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 | 15 | 72837276 | 72837276 | + | Missense_Mutation | SNP | C | C | G | TCGA-S5-A6DX-01A-11D-A31L-08 | TCGA-S5-A6DX-10A-01D-A31J-08 | g.chr15:72837276C>G | c.559C>G | c.(559-561)Cag>Gag | p.Q187E |
BLCA | 15 | 72837290 | 72837290 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr15:72837290G>C | c.573G>C | c.(571-573)ttG>ttC | p.L191F |
BLCA | 15 | 72875563 | 72875563 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-AA6U-01A-11D-A391-08 | TCGA-DK-AA6U-10A-01D-A394-08 | g.chr15:72875563G>T | c.1604G>T | c.(1603-1605)cGa>cTa | p.R535L |
BRCA | 15 | 72855839 | 72855839 | + | Silent | SNP | T | T | C | TCGA-A8-A07L-01A-11W-A019-09 | TCGA-A8-A07L-10A-01W-A021-09 | g.chr15:72855839T>C | c.909T>C | c.(907-909)ttT>ttC | p.F303F |
BRCA | 15 | 72874491 | 72874491 | + | Missense_Mutation | SNP | C | C | A | TCGA-BH-A2L8-01A-11D-A18P-09 | TCGA-BH-A2L8-10A-01D-A18P-09 | g.chr15:72874491C>A | c.1552C>A | c.(1552-1554)Ctg>Atg | p.L518M |
COAD | 15 | 72855816 | 72855816 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr15:72855816C>T | c.886C>T | c.(886-888)Cgc>Tgc | p.R296C |
COAD | 15 | 72855836 | 72855836 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:72855836A>C | c.906A>C | c.(904-906)caA>caC | p.Q302H |
COAD | 15 | 72873198 | 72873198 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:72873198C>T | c.1342C>T | c.(1342-1344)Cac>Tac | p.H448Y |
COADREAD | 15 | 72847642 | 72847642 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:72847642T>C | c.619T>C | c.(619-621)Ttt>Ctt | p.F207L |
COADREAD | 15 | 72853877 | 72853877 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:72853877A>C | c.791A>C | c.(790-792)aAt>aCt | p.N264T |
COADREAD | 15 | 72855816 | 72855816 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr15:72855816C>T | c.886C>T | c.(886-888)Cgc>Tgc | p.R296C |
COADREAD | 15 | 72855836 | 72855836 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:72855836A>C | c.906A>C | c.(904-906)caA>caC | p.Q302H |
COADREAD | 15 | 72873198 | 72873198 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:72873198C>T | c.1342C>T | c.(1342-1344)Cac>Tac | p.H448Y |
GBM | 15 | 72767077 | 72767077 | + | Missense_Mutation | SNP | G | G | A | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr15:72767077G>A | c.97G>A | c.(97-99)Gac>Aac | p.D33N |
GBMLGG | 15 | 72767077 | 72767077 | + | Missense_Mutation | SNP | G | G | A | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr15:72767077G>A | c.97G>A | c.(97-99)Gac>Aac | p.D33N |
HNSC | 15 | 72873104 | 72873104 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7102-01A-11D-2012-08 | TCGA-CV-7102-10A-01D-2013-08 | g.chr15:72873104C>G | c.1248C>G | c.(1246-1248)ttC>ttG | p.F416L |
KIPAN | 15 | 72847625 | 72847625 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-5470-01A-01D-1501-10 | TCGA-CZ-5470-11A-01D-1501-10 | g.chr15:72847625T>G | c.602T>G | c.(601-603)cTt>cGt | p.L201R |
KIPAN | 15 | 72848195 | 72848195 | + | Silent | SNP | T | T | C | TCGA-B0-5088-01A-01D-1462-08 | TCGA-B0-5088-11A-01D-1462-08 | g.chr15:72848195T>C | c.684T>C | c.(682-684)acT>acC | p.T228T |
KIPAN | 15 | 72855824 | 72855824 | + | Missense_Mutation | SNP | A | A | C | TCGA-2Z-A9JP-01A-11D-A42J-10 | TCGA-2Z-A9JP-10A-01D-A42M-10 | g.chr15:72855824A>C | c.894A>C | c.(892-894)aaA>aaC | p.K298N |
KIPAN | 15 | 72874471 | 72874471 | + | Missense_Mutation | SNP | G | G | C | TCGA-Y8-A894-01A-11D-A35Z-10 | TCGA-Y8-A894-10A-01D-A35Z-10 | g.chr15:72874471G>C | c.1532G>C | c.(1531-1533)cGa>cCa | p.R511P |
KIRC | 15 | 72847625 | 72847625 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-5470-01A-01D-1501-10 | TCGA-CZ-5470-11A-01D-1501-10 | g.chr15:72847625T>G | c.602T>G | c.(601-603)cTt>cGt | p.L201R |
KIRC | 15 | 72848195 | 72848195 | + | Silent | SNP | T | T | C | TCGA-B0-5088-01A-01D-1462-08 | TCGA-B0-5088-11A-01D-1462-08 | g.chr15:72848195T>C | c.684T>C | c.(682-684)acT>acC | p.T228T |
KIRP | 15 | 72855824 | 72855824 | + | Missense_Mutation | SNP | A | A | C | TCGA-2Z-A9JP-01A-11D-A42J-10 | TCGA-2Z-A9JP-10A-01D-A42M-10 | g.chr15:72855824A>C | c.894A>C | c.(892-894)aaA>aaC | p.K298N |
KIRP | 15 | 72874471 | 72874471 | + | Missense_Mutation | SNP | G | G | C | TCGA-Y8-A894-01A-11D-A35Z-10 | TCGA-Y8-A894-10A-01D-A35Z-10 | g.chr15:72874471G>C | c.1532G>C | c.(1531-1533)cGa>cCa | p.R511P |
LIHC | 15 | 72767267 | 72767267 | + | Missense_Mutation | SNP | A | A | G | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr15:72767267A>G | c.287A>G | c.(286-288)gAg>gGg | p.E96G |
LIHC | 15 | 72859489 | 72859489 | + | Missense_Mutation | SNP | A | A | G | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr15:72859489A>G | c.997A>G | c.(997-999)Acc>Gcc | p.T333A |
LUAD | 15 | 72767214 | 72767215 | + | In_Frame_Ins | INS | - | - | GGC | TCGA-55-7816-01A-11D-2167-08 | TCGA-55-7816-10A-01D-2167-08 | g.chr15:72767214_72767215insGGC | c.234_235insGGC | c.(235-237)ggc>GGCggc | p.79_79G>GG |
LUAD | 15 | 72810415 | 72810415 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr15:72810415C>T | c.383C>T | c.(382-384)gCa>gTa | p.A128V |
LUAD | 15 | 72873113 | 72873113 | + | Silent | SNP | T | T | C | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr15:72873113T>C | c.1257T>C | c.(1255-1257)aaT>aaC | p.N419N |
LUAD | 15 | 72873134 | 72873134 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr15:72873134G>T | c.1278G>T | c.(1276-1278)caG>caT | p.Q426H |
LUAD | 15 | 72873191 | 72873191 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr15:72873191G>T | c.1335G>T | c.(1333-1335)atG>atT | p.M445I |
LUAD | 15 | 72873301 | 72873301 | + | Missense_Mutation | SNP | T | T | C | TCGA-99-8032-01A-11D-2238-08 | TCGA-99-8032-10A-01D-2238-08 | g.chr15:72873301T>C | c.1445T>C | c.(1444-1446)cTc>cCc | p.L482P |
OV | 15 | 72847705 | 72847705 | + | Splice_Site | SNP | G | G | A | TCGA-25-1326-01A-01W-0492-08 | TCGA-25-1326-10A-01W-0492-08 | g.chr15:72847705G>A | | c.e4+1 | |
PAAD | 15 | 72853880 | 72853880 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:72853880G>T | c.794G>T | c.(793-795)aGc>aTc | p.S265I |
PAAD | 15 | 72875582 | 72875582 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:72875582G>T | c.1623G>T | c.(1621-1623)caG>caT | p.Q541H |
PRAD | 15 | 72855772 | 72855772 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:72855772G>A | c.842G>A | c.(841-843)tGc>tAc | p.C281Y |
READ | 15 | 72847642 | 72847642 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:72847642T>C | c.619T>C | c.(619-621)Ttt>Ctt | p.F207L |
READ | 15 | 72853877 | 72853877 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:72853877A>C | c.791A>C | c.(790-792)aAt>aCt | p.N264T |
SKCM | 15 | 72837239 | 72837241 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr15:72837239_72837241delGAT | c.522_524delGAT | c.(520-525)cagatg>cag | p.M175del |
SKCM | 15 | 72873292 | 72873292 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr15:72873292C>T | c.1436C>T | c.(1435-1437)gCt>gTt | p.A479V |