>T maps to NM_013381.2 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:64907455 C>A maps to NM_001656.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:6478960 C>T maps to NM_033278.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:114964081 C>T maps to NM_015906.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:5699532 C>T maps to NM_033034.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:67064643 G>T maps to NM_184085.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr4:189022257 C>T maps to ENST00000326754 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:189022277 C>A maps to ENST00000326754 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr2:230667107 A>G maps to ENST00000389044 C995C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr23:100278580 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:61444312 T>C maps to NM_020810.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr23:54948701 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr23:54955688 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:54953057 G>T did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr23:54955076 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:142503721 C>A maps to ENST00000476941 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:111078179 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:111019916 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:111019749 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:31323321 G>A maps to NM_002420.4 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:49671541 G>T maps to NM_017636.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:77415319 C>G maps to NM_017662.4 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr2:234847658 C>A maps to NM_024080.4 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:110234488 C>T maps to NM_021625.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:98530910 G>A maps to ENST00000359863 Q1300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:98609881 C>T maps to ENST00000359863 F3828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:107018441 G>A did not map to a codon.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr3:12531436 C>T maps to NM_025265.3 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:12571275 C>T maps to NM_025265.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:130356586 G>C maps to NM_052933.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:31769641 G>A maps to NM_020856.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:98289207 T>G maps to NM_033512.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr17:2228661 C>T maps to NM_018128.4 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:2227590 G>A maps to NM_018128.4 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr2:3341869 G>T maps to ENST00000398659 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr3:39150701 G>T maps to ENST00000301819 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr2:32983376 C>T maps to NM_017735.4 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr2:33036104 A>T maps to NM_017735.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:38538602 A>C maps to NM_003316.3 R1363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:21644102 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:135277007 G>A maps to NM_007344.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:43570303 G>A maps to NM_015140.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:167755166 A>C maps to NM_031949.4 *593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr17:46847314 G>A maps to NM_001130918.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr2:179597446 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:179639015 G>C maps to NM_133378.4 V2325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr2:179569234 A>G did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr2:179449408 C>A maps to NM_133378.4 A19085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179498762 C>A maps to NM_133378.4 E11587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179542572 C>A maps to NM_133378.4 E10112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179444819 C>T maps to NM_133378.4 R19830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179639176 C>A maps to NM_133378.4 E2272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179565930 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179596284 G>A maps to NM_133378.4 I4492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179464377 A>G maps to NM_133378.4 V16182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179629267 G>T maps to NM_133378.4 S3325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179645958 C>A maps to NM_133378.4 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179568877 G>A maps to NM_133378.4 I8829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179571455 C>T maps to NM_133378.4 A8471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:179592342 G>A maps to NM_133378.4 S5410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:2687614 C>T maps to NM_025250.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:19753676 C>T maps to NM_006001.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:5435794 C>T maps to NM_024803.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:50664758 G>A maps to NM_020461.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:3018700 C>T maps to NM_001160408.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr6:158923253 T>C maps to NM_020245.3 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:15508211 T>G maps to NM_006765.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:139581501 C>A maps to ENST00000358430 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:139563668 G>A maps to ENST00000358430 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:37890276 A>G maps to NM_016616.4 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:7886243 G>A maps to NM_030810.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:672901 C>T maps to NM_001071.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:139972956 C>T maps to NM_207309.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr23:47060922 T>C did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:47074219 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47060345 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr19:34936016 T>C maps to NM_005499.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:34960011 C>A maps to NM_005499.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:68530924 A>G maps to NM_018227.5 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:49847419 G>A maps to NM_003335.2 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr21:43846923 T>C maps to NM_018961.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr17:16285415 G>T maps to NM_018955.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:4200056 G>A maps to NM_003342.4 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr11:57335060 C>A maps to NM_004223.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr23:142967367 G>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:11346071 C>T maps to NM_013319.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:153714146 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:19470545 G>A maps to ENST00000375267 R2703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:93685598 T>A maps to NM_175748.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:26612002 G>A maps to NM_183008.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:62571739 G>A maps to NM_017859.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:234545623 C>A maps to NM_019075.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr2:234628128 C>A maps to NM_007120.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr2:234601883 T>G maps to NM_001072.3 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:234580905 T>G maps to ENST00000373460 L109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:70346620 C>A maps to NM_021139.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr5:35954580 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:100453046 C>A maps to NM_015054.1 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:150267592 G>A maps to NM_025217.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:150386729 G>A maps to NM_024518.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:121151135 C>T maps to NM_001080533.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr9:35381191 C>T maps to ENST00000396787 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:54625987 T>C maps to ENST00000260323 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:176304274 C>T maps to NM_133369.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:24911221 C>T maps to NM_016327.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:118979215 T>A did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr23:118971900 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:229771071 G>T maps to NM_014777.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:45481016 C>T maps to NM_000374.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr1:216595498 G>A maps to ENST00000366943 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:215802206 G>T maps to ENST00000366943 V5180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:215820897 A>C maps to ENST00000366943 A4919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr23:47101056 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:55624552 C>A maps to NM_015306.2 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:55567319 A>G maps to NM_015306.2 G1694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr21:17250146 A>G maps to ENST00000285681 E976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr23:132161819 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:113723355 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr12:109494589 A>C maps to NM_032663.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:11941758 T>G maps to ENST00000399455 Y349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr1:22073589 A>G maps to NM_032236.5 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr23:55515332 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:8989561 A>C maps to NM_003470.2 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41025175 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41043780 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41057953 A>C did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:41055930 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr13:31233270 T>C maps to NM_005800.4 H1019H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:31231669 G>T maps to NM_005800.4 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:129053154 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:7910940 T>G maps to NM_006786.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47517202 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47516991 T>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:82833744 C>T maps to NM_004385.4 G1641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:75830448 G>A maps to NM_014000.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr23:7811257 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:157178087 G>A maps to NM_001167912.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:219296878 G>A maps to NM_007127.2 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr19:53762413 T>A maps to NM_173856.2 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:53770012 T>C maps to NM_173857.2 *302W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:51517793 C>T maps to ENST00000273612 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:100568702 C>T maps to NM_017890.3 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:62201258 G>A maps to NM_020821.2 Y2970Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:62315707 C>A maps to NM_020821.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:2844650 G>T maps to NM_022575.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:465978 G>A maps to NM_001128159.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr23:65242162 A>G did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:98928335 G>A maps to NM_144992.4 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:6101113 G>A maps to NM_000552.3 N2223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:6125980 T>G maps to NM_000552.3 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr10:28822964 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48549532 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48542778 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:48542670 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr13:27257059 C>T maps to NM_006646.5 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr7:70853250 G>A maps to NM_022479.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr14:55429737 G>A maps to NM_007086.3 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr23:48458097 T>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr23:48458031 G>A did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:39230232 T>C maps to NM_025132.3 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr4:39229837 C>T maps to NM_025132.3 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:128471557 C>T maps to NM_018383.4 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:110438052 A>G maps to NM_139281.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr2:29158460 G>A maps to NM_015131.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:117527096 A>C did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr23:48933594 T>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:36574053 A>G maps to NM_001083961.1 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:122361793 C>T maps to NM_144668.4 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr12:122361823 G>T maps to NM_144668.4 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr15:54003561 A>G maps to NM_182758.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr15:53957933 T>C maps to NM_182758.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:64066362 G>A maps to NM_080666.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr14:64066621 A>G maps to NM_080666.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:160112754 C>A maps to NM_001128212.1 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr8:38178628 G>T maps to NM_023034.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1988037 C>T maps to NM_005663.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:38421169 C>T maps to NM_133264.4 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:134232914 C>T maps to NM_003882.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:922929 G>A maps to NM_001184985.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:54277992 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr3:13896247 G>A maps to NM_004625.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:228111949 G>A maps to NM_003395.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr17:44953960 G>A maps to NM_003396.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr17:7606439 C>T maps to NM_018081.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:6023653 C>T maps to NM_015253.1 Y467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:108626508 C>T maps to ENST00000261400 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:160176594 T>G maps to NM_004906.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr23:10066583 C>A did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:6676463 A>G maps to NM_017523.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:123019606 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:168103195 C>A maps to NM_152381.5 S1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:168107531 G>A maps to NM_152381.5 K3210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:168099779 C>T maps to NM_152381.5 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:37586898 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr8:56435861 C>T maps to NM_052898.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr23:100169414 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:128902443 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr22:41320469 A>C maps to NM_022098.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:17228505 G>A maps to NM_022166.3 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr16:17292082 G>A maps to NM_022166.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:17353253 G>A maps to NM_022166.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:19646483 C>A maps to NM_198537.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr14:75265353 C>T maps to NM_019589.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:27411888 C>T maps to NM_139312.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:207222907 G>A maps to NM_018566.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:38272618 A>C maps to NM_024640.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr2:135745258 G>A maps to NM_025052.3 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr2:135745372 G>A maps to NM_025052.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr7:100355877 C>T maps to ENST00000349350 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:100363119 C>T maps to ENST00000349350 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:167016236 C>A maps to ENST00000307529 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:81431736 G>T maps to NM_001105539.1 E864*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-N5-A4RN-01A-12D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:114057896 G>A maps to NM_001164342.1 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:109802551 A>G maps to NM_014797.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:36205546 A>C maps to NM_014383.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:141162801 T>G maps to NM_001080412.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:197128598 G>A maps to NM_194314.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr1:154987607 C>T maps to ENST00000417934 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr18:45556035 C>T maps to NM_001039360.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr23:64719784 T>C did not map to a codon.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr16:88677690 C>T maps to ENST00000452588 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:88666312 C>T maps to ENST00000452588 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr19:47572490 C>A maps to NM_015168.1 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr23:64141739 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:52981591 C>A maps to NM_001009881.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:52991829 G>A maps to NM_001009881.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:87445611 G>A maps to NM_015144.2 H768H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:99998669 G>A maps to NM_017984.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:207173410 G>T maps to NM_020923.1 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:207170662 G>T maps to NM_020923.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:19185897 T>C maps to NM_019028.2 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:44986745 G>A maps to NM_016598.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr12:72030370 T>A maps to NM_144982.4 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr12:72037951 G>A maps to NM_144982.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:72822571 C>T maps to NM_006885.3 Q3201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr8:77766791 G>A maps to NM_024721.4 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr8:77767178 T>C maps to NM_024721.4 H2674H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr15:42742689 C>A maps to NM_022473.1 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr14:69256295 G>C maps to NM_004926.2 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:68598586 C>T maps to NM_133458.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr8:106811073 G>T maps to NM_012082.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:24228959 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr23:24225887 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:79734319 G>T maps to NM_014733.3 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:41099852 C>G maps to NM_001077268.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:68215287 T>C maps to NM_015346.3 S2495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:52704607 G>T maps to NM_004799.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:124266661 T>A maps to NM_007222.3 K509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr13:100634934 C>A maps to NM_007129.2 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr23:136649209 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr13:100617758 C>A maps to NM_033132.3 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr6:28217587 C>A maps to NM_019110.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101139143 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:101139765 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70470016 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70460938 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:70461090 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:35836058 C>T maps to NM_005095.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:50382590 G>A maps to NM_015896.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:288046 C>T maps to NM_006624.4 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr3:44611528 A>T maps to NM_018651.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr3:44612303 C>T maps to NM_018651.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:44684746 C>T maps to NM_006991.3 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:12243601 G>A maps to NM_021143.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:148947338 G>A maps to NM_012256.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:44740348 C>A maps to NM_182490.1 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:44933962 T>C maps to NM_014518.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:44777265 C>A maps to NM_181756.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr11:116649649 C>T maps to NM_003904.3 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr16:31927690 G>T maps to NM_003414.4 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:31925869 G>A maps to NM_003414.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:53303888 C>T maps to NM_006969.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr22:22869288 A>G maps to NM_080740.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr22:22842865 A>G maps to NM_080764.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr19:44352094 C>T maps to NM_181845.1 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:150278112 A>G maps to NM_001172831.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr16:58031929 C>G maps to NM_020807.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr19:58965694 C>T maps to NM_207395.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr19:14817511 T>A maps to NM_032433.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:38344818 C>A maps to NM_006954.1 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr5:178309996 G>T maps to NM_058230.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:7585558 A>G maps to NM_018083.4 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr18:32949294 G>A maps to NM_145756.2 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:44377738 A>G maps to ENST00000324394 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:46724533 C>T maps to NM_024741.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:58438843 A>G maps to NM_133460.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:37581895 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134494611 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134494127 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:57802427 C>T maps to NM_006635.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:37130010 A>C maps to NM_153257.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr9:109765633 G>A maps to NM_021224.4 K2372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:44112549 G>A maps to NM_145312.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:21588647 C>G maps to NM_001076678.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:99521060 C>T maps to NM_014930.1 *684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr10:135125330 G>A maps to NM_145806.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr20:62598841 G>A maps to NM_020713.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr4:10445495 C>T maps to NM_053042.2 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr19:31040263 G>A maps to NM_014717.1 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:31039522 A>G maps to NM_014717.1 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:30934828 C>T maps to NM_014717.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:57839975 C>A maps to NM_213598.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:40514458 G>A maps to NM_178544.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:9583918 T>C maps to NM_152476.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:9577912 T>C maps to NM_152476.2 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr19:37210153 T>C maps to ENST00000423498 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr19:38230643 C>T maps to NM_001172690.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:56935643 G>A maps to NM_001159861.1 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr19:37643368 G>T maps to ENST00000356958 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:52519496 C>A maps to NM_025040.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:52496398 G>A maps to ENST00000354939 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:40574145 G>A maps to NM_001098414.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47919052 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47918898 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:91404617 C>A maps to NM_201269.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:22291305 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:52394224 T>C maps to NM_023074.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:99169913 A>G maps to NM_001083956.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr9:40774077 G>T maps to NM_033160.5 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:56953523 T>C maps to ENST00000342634 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:22375866 T>C maps to NM_001001411.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:22364260 G>T maps to NM_001001411.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr7:63981661 G>A maps to NM_178558.4 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:151261868 C>T maps to NM_020832.1 C829C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:81553672 G>A maps to NM_001033723.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr23:84526454 A>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:21300261 T>G maps to NM_182515.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr4:435657 T>C maps to NM_133474.2 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:57956697 G>T maps to NM_001023561.2 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr17:80788320 C>T maps to NM_024702.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:134427748 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:35273865 A>G maps to NM_014106.3 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr7:150094610 C>T maps to NM_173680.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr7:150094402 G>A maps to NM_173680.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:38027835 G>A maps to NM_001013659.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:12501522 T>C maps to NM_001080821.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr3:113955900 C>T maps to NM_007136.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:53058028 G>A maps to NM_001039886.3 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47775477 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:47775513 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr19:53989941 C>A maps to NM_001004301.3 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:71898076 G>A maps to ENST00000425432 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr19:53116461 A>G maps to NM_018300.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr20:57766697 C>A maps to NM_178457.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:57767906 G>A maps to NM_178457.1 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:52569973 A>T maps to NM_001136499.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr7:50129290 G>A maps to NM_007009.2 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr3:102187874 G>T maps to NM_175056.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr2:135988494 G>A maps to NM_032143.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:58850388 G>A maps to NM_181846.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr17:15884459 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr23:57935106 G>T did not map to a codon.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr23:57619817 G>A did not map to a codon.
Sequencing variant TCGA-ND-A4WC-01A-21D-A28R-08 chr1:53237446 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:143087015 T>C maps to NM_001010972.1 T520T. Only missense variants will be evaluated by CHASM.
