Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 21 | 37759967 | 37759967 | + | Silent | SNP | C | C | G | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr21:37759967C>G | c.198C>G | c.(196-198)acC>acG | p.T66T |
BLCA | 21 | 37766929 | 37766929 | + | Silent | SNP | C | C | T | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chr21:37766929C>T | c.462C>T | c.(460-462)atC>atT | p.I154I |
BLCA | 21 | 37775096 | 37775096 | + | Missense_Mutation | SNP | C | C | G | TCGA-KQ-A41S-01A-12D-A339-08 | TCGA-KQ-A41S-10C-01D-A339-08 | g.chr21:37775096C>G | c.704C>G | c.(703-705)tCt>tGt | p.S235C |
BLCA | 21 | 37775105 | 37775105 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr21:37775105G>A | c.713G>A | c.(712-714)cGt>cAt | p.R238H |
BLCA | 21 | 37781087 | 37781087 | + | Silent | SNP | A | A | C | TCGA-FD-A3B7-01A-31D-A20D-08 | TCGA-FD-A3B7-10A-01D-A20D-08 | g.chr21:37781087A>C | c.786A>C | c.(784-786)gtA>gtC | p.V262V |
BLCA | 21 | 37785282 | 37785282 | + | Missense_Mutation | SNP | C | C | A | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr21:37785282C>A | c.1162C>A | c.(1162-1164)Cca>Aca | p.P388T |
BLCA | 21 | 37785421 | 37785421 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr21:37785421C>G | c.1301C>G | c.(1300-1302)cCc>cGc | p.P434R |
BLCA | 21 | 37788621 | 37788621 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr21:37788621G>C | c.1637G>C | c.(1636-1638)aGa>aCa | p.R546T |
BRCA | 21 | 37763873 | 37763873 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr21:37763873T>G | c.284T>G | c.(283-285)gTg>gGg | p.V95G |
BRCA | 21 | 37771831 | 37771831 | + | Silent | SNP | A | A | G | TCGA-E9-A1N4-01A-11D-A14K-09 | TCGA-E9-A1N4-10A-01D-A14K-09 | g.chr21:37771831A>G | c.591A>G | c.(589-591)gtA>gtG | p.V197V |
BRCA | 21 | 37785375 | 37785375 | + | Missense_Mutation | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr21:37785375A>C | c.1255A>C | c.(1255-1257)Acc>Ccc | p.T419P |
COAD | 21 | 37759960 | 37759960 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr21:37759960G>A | c.191G>A | c.(190-192)cGt>cAt | p.R64H |
COAD | 21 | 37781679 | 37781679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:37781679G>A | c.835G>A | c.(835-837)Gct>Act | p.A279T |
COAD | 21 | 37785221 | 37785221 | + | Silent | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr21:37785221C>T | c.1101C>T | c.(1099-1101)gaC>gaT | p.D367D |
COAD | 21 | 37785464 | 37785464 | + | Silent | SNP | C | C | T | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr21:37785464C>T | c.1344C>T | c.(1342-1344)gaC>gaT | p.D448D |
COAD | 21 | 37788591 | 37788591 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr21:37788591A>G | c.1607A>G | c.(1606-1608)cAg>cGg | p.Q536R |
COAD | 21 | 37788614 | 37788614 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr21:37788614C>T | c.1630C>T | c.(1630-1632)Cgg>Tgg | p.R544W |
COADREAD | 21 | 37759960 | 37759960 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr21:37759960G>A | c.191G>A | c.(190-192)cGt>cAt | p.R64H |
COADREAD | 21 | 37766863 | 37766863 | + | Silent | SNP | G | G | A | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr21:37766863G>A | c.396G>A | c.(394-396)gtG>gtA | p.V132V |
COADREAD | 21 | 37781679 | 37781679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:37781679G>A | c.835G>A | c.(835-837)Gct>Act | p.A279T |
COADREAD | 21 | 37785221 | 37785221 | + | Silent | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr21:37785221C>T | c.1101C>T | c.(1099-1101)gaC>gaT | p.D367D |
COADREAD | 21 | 37785464 | 37785464 | + | Silent | SNP | C | C | T | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr21:37785464C>T | c.1344C>T | c.(1342-1344)gaC>gaT | p.D448D |
COADREAD | 21 | 37788591 | 37788591 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr21:37788591A>G | c.1607A>G | c.(1606-1608)cAg>cGg | p.Q536R |
COADREAD | 21 | 37788614 | 37788614 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr21:37788614C>T | c.1630C>T | c.(1630-1632)Cgg>Tgg | p.R544W |
DLBC | 21 | 37787615 | 37787615 | + | Missense_Mutation | SNP | A | A | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr21:37787615A>C | c.1516A>C | c.(1516-1518)Aag>Cag | p.K506Q |
ESCA | 21 | 37771856 | 37771856 | + | Missense_Mutation | SNP | G | G | T | TCGA-R6-A6XQ-01B-11D-A33E-09 | TCGA-R6-A6XQ-10A-01D-A33H-09 | g.chr21:37771856G>T | c.616G>T | c.(616-618)Gct>Tct | p.A206S |
ESCA | 21 | 37775142 | 37775142 | + | Silent | SNP | C | C | T | TCGA-IG-A3Y9-01A-12D-A247-09 | TCGA-IG-A3Y9-10A-01D-A247-09 | g.chr21:37775142C>T | c.750C>T | c.(748-750)ctC>ctT | p.L250L |
ESCA | 21 | 37781696 | 37781696 | + | Silent | SNP | T | T | C | TCGA-XP-A8T8-01A-11D-A36J-09 | TCGA-XP-A8T8-10A-01D-A36M-09 | g.chr21:37781696T>C | c.852T>C | c.(850-852)ccT>ccC | p.P284P |
GBMLGG | 21 | 37775114 | 37775114 | + | Missense_Mutation | SNP | G | G | C | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr21:37775114G>C | c.722G>C | c.(721-723)aGt>aCt | p.S241T |
GBMLGG | 21 | 37785365 | 37785365 | + | Silent | SNP | G | G | A | TCGA-QH-A6CX-01A-11D-A32B-08 | TCGA-QH-A6CX-10A-01D-A329-08 | g.chr21:37785365G>A | c.1245G>A | c.(1243-1245)ccG>ccA | p.P415P |
GBMLGG | 21 | 37787682 | 37787682 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6408-01A-11D-1705-08 | TCGA-DU-6408-10A-01D-1705-08 | g.chr21:37787682A>G | c.1583A>G | c.(1582-1584)cAg>cGg | p.Q528R |
HNSC | 21 | 37769777 | 37769777 | + | Silent | SNP | G | G | A | TCGA-CV-7411-01A-11D-2078-08 | TCGA-CV-7411-10A-01D-2078-08 | g.chr21:37769777G>A | c.546G>A | c.(544-546)ttG>ttA | p.L182L |
HNSC | 21 | 37781744 | 37781744 | + | Silent | SNP | G | G | T | TCGA-IQ-A61G-01A-11D-A30E-08 | TCGA-IQ-A61G-10A-01D-A30H-08 | g.chr21:37781744G>T | c.900G>T | c.(898-900)ctG>ctT | p.L300L |
HNSC | 21 | 37783871 | 37783871 | + | Missense_Mutation | SNP | A | A | T | TCGA-CN-5364-01A-01D-1434-08 | TCGA-CN-5364-10A-01D-1434-08 | g.chr21:37783871A>T | c.1030A>T | c.(1030-1032)Ata>Tta | p.I344L |
HNSC | 21 | 37785298 | 37785298 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-6021-01A-11D-1683-08 | TCGA-CN-6021-10A-01D-1683-08 | g.chr21:37785298G>T | c.1178G>T | c.(1177-1179)aGa>aTa | p.R393I |
HNSC | 21 | 37785504 | 37785504 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr21:37785504G>A | c.1384G>A | c.(1384-1386)Ggg>Agg | p.G462R |
HNSC | 21 | 37788586 | 37788586 | + | Silent | SNP | C | C | T | TCGA-CR-7383-01A-11D-2129-08 | TCGA-CR-7383-10A-01D-2129-08 | g.chr21:37788586C>T | c.1602C>T | c.(1600-1602)gaC>gaT | p.D534D |
HNSC | 21 | 37788639 | 37788639 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-7395-01A-11D-2012-08 | TCGA-CR-7395-10A-01D-2013-08 | g.chr21:37788639G>A | c.1655G>A | c.(1654-1656)gGa>gAa | p.G552E |
KIPAN | 21 | 37783835 | 37783835 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5004-01A-01D-1462-08 | TCGA-BP-5004-11A-01D-1462-08 | g.chr21:37783835A>G | c.994A>G | c.(994-996)Acc>Gcc | p.T332A |
KIPAN | 21 | 37785583 | 37785583 | + | Missense_Mutation | SNP | C | C | G | TCGA-CZ-4859-01A-02D-1429-08 | TCGA-CZ-4859-11A-01D-1429-08 | g.chr21:37785583C>G | c.1463C>G | c.(1462-1464)aCa>aGa | p.T488R |
KIRC | 21 | 37783835 | 37783835 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5004-01A-01D-1462-08 | TCGA-BP-5004-11A-01D-1462-08 | g.chr21:37783835A>G | c.994A>G | c.(994-996)Acc>Gcc | p.T332A |
KIRC | 21 | 37785583 | 37785583 | + | Missense_Mutation | SNP | C | C | G | TCGA-CZ-4859-01A-02D-1429-08 | TCGA-CZ-4859-11A-01D-1429-08 | g.chr21:37785583C>G | c.1463C>G | c.(1462-1464)aCa>aGa | p.T488R |
LGG | 21 | 37775114 | 37775114 | + | Missense_Mutation | SNP | G | G | C | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr21:37775114G>C | c.722G>C | c.(721-723)aGt>aCt | p.S241T |
LGG | 21 | 37785365 | 37785365 | + | Silent | SNP | G | G | A | TCGA-QH-A6CX-01A-11D-A32B-08 | TCGA-QH-A6CX-10A-01D-A329-08 | g.chr21:37785365G>A | c.1245G>A | c.(1243-1245)ccG>ccA | p.P415P |
LGG | 21 | 37787682 | 37787682 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6408-01A-11D-1705-08 | TCGA-DU-6408-10A-01D-1705-08 | g.chr21:37787682A>G | c.1583A>G | c.(1582-1584)cAg>cGg | p.Q528R |
LIHC | 21 | 37785409 | 37785409 | + | Missense_Mutation | SNP | C | C | A | TCGA-CC-A123-01A-11D-A12Z-10 | TCGA-CC-A123-10A-01D-A12Z-10 | g.chr21:37785409C>A | c.1289C>A | c.(1288-1290)cCc>cAc | p.P430H |
LUAD | 21 | 37758467 | 37758467 | + | Silent | SNP | C | C | T | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr21:37758467C>T | c.33C>T | c.(31-33)caC>caT | p.H11H |
LUAD | 21 | 37758546 | 37758546 | + | Missense_Mutation | SNP | G | G | A | TCGA-J2-8194-01A-11D-2238-08 | TCGA-J2-8194-10A-01D-2238-08 | g.chr21:37758546G>A | c.112G>A | c.(112-114)Gac>Aac | p.D38N |
LUAD | 21 | 37775077 | 37775077 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7150-01A-21D-2036-08 | TCGA-78-7150-10A-01D-2036-08 | g.chr21:37775077C>T | c.685C>T | c.(685-687)Cac>Tac | p.H229Y |
LUAD | 21 | 37775118 | 37775118 | + | Silent | SNP | C | C | T | TCGA-38-4625-01A-01D-1553-08 | TCGA-38-4625-11A-01D-1553-08 | g.chr21:37775118C>T | c.726C>T | c.(724-726)ttC>ttT | p.F242F |
LUAD | 21 | 37785246 | 37785246 | + | Missense_Mutation | SNP | G | G | C | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr21:37785246G>C | c.1126G>C | c.(1126-1128)Gag>Cag | p.E376Q |
LUAD | 21 | 37785450 | 37785450 | + | Missense_Mutation | SNP | A | A | G | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr21:37785450A>G | c.1330A>G | c.(1330-1332)Aca>Gca | p.T444A |
LUSC | 21 | 37763859 | 37763859 | + | Silent | SNP | C | C | A | TCGA-37-4141-01A-02D-1352-08 | TCGA-37-4141-10A-01D-1352-08 | g.chr21:37763859C>A | c.270C>A | c.(268-270)atC>atA | p.I90I |
LUSC | 21 | 37775112 | 37775112 | + | Silent | SNP | G | G | T | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr21:37775112G>T | c.720G>T | c.(718-720)ctG>ctT | p.L240L |
LUSC | 21 | 37788602 | 37788602 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr21:37788602C>T | c.1618C>T | c.(1618-1620)Cca>Tca | p.P540S |
OV | 21 | 37758546 | 37758546 | + | Missense_Mutation | SNP | G | G | T | TCGA-13-0760-01A-01W-0372-09 | TCGA-13-0760-10A-01W-0372-09 | g.chr21:37758546G>T | c.112G>T | c.(112-114)Gac>Tac | p.D38Y |
PAAD | 21 | 37763902 | 37763902 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:37763902G>A | c.313G>A | c.(313-315)Gct>Act | p.A105T |
PAAD | 21 | 37769717 | 37769717 | + | Silent | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:37769717A>G | c.486A>G | c.(484-486)caA>caG | p.Q162Q |
PAAD | 21 | 37781761 | 37781761 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:37781761C>T | c.917C>T | c.(916-918)aCa>aTa | p.T306I |
PAAD | 21 | 37783861 | 37783861 | + | Silent | SNP | C | C | T | TCGA-2J-AAB1-01A-11D-A40W-08 | TCGA-2J-AAB1-10A-01D-A40W-08 | g.chr21:37783861C>T | c.1020C>T | c.(1018-1020)taC>taT | p.Y340Y |
PRAD | 21 | 37781094 | 37781094 | + | Missense_Mutation | SNP | A | A | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr21:37781094A>G | c.793A>G | c.(793-795)Acc>Gcc | p.T265A |
READ | 21 | 37766863 | 37766863 | + | Silent | SNP | G | G | A | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr21:37766863G>A | c.396G>A | c.(394-396)gtG>gtA | p.V132V |
SKCM | 21 | 37766889 | 37766889 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr21:37766889G>A | c.422G>A | c.(421-423)gGg>gAg | p.G141E |
SKCM | 21 | 37785199 | 37785199 | + | Missense_Mutation | SNP | T | T | G | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr21:37785199T>G | c.1079T>G | c.(1078-1080)tTc>tGc | p.F360C |
SKCM | 21 | 37785272 | 37785272 | + | Silent | SNP | G | G | A | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chr21:37785272G>A | c.1152G>A | c.(1150-1152)ttG>ttA | p.L384L |
SKCM | 21 | 37785495 | 37785495 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C8-06A-12D-A30X-08 | TCGA-GF-A6C8-10A-01D-A30X-08 | g.chr21:37785495C>T | c.1375C>T | c.(1375-1377)Ccc>Tcc | p.P459S |
SKCM | 21 | 37785496 | 37785496 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr21:37785496C>T | c.1376C>T | c.(1375-1377)cCc>cTc | p.P459L |
SKCM | 21 | 37788600 | 37788600 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr21:37788600C>T | c.1616C>T | c.(1615-1617)cCc>cTc | p.P539L |
BLCA | 10 | 28345491 | 28345491 | + | Missense_Mutation | SNP | G | G | A | TCGA-K4-A83P-01A-11D-A34U-08 | TCGA-K4-A83P-10A-01D-A34X-08 | g.chr10:28345491G>A | c.1469C>T | c.(1468-1470)tCa>tTa | p.S490L |
BLCA | 10 | 28348590 | 28348590 | + | Silent | SNP | T | T | C | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr10:28348590T>C | c.1287A>G | c.(1285-1287)gtA>gtG | p.V429V |
BLCA | 10 | 28358781 | 28358781 | + | Splice_Site | SNP | C | C | A | TCGA-E7-A3Y1-01A-11D-A22Z-08 | TCGA-E7-A3Y1-10A-01D-A22Z-08 | g.chr10:28358781C>A | c.1124G>T | c.(1123-1125)gGt>gTt | p.G375V |
BLCA | 10 | 28358782 | 28358782 | + | Splice_Site | SNP | C | C | A | TCGA-E7-A3Y1-01A-11D-A22Z-08 | TCGA-E7-A3Y1-10A-01D-A22Z-08 | g.chr10:28358782C>A | | c.e13-1 | |
BLCA | 10 | 28378735 | 28378735 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chr10:28378735C>G | c.988G>C | c.(988-990)Gat>Cat | p.D330H |
BLCA | 10 | 28409311 | 28409311 | + | Missense_Mutation | SNP | G | G | C | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr10:28409311G>C | c.699C>G | c.(697-699)atC>atG | p.I233M |
BLCA | 10 | 28420612 | 28420612 | + | Silent | SNP | G | G | A | TCGA-XF-AAML-01A-11D-A42E-08 | TCGA-XF-AAML-10A-01D-A42H-08 | g.chr10:28420612G>A | c.324C>T | c.(322-324)ctC>ctT | p.L108L |
BLCA | 10 | 28491177 | 28491177 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr10:28491177G>C | c.61C>G | c.(61-63)Ctg>Gtg | p.L21V |
BLCA | 10 | 28527520 | 28527520 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chr10:28527520G>A | c.14C>T | c.(13-15)tCa>tTa | p.S5L |
BRCA | 10 | 28378743 | 28378743 | + | Missense_Mutation | SNP | C | C | G | TCGA-EW-A1P4-01A-21D-A142-09 | TCGA-EW-A1P4-10A-01D-A142-09 | g.chr10:28378743C>G | c.980G>C | c.(979-981)aGt>aCt | p.S327T |
BRCA | 10 | 28409186 | 28409186 | + | Missense_Mutation | SNP | G | G | C | TCGA-B6-A400-01A-11D-A23C-09 | TCGA-B6-A400-10A-01D-A23C-09 | g.chr10:28409186G>C | c.824C>G | c.(823-825)gCg>gGg | p.A275G |
BRCA | 10 | 28412995 | 28412995 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AC-A62Y-01A-11D-A29N-09 | TCGA-AC-A62Y-10A-01D-A29N-09 | g.chr10:28412995C>A | c.580G>T | c.(580-582)Gag>Tag | p.E194* |
BRCA | 10 | 28436429 | 28436429 | + | Missense_Mutation | SNP | A | A | G | TCGA-B6-A0I5-01A-11W-A100-09 | TCGA-B6-A0I5-10A-01W-A055-09 | g.chr10:28436429A>G | c.298T>C | c.(298-300)Tca>Cca | p.S100P |
CESC | 10 | 28358735 | 28358735 | + | Silent | SNP | G | G | A | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr10:28358735G>A | c.1170C>T | c.(1168-1170)atC>atT | p.I390I |
CESC | 10 | 28408627 | 28408627 | + | Missense_Mutation | SNP | C | C | T | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr10:28408627C>T | c.905G>A | c.(904-906)cGa>cAa | p.R302Q |
CESC | 10 | 28420622 | 28420622 | + | Splice_Site | SNP | T | T | C | TCGA-C5-A7CJ-01A-11D-A32I-09 | TCGA-C5-A7CJ-10A-01D-A32I-09 | g.chr10:28420622T>C | | c.e6-2 | |
CHOL | 10 | 28413008 | 28413008 | + | Silent | SNP | G | G | A | TCGA-W5-AA38-01A-11D-A417-09 | TCGA-W5-AA38-10A-01D-A41A-09 | g.chr10:28413008G>A | c.567C>T | c.(565-567)aaC>aaT | p.N189N |
COAD | 10 | 28343103 | 28343103 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr10:28343103T>C | c.1622A>G | c.(1621-1623)aAa>aGa | p.K541R |
COAD | 10 | 28347489 | 28347489 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr10:28347489T>A | c.1342A>T | c.(1342-1344)Agt>Tgt | p.S448C |
COAD | 10 | 28408644 | 28408644 | + | Splice_Site | SNP | C | C | T | TCGA-DM-A28F-01A-11D-A16V-10 | TCGA-DM-A28F-10A-01D-A16V-10 | g.chr10:28408644C>T | c.888G>A | c.(886-888)agG>agA | p.R296R |
COAD | 10 | 28408646 | 28408646 | + | Splice_Site | SNP | T | T | C | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr10:28408646T>C | | c.e11-2 | |
COAD | 10 | 28408646 | 28408646 | + | Splice_Site | SNP | T | T | C | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr10:28408646T>C | | c.e11-2 | |
COADREAD | 10 | 28343023 | 28343023 | + | Missense_Mutation | SNP | A | A | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr10:28343023A>T | c.1702T>A | c.(1702-1704)Tgg>Agg | p.W568R |
COADREAD | 10 | 28343103 | 28343103 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr10:28343103T>C | c.1622A>G | c.(1621-1623)aAa>aGa | p.K541R |
COADREAD | 10 | 28347489 | 28347489 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr10:28347489T>A | c.1342A>T | c.(1342-1344)Agt>Tgt | p.S448C |
COADREAD | 10 | 28348654 | 28348654 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:28348654C>A | c.1223G>T | c.(1222-1224)aGa>aTa | p.R408I |
COADREAD | 10 | 28408644 | 28408644 | + | Splice_Site | SNP | C | C | T | TCGA-DM-A28F-01A-11D-A16V-10 | TCGA-DM-A28F-10A-01D-A16V-10 | g.chr10:28408644C>T | c.888G>A | c.(886-888)agG>agA | p.R296R |
COADREAD | 10 | 28408646 | 28408646 | + | Splice_Site | SNP | T | T | C | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr10:28408646T>C | | c.e11-2 | |
COADREAD | 10 | 28408646 | 28408646 | + | Splice_Site | SNP | T | T | C | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr10:28408646T>C | | c.e11-2 | |
COADREAD | 10 | 28420579 | 28420579 | + | Silent | SNP | G | G | A | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr10:28420579G>A | c.357C>T | c.(355-357)taC>taT | p.Y119Y |
COADREAD | 10 | 28527516 | 28527516 | + | Silent | SNP | C | C | T | TCGA-AG-3608-01A-01W-0833-10 | TCGA-AG-3608-10A-01W-0833-10 | g.chr10:28527516C>T | c.18G>A | c.(16-18)acG>acA | p.T6T |
DLBC | 10 | 28412969 | 28412969 | + | Missense_Mutation | SNP | T | T | C | TCGA-FF-8042-01A-11D-2210-10 | TCGA-FF-8042-10A-01D-2210-10 | g.chr10:28412969T>C | c.606A>G | c.(604-606)atA>atG | p.I202M |
DLBC | 10 | 28420542 | 28420542 | + | Missense_Mutation | SNP | C | C | T | TCGA-FF-A7CW-01A-11D-A382-10 | TCGA-FF-A7CW-10A-01D-A385-10 | g.chr10:28420542C>T | c.394G>A | c.(394-396)Gat>Aat | p.D132N |
DLBC | 10 | 28527517 | 28527517 | + | Missense_Mutation | SNP | G | G | A | TCGA-FF-8047-01A-11D-2210-10 | TCGA-FF-8047-10A-01D-2210-10 | g.chr10:28527517G>A | c.17C>T | c.(16-18)aCg>aTg | p.T6M |
ESCA | 10 | 28348649 | 28348649 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A6QS-01A-12D-A33E-09 | TCGA-IG-A6QS-10B-01D-A33H-09 | g.chr10:28348649G>T | c.1228C>A | c.(1228-1230)Cag>Aag | p.Q410K |
ESCA | 10 | 28378763 | 28378763 | + | Silent | SNP | A | A | G | TCGA-2H-A9GH-01A-11D-A37C-09 | TCGA-2H-A9GH-11A-11D-A37F-09 | g.chr10:28378763A>G | c.960T>C | c.(958-960)ttT>ttC | p.F320F |
GBM | 10 | 28345469 | 28345469 | + | Silent | SNP | T | T | C | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr10:28345469T>C | c.1491A>G | c.(1489-1491)acA>acG | p.T497T |
GBM | 10 | 28378639 | 28378639 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-27-2521-01A-01D-1494-08 | TCGA-27-2521-10A-01D-1494-08 | g.chr10:28378639G>A | c.1084C>T | c.(1084-1086)Cga>Tga | p.R362* |
GBM | 10 | 28409253 | 28409254 | + | Missense_Mutation | DNP | CA | CA | AG | TCGA-02-2483-01A-01D-1494-08 | TCGA-02-2483-10A-01D-1494-08 | g.chr10:28409253_28409254CA>AG | c.756_757TG>CT | c.(754-759)gcTGgg>gcCTgg | p.G253W |
GBM | 10 | 28420514 | 28420514 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0213-01A-01D-1491-08 | TCGA-06-0213-10A-01D-1491-08 | g.chr10:28420514C>T | c.422G>A | c.(421-423)cGt>cAt | p.R141H |
GBMLGG | 10 | 28345469 | 28345469 | + | Silent | SNP | T | T | C | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr10:28345469T>C | c.1491A>G | c.(1489-1491)acA>acG | p.T497T |
GBMLGG | 10 | 28345529 | 28345529 | + | Silent | SNP | T | T | C | TCGA-HW-8319-01A-11D-2395-08 | TCGA-HW-8319-10A-01D-2396-08 | g.chr10:28345529T>C | c.1431A>G | c.(1429-1431)ctA>ctG | p.L477L |
GBMLGG | 10 | 28348654 | 28348654 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28348654C>A | c.1223G>T | c.(1222-1224)aGa>aTa | p.R408I |
GBMLGG | 10 | 28358723 | 28358723 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28358723C>T | c.1182G>A | c.(1180-1182)caG>caA | p.Q394Q |
GBMLGG | 10 | 28378639 | 28378639 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-27-2521-01A-01D-1494-08 | TCGA-27-2521-10A-01D-1494-08 | g.chr10:28378639G>A | c.1084C>T | c.(1084-1086)Cga>Tga | p.R362* |
GBMLGG | 10 | 28378749 | 28378749 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A5TP-01A-11D-A289-08 | TCGA-DU-A5TP-10A-01D-A289-08 | g.chr10:28378749C>T | c.974G>A | c.(973-975)cGt>cAt | p.R325H |
GBMLGG | 10 | 28378749 | 28378749 | + | Missense_Mutation | SNP | C | C | T | TCGA-S9-A6UA-01A-12D-A33T-08 | TCGA-S9-A6UA-10A-01D-A33W-08 | g.chr10:28378749C>T | c.974G>A | c.(973-975)cGt>cAt | p.R325H |
GBMLGG | 10 | 28409253 | 28409254 | + | Missense_Mutation | DNP | CA | CA | AG | TCGA-02-2483-01A-01D-1494-08 | TCGA-02-2483-10A-01D-1494-08 | g.chr10:28409253_28409254CA>AG | c.756_757TG>CT | c.(754-759)gcTGgg>gcCTgg | p.G253W |
GBMLGG | 10 | 28414006 | 28414006 | + | Silent | SNP | C | C | T | TCGA-HT-8563-01A-11D-2395-08 | TCGA-HT-8563-10A-01D-2396-08 | g.chr10:28414006C>T | c.462G>A | c.(460-462)aaG>aaA | p.K154K |
GBMLGG | 10 | 28420514 | 28420514 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0213-01A-01D-1491-08 | TCGA-06-0213-10A-01D-1491-08 | g.chr10:28420514C>T | c.422G>A | c.(421-423)cGt>cAt | p.R141H |
HNSC | 10 | 28378644 | 28378644 | + | Missense_Mutation | SNP | T | T | C | TCGA-BA-A6DG-01A-21D-A30E-08 | TCGA-BA-A6DG-10A-01D-A30H-08 | g.chr10:28378644T>C | c.1079A>G | c.(1078-1080)tAt>tGt | p.Y360C |
HNSC | 10 | 28409159 | 28409159 | + | Missense_Mutation | SNP | C | C | A | TCGA-F7-A61S-01A-11D-A28R-08 | TCGA-F7-A61S-10A-01D-A28U-08 | g.chr10:28409159C>A | c.851G>T | c.(850-852)aGg>aTg | p.R284M |
HNSC | 10 | 28409531 | 28409531 | + | Missense_Mutation | SNP | C | C | G | TCGA-CN-A49B-01A-31D-A24D-08 | TCGA-CN-A49B-10A-01D-A24F-08 | g.chr10:28409531C>G | c.682G>C | c.(682-684)Gaa>Caa | p.E228Q |
HNSC | 10 | 28413008 | 28413008 | + | Silent | SNP | G | G | A | TCGA-CV-6436-01A-11D-1683-08 | TCGA-CV-6436-11A-01D-1683-08 | g.chr10:28413008G>A | c.567C>T | c.(565-567)aaC>aaT | p.N189N |
HNSC | 10 | 28413037 | 28413037 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A6V7-01A-12D-A34J-08 | TCGA-CN-A6V7-10A-01D-A34M-08 | g.chr10:28413037G>A | c.538C>T | c.(538-540)Cat>Tat | p.H180Y |
LGG | 10 | 28345529 | 28345529 | + | Silent | SNP | T | T | C | TCGA-HW-8319-01A-11D-2395-08 | TCGA-HW-8319-10A-01D-2396-08 | g.chr10:28345529T>C | c.1431A>G | c.(1429-1431)ctA>ctG | p.L477L |
LGG | 10 | 28348654 | 28348654 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28348654C>A | c.1223G>T | c.(1222-1224)aGa>aTa | p.R408I |
LGG | 10 | 28358723 | 28358723 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28358723C>T | c.1182G>A | c.(1180-1182)caG>caA | p.Q394Q |
LGG | 10 | 28378749 | 28378749 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A5TP-01A-11D-A289-08 | TCGA-DU-A5TP-10A-01D-A289-08 | g.chr10:28378749C>T | c.974G>A | c.(973-975)cGt>cAt | p.R325H |
LGG | 10 | 28378749 | 28378749 | + | Missense_Mutation | SNP | C | C | T | TCGA-S9-A6UA-01A-12D-A33T-08 | TCGA-S9-A6UA-10A-01D-A33W-08 | g.chr10:28378749C>T | c.974G>A | c.(973-975)cGt>cAt | p.R325H |
LGG | 10 | 28414006 | 28414006 | + | Silent | SNP | C | C | T | TCGA-HT-8563-01A-11D-2395-08 | TCGA-HT-8563-10A-01D-2396-08 | g.chr10:28414006C>T | c.462G>A | c.(460-462)aaG>aaA | p.K154K |
LIHC | 10 | 28378706 | 28378706 | + | Silent | SNP | T | T | C | TCGA-DD-A4NV-01A-11D-A30V-10 | TCGA-DD-A4NV-10A-01D-A30V-10 | g.chr10:28378706T>C | c.1017A>G | c.(1015-1017)gaA>gaG | p.E339E |
LIHC | 10 | 28420525 | 28420525 | + | Silent | SNP | T | T | C | TCGA-BC-A10T-01A-11D-A12Z-10 | TCGA-BC-A10T-11A-11D-A12Z-10 | g.chr10:28420525T>C | c.411A>G | c.(409-411)gtA>gtG | p.V137V |
LIHC | 10 | 28491163 | 28491163 | + | Silent | SNP | C | C | A | TCGA-DD-AACK-01A-11D-A40R-10 | TCGA-DD-AACK-10A-01D-A40U-10 | g.chr10:28491163C>A | c.75G>T | c.(73-75)ctG>ctT | p.L25L |
LUAD | 10 | 28348647 | 28348647 | + | Silent | SNP | C | C | T | TCGA-MN-A4N5-01A-11D-A24P-08 | TCGA-MN-A4N5-10A-01D-A24P-08 | g.chr10:28348647C>T | c.1230G>A | c.(1228-1230)caG>caA | p.Q410Q |
LUAD | 10 | 28378646 | 28378646 | + | Silent | SNP | C | C | A | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr10:28378646C>A | c.1077G>T | c.(1075-1077)ccG>ccT | p.P359P |
LUSC | 10 | 28345494 | 28345494 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr10:28345494G>T | c.1466C>A | c.(1465-1467)cCa>cAa | p.P489Q |
LUSC | 10 | 28345547 | 28345547 | + | Silent | SNP | C | C | T | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr10:28345547C>T | c.1413G>A | c.(1411-1413)gtG>gtA | p.V471V |
LUSC | 10 | 28348580 | 28348580 | + | Splice_Site | SNP | T | T | C | TCGA-22-5480-01A-01D-1632-08 | TCGA-22-5480-11A-01D-1632-08 | g.chr10:28348580T>C | c.1297A>G | c.(1297-1299)Aag>Gag | p.K433E |
LUSC | 10 | 28348635 | 28348635 | + | Silent | SNP | A | A | T | TCGA-51-4080-01A-01D-1458-08 | TCGA-51-4080-11A-01D-1458-08 | g.chr10:28348635A>T | c.1242T>A | c.(1240-1242)ggT>ggA | p.G414G |
LUSC | 10 | 28348669 | 28348669 | + | Missense_Mutation | SNP | G | G | A | TCGA-39-5035-01A-01D-1441-08 | TCGA-39-5035-11A-01D-1441-08 | g.chr10:28348669G>A | c.1208C>T | c.(1207-1209)aCc>aTc | p.T403I |
LUSC | 10 | 28420572 | 28420572 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2759-01A-01D-1522-08 | TCGA-66-2759-11A-01D-1522-08 | g.chr10:28420572C>A | c.364G>T | c.(364-366)Gtg>Ttg | p.V122L |
OV | 10 | 28378746 | 28378746 | + | Missense_Mutation | SNP | A | A | C | TCGA-04-1644-01B-01D-1526-09 | TCGA-04-1644-11A-01D-1526-09 | g.chr10:28378746A>C | c.977T>G | c.(976-978)cTt>cGt | p.L326R |
OV | 10 | 28408644 | 28408644 | + | Splice_Site | SNP | C | C | G | TCGA-13-1412-01A-01W-0494-09 | TCGA-13-1412-10A-01W-0495-09 | g.chr10:28408644C>G | c.888G>C | c.(886-888)agG>agC | p.R296S |
PAAD | 10 | 28345483 | 28345483 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:28345483G>A | c.1477C>T | c.(1477-1479)Cgt>Tgt | p.R493C |
PAAD | 10 | 28412986 | 28412986 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-IB-A7LX-01A-12D-A36O-08 | TCGA-IB-A7LX-10A-01D-A367-08 | g.chr10:28412986delT | c.589delA | c.(589-591)aggfs | p.R197fs |
PRAD | 10 | 28358764 | 28358764 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:28358764G>A | c.1141C>T | c.(1141-1143)Ctg>Ttg | p.L381L |
READ | 10 | 28343023 | 28343023 | + | Missense_Mutation | SNP | A | A | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr10:28343023A>T | c.1702T>A | c.(1702-1704)Tgg>Agg | p.W568R |
READ | 10 | 28348654 | 28348654 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:28348654C>A | c.1223G>T | c.(1222-1224)aGa>aTa | p.R408I |
READ | 10 | 28420579 | 28420579 | + | Silent | SNP | G | G | A | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr10:28420579G>A | c.357C>T | c.(355-357)taC>taT | p.Y119Y |
READ | 10 | 28527516 | 28527516 | + | Silent | SNP | C | C | T | TCGA-AG-3608-01A-01W-0833-10 | TCGA-AG-3608-10A-01W-0833-10 | g.chr10:28527516C>T | c.18G>A | c.(16-18)acG>acA | p.T6T |
SKCM | 10 | 28343065 | 28343065 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28343065C>T | c.1660G>A | c.(1660-1662)Gag>Aag | p.E554K |
SKCM | 10 | 28343131 | 28343131 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr10:28343131C>T | c.1594G>A | c.(1594-1596)Gaa>Aaa | p.E532K |
SKCM | 10 | 28345429 | 28345429 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr10:28345429C>T | c.1531G>A | c.(1531-1533)Ggt>Agt | p.G511S |
SKCM | 10 | 28347511 | 28347511 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-EE-A29A-06A-12D-A196-08 | TCGA-EE-A29A-10A-01D-A198-08 | g.chr10:28347511A>T | c.1320T>A | c.(1318-1320)taT>taA | p.Y440* |
SKCM | 10 | 28347518 | 28347518 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29C-06A-21D-A197-08 | TCGA-EE-A29C-10A-01D-A199-08 | g.chr10:28347518C>T | c.1313G>A | c.(1312-1314)gGa>gAa | p.G438E |
SKCM | 10 | 28347533 | 28347533 | + | Splice_Site | SNP | C | C | T | TCGA-D3-A2J8-06A-11D-A196-08 | TCGA-D3-A2J8-10A-01D-A198-08 | g.chr10:28347533C>T | | c.e15-1 | |
SKCM | 10 | 28348640 | 28348640 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr10:28348640C>T | c.1237G>A | c.(1237-1239)Gat>Aat | p.D413N |
SKCM | 10 | 28348673 | 28348673 | + | Splice_Site | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28348673C>T | | c.e14-1 | |
SKCM | 10 | 28358748 | 28358748 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:28358748C>T | c.1157G>A | c.(1156-1158)cGa>cAa | p.R386Q |
SKCM | 10 | 28358748 | 28358748 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr10:28358748C>T | c.1157G>A | c.(1156-1158)cGa>cAa | p.R386Q |
SKCM | 10 | 28358748 | 28358748 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr10:28358748C>T | c.1157G>A | c.(1156-1158)cGa>cAa | p.R386Q |
SKCM | 10 | 28358748 | 28358748 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A2NC-06A-11D-A197-08 | TCGA-ER-A2NC-10A-01D-A199-08 | g.chr10:28358748C>T | c.1157G>A | c.(1156-1158)cGa>cAa | p.R386Q |
SKCM | 10 | 28378638 | 28378638 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28378638C>T | c.1085G>A | c.(1084-1086)cGa>cAa | p.R362Q |
SKCM | 10 | 28378648 | 28378648 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28378648G>A | c.1075C>T | c.(1075-1077)Ccg>Tcg | p.P359S |
SKCM | 10 | 28378660 | 28378660 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:28378660C>T | c.1063G>A | c.(1063-1065)Gaa>Aaa | p.E355K |
SKCM | 10 | 28378660 | 28378660 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr10:28378660C>T | c.1063G>A | c.(1063-1065)Gaa>Aaa | p.E355K |
SKCM | 10 | 28378684 | 28378684 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I1-06A-12D-A196-08 | TCGA-DA-A1I1-10A-01D-A198-08 | g.chr10:28378684C>T | c.1039G>A | c.(1039-1041)Gac>Aac | p.D347N |
SKCM | 10 | 28378716 | 28378716 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr10:28378716G>A | c.1007C>T | c.(1006-1008)tCc>tTc | p.S336F |
SKCM | 10 | 28378745 | 28378745 | + | Silent | SNP | A | A | G | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr10:28378745A>G | c.978T>C | c.(976-978)ctT>ctC | p.L326L |
SKCM | 10 | 28378750 | 28378750 | + | Missense_Mutation | SNP | G | G | A | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:28378750G>A | c.973C>T | c.(973-975)Cgt>Tgt | p.R325C |
SKCM | 10 | 28408587 | 28408587 | + | Silent | SNP | C | C | T | TCGA-D3-A2J7-06A-11D-A196-08 | TCGA-D3-A2J7-10A-01D-A198-08 | g.chr10:28408587C>T | c.945G>A | c.(943-945)agG>agA | p.R315R |
SKCM | 10 | 28409123 | 28409123 | + | Splice_Site | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28409123C>T | c.887G>A | c.(886-888)aGg>aAg | p.R296K |
SKCM | 10 | 28409131 | 28409131 | + | Silent | SNP | G | G | A | TCGA-ER-A199-06A-11D-A197-08 | TCGA-ER-A199-10A-01D-A199-08 | g.chr10:28409131G>A | c.879C>T | c.(877-879)ttC>ttT | p.F293F |
SKCM | 10 | 28409178 | 28409178 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr10:28409178C>T | c.832G>A | c.(832-834)Gaa>Aaa | p.E278K |
SKCM | 10 | 28409221 | 28409221 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr10:28409221C>T | c.789G>A | c.(787-789)caG>caA | p.Q263Q |
SKCM | 10 | 28409223 | 28409223 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-ER-A19J-06A-11D-A196-08 | TCGA-ER-A19J-10A-01D-A198-08 | g.chr10:28409223G>A | c.787C>T | c.(787-789)Cag>Tag | p.Q263* |
SKCM | 10 | 28409238 | 28409238 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr10:28409238T>G | c.772A>C | c.(772-774)Aag>Cag | p.K258Q |
SKCM | 10 | 28409259 | 28409259 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr10:28409259C>T | c.751G>A | c.(751-753)Gaa>Aaa | p.E251K |
SKCM | 10 | 28409259 | 28409259 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr10:28409259C>T | c.751G>A | c.(751-753)Gaa>Aaa | p.E251K |
SKCM | 10 | 28409261 | 28409261 | + | Missense_Mutation | SNP | T | T | C | TCGA-GN-A4U3-06A-11D-A32N-08 | TCGA-GN-A4U3-10F-01D-A32N-08 | g.chr10:28409261T>C | c.749A>G | c.(748-750)aAg>aGg | p.K250R |
SKCM | 10 | 28409262 | 28409262 | + | Missense_Mutation | SNP | T | T | C | TCGA-GN-A4U3-06A-11D-A32N-08 | TCGA-GN-A4U3-10F-01D-A32N-08 | g.chr10:28409262T>C | c.748A>G | c.(748-750)Aag>Gag | p.K250E |
SKCM | 10 | 28409304 | 28409304 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr10:28409304G>A | c.706C>T | c.(706-708)Ctc>Ttc | p.L236F |
SKCM | 10 | 28409531 | 28409531 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28409531C>T | c.682G>A | c.(682-684)Gaa>Aaa | p.E228K |
SKCM | 10 | 28412977 | 28412977 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4F9-06A-11D-A24R-08 | TCGA-FS-A4F9-10A-01D-A24R-08 | g.chr10:28412977C>T | c.598G>A | c.(598-600)Gaa>Aaa | p.E200K |
SKCM | 10 | 28413985 | 28413985 | + | Silent | SNP | C | C | T | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr10:28413985C>T | c.483G>A | c.(481-483)gcG>gcA | p.A161A |
SKCM | 10 | 28414002 | 28414002 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZB-06A-12D-A197-08 | TCGA-FS-A1ZB-10A-01D-A199-08 | g.chr10:28414002C>T | c.466G>A | c.(466-468)Gat>Aat | p.D156N |
SKCM | 10 | 28420502 | 28420502 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:28420502T>A | c.434A>T | c.(433-435)aAt>aTt | p.N145I |
SKCM | 10 | 28420515 | 28420515 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A268-06A-11D-A196-08 | TCGA-GN-A268-10A-01D-A198-08 | g.chr10:28420515G>A | c.421C>T | c.(421-423)Cgt>Tgt | p.R141C |
SKCM | 10 | 28420537 | 28420537 | + | Silent | SNP | C | C | T | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr10:28420537C>T | c.399G>A | c.(397-399)gaG>gaA | p.E133E |
SKCM | 10 | 28420539 | 28420539 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr10:28420539C>T | c.397G>A | c.(397-399)Gag>Aag | p.E133K |
SKCM | 10 | 28420551 | 28420551 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr10:28420551C>T | c.385G>A | c.(385-387)Gat>Aat | p.D129N |
SKCM | 10 | 28420556 | 28420556 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:28420556G>A | c.380C>T | c.(379-381)cCt>cTt | p.P127L |
SKCM | 10 | 28420578 | 28420578 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1QA-06A-11D-A196-08 | TCGA-D3-A1QA-10A-01D-A198-08 | g.chr10:28420578C>T | c.358G>A | c.(358-360)Gac>Aac | p.D120N |
SKCM | 10 | 28420578 | 28420578 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr10:28420578C>T | c.358G>A | c.(358-360)Gac>Aac | p.D120N |
SKCM | 10 | 28420578 | 28420578 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A149-06A-11D-A196-08 | TCGA-D9-A149-10A-01D-A198-08 | g.chr10:28420578C>T | c.358G>A | c.(358-360)Gac>Aac | p.D120N |
SKCM | 10 | 28491141 | 28491141 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:28491141C>T | c.97G>A | c.(97-99)Gaa>Aaa | p.E33K |