| 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 |
|---|
| ACC | 3 | 73432786 | 73432788 | + | In_Frame_Del | DEL | CTC | CTC | - | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr3:73432786_73432788delCTC | c.2929_2931delGAG | c.(2929-2931)gagdel | p.E977del |
| ACC | 3 | 73437153 | 73437153 | + | Missense_Mutation | SNP | T | T | C | TCGA-OR-A5K9-01A-11D-A29I-10 | TCGA-OR-A5K9-11A-11D-A29L-10 | g.chr3:73437153T>C | c.1484A>G | c.(1483-1485)aAc>aGc | p.N495S |
| BLCA | 3 | 73432631 | 73432631 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-A9RG-01A-21D-A42E-08 | TCGA-ZF-A9RG-10A-01D-A42H-08 | g.chr3:73432631C>T | c.3086G>A | c.(3085-3087)aGg>aAg | p.R1029K |
| BLCA | 3 | 73432662 | 73432662 | + | Missense_Mutation | SNP | C | C | T | TCGA-CF-A3MG-01A-11D-A20D-08 | TCGA-CF-A3MG-10A-01D-A20D-08 | g.chr3:73432662C>T | c.3055G>A | c.(3055-3057)Gaa>Aaa | p.E1019K |
| BLCA | 3 | 73432680 | 73432680 | + | Missense_Mutation | SNP | T | T | G | TCGA-ZF-AA4R-01A-11D-A38G-08 | TCGA-ZF-AA4R-10A-01D-A38J-08 | g.chr3:73432680T>G | c.3037A>C | c.(3037-3039)Aag>Cag | p.K1013Q |
| BLCA | 3 | 73432821 | 73432821 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr3:73432821C>T | c.2896G>A | c.(2896-2898)Gag>Aag | p.E966K |
| BLCA | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-E7-A519-01A-11D-A26M-08 | TCGA-E7-A519-10A-01D-A26K-08 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| BLCA | 3 | 73433184 | 73433184 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3IM-01A-11D-A20D-08 | TCGA-DK-A3IM-10A-01D-A20D-08 | g.chr3:73433184C>T | c.2533G>A | c.(2533-2535)Ggg>Agg | p.G845R |
| BLCA | 3 | 73433185 | 73433185 | + | Silent | SNP | G | G | A | TCGA-CF-A3MI-01A-11D-A20D-08 | TCGA-CF-A3MI-10A-01D-A20D-08 | g.chr3:73433185G>A | c.2532C>T | c.(2530-2532)gaC>gaT | p.D844D |
| BLCA | 3 | 73433413 | 73433414 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-BL-A0C8-01A-11D-A10S-08 | TCGA-BL-A0C8-10A-01D-A10S-08 | g.chr3:73433413_73433414insG | c.2303_2304insC | c.(2302-2304)ccgfs | p.P768fs |
| BLCA | 3 | 73433466 | 73433466 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr3:73433466C>T | c.2251G>A | c.(2251-2253)Gac>Aac | p.D751N |
| BLCA | 3 | 73433676 | 73433676 | + | Missense_Mutation | SNP | C | C | A | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr3:73433676C>A | c.2041G>T | c.(2041-2043)Gtg>Ttg | p.V681L |
| BLCA | 3 | 73433738 | 73433738 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-AA6U-01A-11D-A391-08 | TCGA-DK-AA6U-10A-01D-A394-08 | g.chr3:73433738G>T | c.1979C>A | c.(1978-1980)aCc>aAc | p.T660N |
| BLCA | 3 | 73437193 | 73437193 | + | Missense_Mutation | SNP | C | C | T | TCGA-E7-A678-01A-11D-A30E-08 | TCGA-E7-A678-10A-01D-A30H-08 | g.chr3:73437193C>T | c.1444G>A | c.(1444-1446)Gaa>Aaa | p.E482K |
| BLCA | 3 | 73438983 | 73438983 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A20J-01A-11D-A14W-08 | TCGA-BT-A20J-11A-11D-A14W-08 | g.chr3:73438983C>T | c.1400G>A | c.(1399-1401)gGa>gAa | p.G467E |
| BLCA | 3 | 73453372 | 73453372 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr3:73453372C>T | c.1093G>A | c.(1093-1095)Gaa>Aaa | p.E365K |
| BRCA | 3 | 73432563 | 73432563 | + | Missense_Mutation | SNP | C | C | T | TCGA-AR-A1AV-01A-21D-A12Q-09 | TCGA-AR-A1AV-10A-01D-A12Q-09 | g.chr3:73432563C>T | c.3154G>A | c.(3154-3156)Gac>Aac | p.D1052N |
| BRCA | 3 | 73432884 | 73432884 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A03V-01A-11D-A10Y-09 | TCGA-AO-A03V-10A-01D-A110-09 | g.chr3:73432884C>T | c.2833G>A | c.(2833-2835)Gag>Aag | p.E945K |
| BRCA | 3 | 73433778 | 73433778 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A04X-01A-21W-A050-09 | TCGA-A2-A04X-10A-01W-A055-09 | g.chr3:73433778G>A | c.1939C>T | c.(1939-1941)Cgc>Tgc | p.R647C |
| BRCA | 3 | 73433945 | 73433945 | + | Missense_Mutation | SNP | T | T | C | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr3:73433945T>C | c.1772A>G | c.(1771-1773)gAc>gGc | p.D591G |
| BRCA | 3 | 73433946 | 73433946 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A0XS-01A-22D-A10G-09 | TCGA-AN-A0XS-10A-01D-A10G-09 | g.chr3:73433946C>T | c.1771G>A | c.(1771-1773)Gac>Aac | p.D591N |
| BRCA | 3 | 73453303 | 73453303 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A0YH-01A-11D-A10G-09 | TCGA-A2-A0YH-10A-01D-A10G-09 | g.chr3:73453303C>T | c.1162G>A | c.(1162-1164)Gag>Aag | p.E388K |
| BRCA | 3 | 73651605 | 73651605 | + | Missense_Mutation | SNP | T | T | C | TCGA-A2-A3Y0-01A-11D-A23C-09 | TCGA-A2-A3Y0-10A-01D-A23C-09 | g.chr3:73651605T>C | c.818A>G | c.(817-819)cAc>cGc | p.H273R |
| BRCA | 3 | 73657824 | 73657824 | + | Silent | SNP | G | G | T | TCGA-B6-A0I6-01A-11D-A128-09 | TCGA-B6-A0I6-10A-01W-A055-09 | g.chr3:73657824G>T | c.735C>A | c.(733-735)acC>acA | p.T245T |
| CESC | 3 | 73450114 | 73450114 | + | Missense_Mutation | SNP | C | C | T | TCGA-IR-A3LI-01A-11D-A20U-09 | TCGA-IR-A3LI-10A-01D-A20U-09 | g.chr3:73450114C>T | c.1213G>A | c.(1213-1215)Gac>Aac | p.D405N |
| CESC | 3 | 73453428 | 73453428 | + | Missense_Mutation | SNP | G | G | A | TCGA-FU-A40J-01A-11D-A243-09 | TCGA-FU-A40J-10A-01D-A243-09 | g.chr3:73453428G>A | c.1037C>T | c.(1036-1038)aCg>aTg | p.T346M |
| COAD | 3 | 73432614 | 73432614 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr3:73432614C>T | c.3103G>A | c.(3103-3105)Gat>Aat | p.D1035N |
| COAD | 3 | 73432618 | 73432618 | + | Missense_Mutation | SNP | G | G | C | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr3:73432618G>C | c.3099C>G | c.(3097-3099)atC>atG | p.I1033M |
| COAD | 3 | 73432689 | 73432689 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:73432689C>T | c.3028G>A | c.(3028-3030)Gat>Aat | p.D1010N |
| COAD | 3 | 73432699 | 73432699 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr3:73432699C>T | c.3018G>A | c.(3016-3018)caG>caA | p.Q1006Q |
| COAD | 3 | 73433004 | 73433004 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:73433004T>A | c.2713A>T | c.(2713-2715)Atg>Ttg | p.M905L |
| COAD | 3 | 73433011 | 73433011 | + | Silent | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr3:73433011C>T | c.2706G>A | c.(2704-2706)ctG>ctA | p.L902L |
| COAD | 3 | 73433029 | 73433029 | + | Silent | SNP | C | C | T | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr3:73433029C>T | c.2688G>A | c.(2686-2688)gcG>gcA | p.A896A |
| COAD | 3 | 73433031 | 73433031 | + | Missense_Mutation | SNP | C | C | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr3:73433031C>T | c.2686G>A | c.(2686-2688)Gcg>Acg | p.A896T |
| COAD | 3 | 73433053 | 73433053 | + | Silent | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:73433053C>T | c.2664G>A | c.(2662-2664)caG>caA | p.Q888Q |
| COAD | 3 | 73433092 | 73433092 | + | Silent | SNP | C | C | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr3:73433092C>A | c.2625G>T | c.(2623-2625)gcG>gcT | p.A875A |
| COAD | 3 | 73433107 | 73433107 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:73433107delG | c.2610delC | c.(2608-2610)cacfs | p.H870fs |
| COAD | 3 | 73433148 | 73433148 | + | Missense_Mutation | SNP | T | T | C | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:73433148T>C | c.2569A>G | c.(2569-2571)Agc>Ggc | p.S857G |
| COAD | 3 | 73433168 | 73433168 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:73433168G>A | c.2549C>T | c.(2548-2550)aCg>aTg | p.T850M |
| COAD | 3 | 73433170 | 73433170 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:73433170delG | c.2547delC | c.(2545-2547)cccfs | p.P849fs |
| COAD | 3 | 73433314 | 73433314 | + | Silent | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:73433314G>A | c.2403C>T | c.(2401-2403)taC>taT | p.Y801Y |
| COAD | 3 | 73433631 | 73433631 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr3:73433631C>T | c.2086G>A | c.(2086-2088)Gag>Aag | p.E696K |
| COAD | 3 | 73433698 | 73433698 | + | Silent | SNP | G | G | A | TCGA-DM-A285-01A-11D-A16V-10 | TCGA-DM-A285-10A-01D-A16V-10 | g.chr3:73433698G>A | c.2019C>T | c.(2017-2019)gcC>gcT | p.A673A |
| COAD | 3 | 73433700 | 73433700 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr3:73433700C>T | c.2017G>A | c.(2017-2019)Gcc>Acc | p.A673T |
| COAD | 3 | 73433788 | 73433788 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr3:73433788G>A | c.1929C>T | c.(1927-1929)tgC>tgT | p.C643C |
| COAD | 3 | 73433851 | 73433851 | + | Silent | SNP | G | G | A | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr3:73433851G>A | c.1866C>T | c.(1864-1866)aaC>aaT | p.N622N |
| COAD | 3 | 73433890 | 73433890 | + | Silent | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr3:73433890G>A | c.1827C>T | c.(1825-1827)agC>agT | p.S609S |
| COAD | 3 | 73450149 | 73450149 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:73450149G>A | c.1178C>T | c.(1177-1179)gCc>gTc | p.A393V |
| COAD | 3 | 73453541 | 73453541 | + | Silent | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:73453541G>A | c.924C>T | c.(922-924)aaC>aaT | p.N308N |
| COAD | 3 | 73657781 | 73657781 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr3:73657781C>A | c.778G>T | c.(778-780)Gga>Tga | p.G260* |
| COADREAD | 3 | 73432614 | 73432614 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr3:73432614C>T | c.3103G>A | c.(3103-3105)Gat>Aat | p.D1035N |
| COADREAD | 3 | 73432618 | 73432618 | + | Missense_Mutation | SNP | G | G | C | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr3:73432618G>C | c.3099C>G | c.(3097-3099)atC>atG | p.I1033M |
| COADREAD | 3 | 73432689 | 73432689 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:73432689C>T | c.3028G>A | c.(3028-3030)Gat>Aat | p.D1010N |
| COADREAD | 3 | 73432699 | 73432699 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr3:73432699C>T | c.3018G>A | c.(3016-3018)caG>caA | p.Q1006Q |
| COADREAD | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| COADREAD | 3 | 73432830 | 73432830 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A01L-01A-01W-A00K-09 | TCGA-AG-A01L-10A-01W-A00L-09 | g.chr3:73432830C>T | c.2887G>A | c.(2887-2889)Gcg>Acg | p.A963T |
| COADREAD | 3 | 73432900 | 73432900 | + | Silent | SNP | C | C | T | TCGA-AG-A02X-01A-01W-A00E-09 | TCGA-AG-A02X-10A-01W-A00E-09 | g.chr3:73432900C>T | c.2817G>A | c.(2815-2817)cgG>cgA | p.R939R |
| COADREAD | 3 | 73433004 | 73433004 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:73433004T>A | c.2713A>T | c.(2713-2715)Atg>Ttg | p.M905L |
| COADREAD | 3 | 73433011 | 73433011 | + | Silent | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr3:73433011C>T | c.2706G>A | c.(2704-2706)ctG>ctA | p.L902L |
| COADREAD | 3 | 73433029 | 73433029 | + | Silent | SNP | C | C | T | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr3:73433029C>T | c.2688G>A | c.(2686-2688)gcG>gcA | p.A896A |
| COADREAD | 3 | 73433031 | 73433031 | + | Missense_Mutation | SNP | C | C | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr3:73433031C>T | c.2686G>A | c.(2686-2688)Gcg>Acg | p.A896T |
| COADREAD | 3 | 73433053 | 73433053 | + | Silent | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:73433053C>T | c.2664G>A | c.(2662-2664)caG>caA | p.Q888Q |
| COADREAD | 3 | 73433092 | 73433092 | + | Silent | SNP | C | C | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr3:73433092C>A | c.2625G>T | c.(2623-2625)gcG>gcT | p.A875A |
| COADREAD | 3 | 73433107 | 73433107 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:73433107delG | c.2610delC | c.(2608-2610)cacfs | p.H870fs |
| COADREAD | 3 | 73433148 | 73433148 | + | Missense_Mutation | SNP | T | T | C | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:73433148T>C | c.2569A>G | c.(2569-2571)Agc>Ggc | p.S857G |
| COADREAD | 3 | 73433168 | 73433168 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:73433168G>A | c.2549C>T | c.(2548-2550)aCg>aTg | p.T850M |
| COADREAD | 3 | 73433170 | 73433170 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:73433170delG | c.2547delC | c.(2545-2547)cccfs | p.P849fs |
| COADREAD | 3 | 73433314 | 73433314 | + | Silent | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:73433314G>A | c.2403C>T | c.(2401-2403)taC>taT | p.Y801Y |
| COADREAD | 3 | 73433453 | 73433453 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:73433453G>A | c.2264C>T | c.(2263-2265)tCg>tTg | p.S755L |
| COADREAD | 3 | 73433631 | 73433631 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr3:73433631C>T | c.2086G>A | c.(2086-2088)Gag>Aag | p.E696K |
| COADREAD | 3 | 73433698 | 73433698 | + | Silent | SNP | G | G | A | TCGA-DM-A285-01A-11D-A16V-10 | TCGA-DM-A285-10A-01D-A16V-10 | g.chr3:73433698G>A | c.2019C>T | c.(2017-2019)gcC>gcT | p.A673A |
| COADREAD | 3 | 73433700 | 73433700 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr3:73433700C>T | c.2017G>A | c.(2017-2019)Gcc>Acc | p.A673T |
| COADREAD | 3 | 73433742 | 73433742 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3600-01A-01W-0833-10 | TCGA-AG-3600-10A-01W-0833-10 | g.chr3:73433742C>T | c.1975G>A | c.(1975-1977)Gcc>Acc | p.A659T |
| COADREAD | 3 | 73433788 | 73433788 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr3:73433788G>A | c.1929C>T | c.(1927-1929)tgC>tgT | p.C643C |
| COADREAD | 3 | 73433851 | 73433851 | + | Silent | SNP | G | G | A | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr3:73433851G>A | c.1866C>T | c.(1864-1866)aaC>aaT | p.N622N |
| COADREAD | 3 | 73433890 | 73433890 | + | Silent | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr3:73433890G>A | c.1827C>T | c.(1825-1827)agC>agT | p.S609S |
| COADREAD | 3 | 73450149 | 73450149 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:73450149G>A | c.1178C>T | c.(1177-1179)gCc>gTc | p.A393V |
| COADREAD | 3 | 73453541 | 73453541 | + | Silent | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:73453541G>A | c.924C>T | c.(922-924)aaC>aaT | p.N308N |
| COADREAD | 3 | 73657781 | 73657781 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr3:73657781C>A | c.778G>T | c.(778-780)Gga>Tga | p.G260* |
| DLBC | 3 | 73433731 | 73433731 | + | Silent | SNP | G | G | A | TCGA-FA-A82F-01A-11D-A382-10 | TCGA-FA-A82F-10A-01D-A385-10 | g.chr3:73433731G>A | c.1986C>T | c.(1984-1986)taC>taT | p.Y662Y |
| ESCA | 3 | 73433145 | 73433145 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A4OR-01A-11D-A27G-09 | TCGA-L5-A4OR-11A-11D-A27G-09 | g.chr3:73433145C>T | c.2572G>A | c.(2572-2574)Gcc>Acc | p.A858T |
| ESCA | 3 | 73433188 | 73433188 | + | Silent | SNP | G | G | A | TCGA-X8-AAAR-01A-11D-A403-09 | TCGA-X8-AAAR-10A-01D-A403-09 | g.chr3:73433188G>A | c.2529C>T | c.(2527-2529)agC>agT | p.S843S |
| ESCA | 3 | 73433779 | 73433779 | + | Silent | SNP | G | G | A | TCGA-LN-A7HY-01A-12D-A351-09 | TCGA-LN-A7HY-10A-01D-A351-09 | g.chr3:73433779G>A | c.1938C>T | c.(1936-1938)ttC>ttT | p.F646F |
| ESCA | 3 | 73453349 | 73453349 | + | Silent | SNP | C | C | T | TCGA-VR-AA4D-01A-11D-A37C-09 | TCGA-VR-AA4D-10A-01D-A37F-09 | g.chr3:73453349C>T | c.1116G>A | c.(1114-1116)aaG>aaA | p.K372K |
| ESCA | 3 | 73453350 | 73453350 | + | Missense_Mutation | SNP | T | T | A | TCGA-L5-A8NW-01A-11D-A37C-09 | TCGA-L5-A8NW-11A-11D-A37F-09 | g.chr3:73453350T>A | c.1115A>T | c.(1114-1116)aAg>aTg | p.K372M |
| ESCA | 3 | 73673724 | 73673724 | + | Missense_Mutation | SNP | C | C | T | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr3:73673724C>T | c.253G>A | c.(253-255)Gcg>Acg | p.A85T |
| ESCA | 3 | 73673769 | 73673769 | + | Missense_Mutation | SNP | G | G | A | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr3:73673769G>A | c.208C>T | c.(208-210)Ccg>Tcg | p.P70S |
| ESCA | 3 | 73673854 | 73673854 | + | Silent | SNP | G | G | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr3:73673854G>A | c.123C>T | c.(121-123)tgC>tgT | p.C41C |
| ESCA | 3 | 73673859 | 73673859 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NW-01A-11D-A37C-09 | TCGA-L5-A8NW-11A-11D-A37F-09 | g.chr3:73673859C>T | c.118G>A | c.(118-120)Ggc>Agc | p.G40S |
| GBM | 3 | 73673955 | 73673955 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-0184-01A-01D-1491-08 | TCGA-06-0184-10B-01D-1491-08 | g.chr3:73673955A>G | c.22T>C | c.(22-24)Ttc>Ctc | p.F8L |
| GBMLGG | 3 | 73432601 | 73432601 | + | Missense_Mutation | SNP | G | G | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr3:73432601G>A | c.3116C>T | c.(3115-3117)aCg>aTg | p.T1039M |
| GBMLGG | 3 | 73433161 | 73433161 | + | Missense_Mutation | SNP | G | G | C | TCGA-HT-8105-01A-11D-2395-08 | TCGA-HT-8105-10A-01D-2396-08 | g.chr3:73433161G>C | c.2556C>G | c.(2554-2556)agC>agG | p.S852R |
| GBMLGG | 3 | 73433282 | 73433282 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:73433282G>A | c.2435C>T | c.(2434-2436)aCg>aTg | p.T812M |
| GBMLGG | 3 | 73651590 | 73651590 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:73651590C>T | c.833G>A | c.(832-834)aGt>aAt | p.S278N |
| GBMLGG | 3 | 73673955 | 73673955 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-0184-01A-01D-1491-08 | TCGA-06-0184-10B-01D-1491-08 | g.chr3:73673955A>G | c.22T>C | c.(22-24)Ttc>Ctc | p.F8L |
| HNSC | 3 | 73432536 | 73432536 | + | Silent | SNP | G | G | A | TCGA-CV-A45V-01A-21D-A25D-08 | TCGA-CV-A45V-10A-01D-A25E-08 | g.chr3:73432536G>A | c.3181C>T | c.(3181-3183)Cta>Tta | p.L1061L |
| HNSC | 3 | 73432746 | 73432746 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-5323-01A-01D-1683-08 | TCGA-CQ-5323-10A-01D-1683-08 | g.chr3:73432746G>A | c.2971C>T | c.(2971-2973)Cgg>Tgg | p.R991W |
| HNSC | 3 | 73432909 | 73432909 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-6935-01A-11D-1912-08 | TCGA-CV-6935-10A-01D-1912-08 | g.chr3:73432909C>A | c.2808G>T | c.(2806-2808)agG>agT | p.R936S |
| HNSC | 3 | 73433074 | 73433074 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr3:73433074C>A | c.2643G>T | c.(2641-2643)caG>caT | p.Q881H |
| HNSC | 3 | 73433279 | 73433279 | + | Missense_Mutation | SNP | T | T | G | TCGA-CV-5432-01A-02D-1683-08 | TCGA-CV-5432-10A-01D-1870-08 | g.chr3:73433279T>G | c.2438A>C | c.(2437-2439)gAa>gCa | p.E813A |
| HNSC | 3 | 73433280 | 73433280 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr3:73433280C>T | c.2437G>A | c.(2437-2439)Gaa>Aaa | p.E813K |
| HNSC | 3 | 73433317 | 73433317 | + | Silent | SNP | G | G | T | TCGA-CN-A497-01A-11D-A24D-08 | TCGA-CN-A497-10A-01D-A24F-08 | g.chr3:73433317G>T | c.2400C>A | c.(2398-2400)gcC>gcA | p.A800A |
| HNSC | 3 | 73433465 | 73433465 | + | Missense_Mutation | SNP | T | T | C | TCGA-BA-4078-01A-01D-1434-08 | TCGA-BA-4078-10A-01D-1434-08 | g.chr3:73433465T>C | c.2252A>G | c.(2251-2253)gAc>gGc | p.D751G |
| HNSC | 3 | 73433477 | 73433477 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-4734-01A-01D-1434-08 | TCGA-CN-4734-10A-01D-1434-08 | g.chr3:73433477G>A | c.2240C>T | c.(2239-2241)cCg>cTg | p.P747L |
| HNSC | 3 | 73433507 | 73433507 | + | Missense_Mutation | SNP | C | C | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr3:73433507C>A | c.2210G>T | c.(2209-2211)aGa>aTa | p.R737I |
| HNSC | 3 | 73433788 | 73433788 | + | Silent | SNP | G | G | A | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr3:73433788G>A | c.1929C>T | c.(1927-1929)tgC>tgT | p.C643C |
| HNSC | 3 | 73433878 | 73433878 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr3:73433878C>A | c.1839G>T | c.(1837-1839)ttG>ttT | p.L613F |
| HNSC | 3 | 73433958 | 73433958 | + | Missense_Mutation | SNP | C | C | G | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr3:73433958C>G | c.1759G>C | c.(1759-1761)Gag>Cag | p.E587Q |
| HNSC | 3 | 73433986 | 73433986 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-4739-01A-02D-1512-08 | TCGA-CN-4739-10A-01D-1512-08 | g.chr3:73433986G>T | c.1731C>A | c.(1729-1731)agC>agA | p.S577R |
| HNSC | 3 | 73434064 | 73434064 | + | Silent | SNP | G | G | A | TCGA-P3-A5Q6-01A-11D-A28R-08 | TCGA-P3-A5Q6-10A-01D-A28U-08 | g.chr3:73434064G>A | c.1653C>T | c.(1651-1653)gaC>gaT | p.D551D |
| HNSC | 3 | 73437118 | 73437118 | + | Splice_Site | SNP | C | C | A | TCGA-BB-A5HY-01A-11D-A28R-08 | TCGA-BB-A5HY-10A-01D-A28U-08 | g.chr3:73437118C>A | | c.e8+1 | |
| HNSC | 3 | 73440206 | 73440206 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-5366-01A-01D-1434-08 | TCGA-CN-5366-10A-01D-1434-08 | g.chr3:73440206G>A | c.1316C>T | c.(1315-1317)aCg>aTg | p.T439M |
| HNSC | 3 | 73440229 | 73440229 | + | Silent | SNP | C | C | T | TCGA-CX-A4AQ-01A-11D-A25D-08 | TCGA-CX-A4AQ-10A-01D-A25E-08 | g.chr3:73440229C>T | c.1293G>A | c.(1291-1293)ctG>ctA | p.L431L |
| HNSC | 3 | 73450159 | 73450159 | + | Splice_Site | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr3:73450159G>A | c.1168C>T | c.(1168-1170)Cat>Tat | p.H390Y |
| HNSC | 3 | 73453527 | 73453527 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-A45Z-01A-21D-A25D-08 | TCGA-CV-A45Z-10A-01D-A25E-08 | g.chr3:73453527G>T | c.938C>A | c.(937-939)tCc>tAc | p.S313Y |
| HNSC | 3 | 73651507 | 73651507 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-6472-01A-11D-1870-08 | TCGA-CR-6472-10A-01D-1870-08 | g.chr3:73651507C>G | c.916G>C | c.(916-918)Gag>Cag | p.E306Q |
| KICH | 3 | 73657758 | 73657758 | + | Silent | SNP | C | C | G | TCGA-KL-8339-01A-11D-2310-10 | TCGA-KL-8339-11A-01D-2310-10 | g.chr3:73657758C>G | c.801G>C | c.(799-801)cgG>cgC | p.R267R |
| KIPAN | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-AL-3468-01A-01D-1252-08 | TCGA-AL-3468-10A-01D-1252-08 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| KIPAN | 3 | 73432856 | 73432856 | + | Missense_Mutation | SNP | C | C | A | TCGA-CJ-4644-01A-02D-1386-10 | TCGA-CJ-4644-11A-01D-1251-10 | g.chr3:73432856C>A | c.2861G>T | c.(2860-2862)cGc>cTc | p.R954L |
| KIPAN | 3 | 73657758 | 73657758 | + | Silent | SNP | C | C | G | TCGA-KL-8339-01A-11D-2310-10 | TCGA-KL-8339-11A-01D-2310-10 | g.chr3:73657758C>G | c.801G>C | c.(799-801)cgG>cgC | p.R267R |
| KIRC | 3 | 73432856 | 73432856 | + | Missense_Mutation | SNP | C | C | A | TCGA-CJ-4644-01A-02D-1386-10 | TCGA-CJ-4644-11A-01D-1251-10 | g.chr3:73432856C>A | c.2861G>T | c.(2860-2862)cGc>cTc | p.R954L |
| KIRP | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-AL-3468-01A-01D-1252-08 | TCGA-AL-3468-10A-01D-1252-08 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| LGG | 3 | 73432601 | 73432601 | + | Missense_Mutation | SNP | G | G | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr3:73432601G>A | c.3116C>T | c.(3115-3117)aCg>aTg | p.T1039M |
| LGG | 3 | 73433161 | 73433161 | + | Missense_Mutation | SNP | G | G | C | TCGA-HT-8105-01A-11D-2395-08 | TCGA-HT-8105-10A-01D-2396-08 | g.chr3:73433161G>C | c.2556C>G | c.(2554-2556)agC>agG | p.S852R |
| LGG | 3 | 73433282 | 73433282 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:73433282G>A | c.2435C>T | c.(2434-2436)aCg>aTg | p.T812M |
| LGG | 3 | 73651590 | 73651590 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:73651590C>T | c.833G>A | c.(832-834)aGt>aAt | p.S278N |
| LIHC | 3 | 73432795 | 73432795 | + | Missense_Mutation | SNP | G | G | T | TCGA-LG-A6GG-01A-11D-A30V-10 | TCGA-LG-A6GG-10A-01D-A30V-10 | g.chr3:73432795G>T | c.2922C>A | c.(2920-2922)agC>agA | p.S974R |
| LIHC | 3 | 73433257 | 73433257 | + | Silent | SNP | A | A | G | TCGA-EP-A2KB-01A-11D-A183-10 | TCGA-EP-A2KB-10A-01D-A183-10 | g.chr3:73433257A>G | c.2460T>C | c.(2458-2460)ccT>ccC | p.P820P |
| LIHC | 3 | 73433851 | 73433851 | + | Silent | SNP | G | G | A | TCGA-BC-A5W4-01A-11D-A28X-10 | TCGA-BC-A5W4-10A-01D-A28X-10 | g.chr3:73433851G>A | c.1866C>T | c.(1864-1866)aaC>aaT | p.N622N |
| LIHC | 3 | 73433952 | 73433952 | + | Missense_Mutation | SNP | T | T | G | TCGA-5R-AA1C-01A-11D-A40R-10 | TCGA-5R-AA1C-10A-01D-A40U-10 | g.chr3:73433952T>G | c.1765A>C | c.(1765-1767)Aat>Cat | p.N589H |
| LIHC | 3 | 73434932 | 73434932 | + | Missense_Mutation | SNP | T | T | C | TCGA-BC-A3KF-01A-11D-A20W-10 | TCGA-BC-A3KF-10A-01D-A20W-10 | g.chr3:73434932T>C | c.1523A>G | c.(1522-1524)gAt>gGt | p.D508G |
| LIHC | 3 | 73673351 | 73673351 | + | Missense_Mutation | SNP | A | A | C | TCGA-LG-A6GG-01A-11D-A30V-10 | TCGA-LG-A6GG-10A-01D-A30V-10 | g.chr3:73673351A>C | c.626T>G | c.(625-627)cTg>cGg | p.L209R |
| LIHC | 3 | 73673733 | 73673733 | + | Missense_Mutation | SNP | A | A | G | TCGA-2Y-A9GW-01A-11D-A382-10 | TCGA-2Y-A9GW-10A-01D-A385-10 | g.chr3:73673733A>G | c.244T>C | c.(244-246)Tgc>Cgc | p.C82R |
| LUAD | 3 | 73432531 | 73432531 | + | Silent | SNP | C | C | A | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr3:73432531C>A | c.3186G>T | c.(3184-3186)tcG>tcT | p.S1062S |
| LUAD | 3 | 73432630 | 73432630 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr3:73432630C>A | c.3087G>T | c.(3085-3087)agG>agT | p.R1029S |
| LUAD | 3 | 73432631 | 73432631 | + | Missense_Mutation | SNP | C | C | G | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr3:73432631C>G | c.3086G>C | c.(3085-3087)aGg>aCg | p.R1029T |
| LUAD | 3 | 73432636 | 73432636 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4405-01A-21D-1855-08 | TCGA-05-4405-10A-01D-1855-08 | g.chr3:73432636C>A | c.3081G>T | c.(3079-3081)aaG>aaT | p.K1027N |
| LUAD | 3 | 73432672 | 73432672 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5778-01A-01D-1625-08 | TCGA-64-5778-10A-01D-1625-08 | g.chr3:73432672C>A | c.3045G>T | c.(3043-3045)atG>atT | p.M1015I |
| LUAD | 3 | 73432744 | 73432744 | + | Silent | SNP | C | C | A | TCGA-MP-A4TF-01A-11D-A25L-08 | TCGA-MP-A4TF-10A-01D-A25L-08 | g.chr3:73432744C>A | c.2973G>T | c.(2971-2973)cgG>cgT | p.R991R |
| LUAD | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| LUAD | 3 | 73432837 | 73432837 | + | Missense_Mutation | SNP | G | G | T | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chr3:73432837G>T | c.2880C>A | c.(2878-2880)gaC>gaA | p.D960E |
| LUAD | 3 | 73432844 | 73432844 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr3:73432844G>T | c.2873C>A | c.(2872-2874)aCc>aAc | p.T958N |
| LUAD | 3 | 73432850 | 73432850 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr3:73432850C>A | c.2867G>T | c.(2866-2868)gGc>gTc | p.G956V |
| LUAD | 3 | 73432857 | 73432857 | + | Missense_Mutation | SNP | G | G | C | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr3:73432857G>C | c.2860C>G | c.(2860-2862)Cgc>Ggc | p.R954G |
| LUAD | 3 | 73432879 | 73432879 | + | Silent | SNP | G | G | T | TCGA-53-A4EZ-01A-12D-A24P-08 | TCGA-53-A4EZ-10A-01D-A24P-08 | g.chr3:73432879G>T | c.2838C>A | c.(2836-2838)cgC>cgA | p.R946R |
| LUAD | 3 | 73432910 | 73432910 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr3:73432910C>A | c.2807G>T | c.(2806-2808)aGg>aTg | p.R936M |
| LUAD | 3 | 73432940 | 73432940 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr3:73432940C>G | c.2777G>C | c.(2776-2778)cGc>cCc | p.R926P |
| LUAD | 3 | 73432950 | 73432950 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr3:73432950C>A | c.2767G>T | c.(2767-2769)Gtg>Ttg | p.V923L |
| LUAD | 3 | 73433080 | 73433080 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z059-01A-01W-0747-08 | TCGA-17-Z059-11A-01W-0747-08 | g.chr3:73433080G>T | c.2637C>A | c.(2635-2637)caC>caA | p.H879Q |
| LUAD | 3 | 73433087 | 73433087 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr3:73433087G>T | c.2630C>A | c.(2629-2631)gCc>gAc | p.A877D |
| LUAD | 3 | 73433089 | 73433089 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-A4DG-01A-11D-A24D-08 | TCGA-55-A4DG-10A-01D-A24F-08 | g.chr3:73433089G>T | c.2628C>A | c.(2626-2628)caC>caA | p.H876Q |
| LUAD | 3 | 73433091 | 73433091 | + | Missense_Mutation | SNP | G | G | T | TCGA-35-4123-01A-01D-1105-08 | TCGA-35-4123-10A-01D-1105-08 | g.chr3:73433091G>T | c.2626C>A | c.(2626-2628)Cac>Aac | p.H876N |
| LUAD | 3 | 73433092 | 73433092 | + | Silent | SNP | C | C | G | TCGA-53-7626-01A-12D-2063-08 | TCGA-53-7626-10A-01D-2063-08 | g.chr3:73433092C>G | c.2625G>C | c.(2623-2625)gcG>gcC | p.A875A |
| LUAD | 3 | 73433097 | 73433098 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-44-4112-01A-01D-1105-08 | TCGA-44-4112-10A-01D-1458-08 | g.chr3:73433097_73433098insA | c.2619_2620insT | c.(2617-2622)atcccgfs | p.P874fs |
| LUAD | 3 | 73433149 | 73433149 | + | Silent | SNP | G | G | T | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chr3:73433149G>T | c.2568C>A | c.(2566-2568)ggC>ggA | p.G856G |
| LUAD | 3 | 73433185 | 73433185 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr3:73433185G>T | c.2532C>A | c.(2530-2532)gaC>gaA | p.D844E |
| LUAD | 3 | 73433228 | 73433228 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z047-01A-01W-0747-08 | TCGA-17-Z047-11A-01W-0746-08 | g.chr3:73433228T>C | c.2489A>G | c.(2488-2490)gAc>gGc | p.D830G |
| LUAD | 3 | 73433282 | 73433282 | + | Missense_Mutation | SNP | G | G | T | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr3:73433282G>T | c.2435C>A | c.(2434-2436)aCg>aAg | p.T812K |
| LUAD | 3 | 73433384 | 73433384 | + | Missense_Mutation | SNP | G | G | C | TCGA-MP-A4TH-01A-31D-A25L-08 | TCGA-MP-A4TH-10A-01D-A25L-08 | g.chr3:73433384G>C | c.2333C>G | c.(2332-2334)tCc>tGc | p.S778C |
| LUAD | 3 | 73433421 | 73433421 | + | Missense_Mutation | SNP | T | T | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr3:73433421T>A | c.2296A>T | c.(2296-2298)Agc>Tgc | p.S766C |
| LUAD | 3 | 73433423 | 73433423 | + | Missense_Mutation | SNP | C | C | A | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr3:73433423C>A | c.2294G>T | c.(2293-2295)cGc>cTc | p.R765L |
| LUAD | 3 | 73433528 | 73433528 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z049-01A-01W-0746-08 | TCGA-17-Z049-11A-01W-0747-08 | g.chr3:73433528T>C | c.2189A>G | c.(2188-2190)aAc>aGc | p.N730S |
| LUAD | 3 | 73433556 | 73433556 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-5775-01A-01D-1625-08 | TCGA-64-5775-10A-01D-1625-08 | g.chr3:73433556G>T | c.2161C>A | c.(2161-2163)Ctg>Atg | p.L721M |
| LUAD | 3 | 73433717 | 73433717 | + | Missense_Mutation | SNP | G | G | A | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr3:73433717G>A | c.2000C>T | c.(1999-2001)cCt>cTt | p.P667L |
| LUAD | 3 | 73433718 | 73433718 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr3:73433718G>T | c.1999C>A | c.(1999-2001)Cct>Act | p.P667T |
| LUAD | 3 | 73433740 | 73433740 | + | Silent | SNP | G | G | T | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr3:73433740G>T | c.1977C>A | c.(1975-1977)gcC>gcA | p.A659A |
| LUAD | 3 | 73433768 | 73433768 | + | Missense_Mutation | SNP | A | A | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr3:73433768A>T | c.1949T>A | c.(1948-1950)cTg>cAg | p.L650Q |
| LUAD | 3 | 73433779 | 73433779 | + | Silent | SNP | G | G | A | TCGA-91-6830-01A-11D-1945-08 | TCGA-91-6830-11A-01D-1945-08 | g.chr3:73433779G>A | c.1938C>T | c.(1936-1938)ttC>ttT | p.F646F |
| LUAD | 3 | 73433800 | 73433800 | + | Silent | SNP | C | C | T | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr3:73433800C>T | c.1917G>A | c.(1915-1917)ccG>ccA | p.P639P |
| LUAD | 3 | 73433871 | 73433871 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-A4DF-01A-11D-A24D-08 | TCGA-55-A4DF-10A-01D-A24F-08 | g.chr3:73433871C>A | c.1846G>T | c.(1846-1848)Ggc>Tgc | p.G616C |
| LUAD | 3 | 73433873 | 73433873 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-8640-01A-11D-2393-08 | TCGA-78-8640-11A-01D-2393-08 | g.chr3:73433873C>A | c.1844G>T | c.(1843-1845)aGc>aTc | p.S615I |
| LUAD | 3 | 73433891 | 73433891 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8204-01A-11D-2238-08 | TCGA-55-8204-10A-01D-2238-08 | g.chr3:73433891C>A | c.1826G>T | c.(1825-1827)aGc>aTc | p.S609I |
| LUAD | 3 | 73433914 | 73433914 | + | Silent | SNP | C | C | T | TCGA-69-7974-01A-11D-2184-08 | TCGA-69-7974-10A-01D-2184-08 | g.chr3:73433914C>T | c.1803G>A | c.(1801-1803)gcG>gcA | p.A601A |
| LUAD | 3 | 73433919 | 73433919 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr3:73433919G>T | c.1798C>A | c.(1798-1800)Ctg>Atg | p.L600M |
| LUAD | 3 | 73434882 | 73434882 | + | Missense_Mutation | SNP | T | T | A | TCGA-69-8253-01A-11D-2284-08 | TCGA-69-8253-10A-01D-2284-08 | g.chr3:73434882T>A | c.1573A>T | c.(1573-1575)Atg>Ttg | p.M525L |
| LUAD | 3 | 73434883 | 73434883 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr3:73434883G>T | c.1572C>A | c.(1570-1572)caC>caA | p.H524Q |
| LUAD | 3 | 73437170 | 73437170 | + | Silent | SNP | G | G | C | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr3:73437170G>C | c.1467C>G | c.(1465-1467)acC>acG | p.T489T |
| LUAD | 3 | 73438977 | 73438977 | + | Missense_Mutation | SNP | C | C | T | TCGA-MP-A4TE-01A-22D-A25L-08 | TCGA-MP-A4TE-10A-01D-A25L-08 | g.chr3:73438977C>T | c.1406G>A | c.(1405-1407)cGc>cAc | p.R469H |
| LUAD | 3 | 73438989 | 73438989 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-7948-01A-11D-2184-08 | TCGA-95-7948-10A-01D-2184-08 | g.chr3:73438989C>T | c.1394G>A | c.(1393-1395)cGa>cAa | p.R465Q |
| LUAD | 3 | 73439018 | 73439018 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr3:73439018G>T | c.1365C>A | c.(1363-1365)aaC>aaA | p.N455K |
| LUAD | 3 | 73440201 | 73440201 | + | Missense_Mutation | SNP | C | C | G | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chr3:73440201C>G | c.1321G>C | c.(1321-1323)Gat>Cat | p.D441H |
| LUAD | 3 | 73440205 | 73440205 | + | Silent | SNP | C | C | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr3:73440205C>T | c.1317G>A | c.(1315-1317)acG>acA | p.T439T |
| LUAD | 3 | 73450153 | 73450153 | + | Missense_Mutation | SNP | A | A | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr3:73450153A>T | c.1174T>A | c.(1174-1176)Tca>Aca | p.S392T |
| LUAD | 3 | 73453360 | 73453360 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr3:73453360C>A | c.1105G>T | c.(1105-1107)Gcc>Tcc | p.A369S |
| LUAD | 3 | 73453385 | 73453385 | + | Silent | SNP | G | G | A | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr3:73453385G>A | c.1080C>T | c.(1078-1080)acC>acT | p.T360T |
| LUAD | 3 | 73651529 | 73651529 | + | Silent | SNP | C | C | A | TCGA-49-6744-01A-11D-1855-08 | TCGA-49-6744-11A-01D-1855-08 | g.chr3:73651529C>A | c.894G>T | c.(892-894)ctG>ctT | p.L298L |
| LUAD | 3 | 73651536 | 73651536 | + | Missense_Mutation | SNP | C | C | T | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr3:73651536C>T | c.887G>A | c.(886-888)gGa>gAa | p.G296E |
| LUAD | 3 | 73657747 | 73657747 | + | Splice_Site | SNP | A | A | G | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr3:73657747A>G | | c.e2+1 | |
| LUAD | 3 | 73657782 | 73657782 | + | Silent | SNP | C | C | A | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr3:73657782C>A | c.777G>T | c.(775-777)ctG>ctT | p.L259L |
| LUAD | 3 | 73657834 | 73657834 | + | Splice_Site | SNP | C | C | A | TCGA-44-7667-01A-31D-2063-08 | TCGA-44-7667-10A-01D-2063-08 | g.chr3:73657834C>A | c.725G>T | c.(724-726)gGc>gTc | p.G242V |
| LUAD | 3 | 73673725 | 73673725 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr3:73673725G>T | c.252C>A | c.(250-252)taC>taA | p.Y84* |
| LUAD | 3 | 73673772 | 73673772 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr3:73673772G>T | c.205C>A | c.(205-207)Ctg>Atg | p.L69M |
| LUSC | 3 | 73433190 | 73433190 | + | Missense_Mutation | SNP | T | T | C | TCGA-66-2744-01A-01D-0983-08 | TCGA-66-2744-11A-01D-0983-08 | g.chr3:73433190T>C | c.2527A>G | c.(2527-2529)Agc>Ggc | p.S843G |
| LUSC | 3 | 73433255 | 73433255 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-4721-01A-01D-1441-08 | TCGA-18-4721-11A-01D-1441-08 | g.chr3:73433255G>T | c.2462C>A | c.(2461-2463)aCc>aAc | p.T821N |
| LUSC | 3 | 73433323 | 73433323 | + | Silent | SNP | C | C | T | TCGA-21-5787-01A-01D-1632-08 | TCGA-21-5787-10A-01D-1632-08 | g.chr3:73433323C>T | c.2394G>A | c.(2392-2394)acG>acA | p.T798T |
| LUSC | 3 | 73433401 | 73433401 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2789-01A-01D-0983-08 | TCGA-66-2789-11A-01D-0983-08 | g.chr3:73433401C>A | c.2316G>T | c.(2314-2316)gaG>gaT | p.E772D |
| LUSC | 3 | 73433433 | 73433433 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-66-2794-01A-01D-1267-08 | TCGA-66-2794-11A-01D-1267-08 | g.chr3:73433433C>A | c.2284G>T | c.(2284-2286)Gag>Tag | p.E762* |
| LUSC | 3 | 73433565 | 73433565 | + | Missense_Mutation | SNP | A | A | T | TCGA-66-2768-01A-01D-1522-08 | TCGA-66-2768-11A-01D-1522-08 | g.chr3:73433565A>T | c.2152T>A | c.(2152-2154)Tcc>Acc | p.S718T |
| LUSC | 3 | 73433601 | 73433601 | + | Missense_Mutation | SNP | G | G | C | TCGA-21-5784-01A-01D-1632-08 | TCGA-21-5784-10A-01D-1632-08 | g.chr3:73433601G>C | c.2116C>G | c.(2116-2118)Cac>Gac | p.H706D |
| LUSC | 3 | 73433611 | 73433611 | + | Silent | SNP | G | G | A | TCGA-66-2791-01A-01D-0983-08 | TCGA-66-2791-11A-01D-0983-08 | g.chr3:73433611G>A | c.2106C>T | c.(2104-2106)atC>atT | p.I702I |
| LUSC | 3 | 73433635 | 73433635 | + | Silent | SNP | G | G | A | TCGA-22-5491-01A-01D-1632-08 | TCGA-22-5491-11A-01D-1632-08 | g.chr3:73433635G>A | c.2082C>T | c.(2080-2082)agC>agT | p.S694S |
| LUSC | 3 | 73437214 | 73437214 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-3406-01A-01D-0983-08 | TCGA-18-3406-11A-01D-0983-08 | g.chr3:73437214C>T | c.1423G>A | c.(1423-1425)Ggg>Agg | p.G475R |
| LUSC | 3 | 73453457 | 73453457 | + | Missense_Mutation | SNP | C | C | G | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr3:73453457C>G | c.1008G>C | c.(1006-1008)ttG>ttC | p.L336F |
| LUSC | 3 | 73673863 | 73673863 | + | Missense_Mutation | SNP | G | G | C | TCGA-33-4586-01A-01D-1441-08 | TCGA-33-4586-11A-01D-1441-08 | g.chr3:73673863G>C | c.114C>G | c.(112-114)tgC>tgG | p.C38W |
| OV | 3 | 73433881 | 73433881 | + | Silent | SNP | G | G | A | TCGA-13-1498-01A-01W-0549-09 | TCGA-13-1498-10A-01W-0549-09 | g.chr3:73433881G>A | c.1836C>T | c.(1834-1836)acC>acT | p.T612T |
| OV | 3 | 73434831 | 73434831 | + | Missense_Mutation | SNP | C | C | G | TCGA-13-0916-01A-01W-0420-08 | TCGA-13-0916-10A-01D-0399-08 | g.chr3:73434831C>G | c.1624G>C | c.(1624-1626)Gtg>Ctg | p.V542L |
| PAAD | 3 | 73432928 | 73432928 | + | Missense_Mutation | SNP | G | G | A | TCGA-XN-A8T3-01A-11D-A36O-08 | TCGA-XN-A8T3-10A-01D-A367-08 | g.chr3:73432928G>A | c.2789C>T | c.(2788-2790)aCg>aTg | p.T930M |
| PAAD | 3 | 73432936 | 73432936 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:73432936G>A | c.2781C>T | c.(2779-2781)agC>agT | p.S927S |
| PAAD | 3 | 73433199 | 73433199 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:73433199G>A | c.2518C>T | c.(2518-2520)Cgg>Tgg | p.R840W |
| PAAD | 3 | 73433317 | 73433317 | + | Silent | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:73433317G>T | c.2400C>A | c.(2398-2400)gcC>gcA | p.A800A |
| PAAD | 3 | 73433515 | 73433515 | + | Silent | SNP | G | G | A | TCGA-IB-A6UG-01A-32D-A33T-08 | TCGA-IB-A6UG-10A-01D-A33W-08 | g.chr3:73433515G>A | c.2202C>T | c.(2200-2202)gaC>gaT | p.D734D |
| PAAD | 3 | 73433639 | 73433639 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:73433639C>T | c.2078G>A | c.(2077-2079)cGc>cAc | p.R693H |
| PAAD | 3 | 73434832 | 73434832 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:73434832G>A | c.1623C>T | c.(1621-1623)agC>agT | p.S541S |
| PAAD | 3 | 73434878 | 73434878 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-A6UG-01A-32D-A33T-08 | TCGA-IB-A6UG-10A-01D-A33W-08 | g.chr3:73434878T>C | c.1577A>G | c.(1576-1578)gAc>gGc | p.D526G |
| PAAD | 3 | 73438995 | 73438995 | + | Missense_Mutation | SNP | C | C | T | TCGA-XD-AAUL-01A-21D-A397-08 | TCGA-XD-AAUL-10A-01D-A39A-08 | g.chr3:73438995C>T | c.1388G>A | c.(1387-1389)cGc>cAc | p.R463H |
| PAAD | 3 | 73440202 | 73440202 | + | Silent | SNP | G | G | A | TCGA-US-A779-01A-11D-A32N-08 | TCGA-US-A779-11A-11D-A32N-08 | g.chr3:73440202G>A | c.1320C>T | c.(1318-1320)gaC>gaT | p.D440D |
| PCPG | 3 | 73432662 | 73432662 | + | Missense_Mutation | SNP | C | C | T | TCGA-RW-A7CZ-01A-11D-A35D-08 | TCGA-RW-A7CZ-10B-01D-A35B-08 | g.chr3:73432662C>T | c.3055G>A | c.(3055-3057)Gaa>Aaa | p.E1019K |
| PRAD | 3 | 73432601 | 73432601 | + | Missense_Mutation | SNP | G | G | A | TCGA-J9-A52C-01A-11D-A26M-08 | TCGA-J9-A52C-10A-01D-A26K-08 | g.chr3:73432601G>A | c.3116C>T | c.(3115-3117)aCg>aTg | p.T1039M |
| PRAD | 3 | 73432865 | 73432865 | + | Missense_Mutation | SNP | C | C | T | TCGA-CH-5792-01A-11D-1576-08 | TCGA-CH-5792-10A-01D-1576-08 | g.chr3:73432865C>T | c.2852G>A | c.(2851-2853)cGg>cAg | p.R951Q |
| PRAD | 3 | 73432968 | 73432968 | + | Missense_Mutation | SNP | G | G | A | TCGA-CH-5794-01A-11D-1576-08 | TCGA-CH-5794-10A-01D-1577-08 | g.chr3:73432968G>A | c.2749C>T | c.(2749-2751)Ccg>Tcg | p.P917S |
| PRAD | 3 | 73433350 | 73433350 | + | Silent | SNP | C | C | T | TCGA-J9-A52C-01A-11D-A26M-08 | TCGA-J9-A52C-10A-01D-A26K-08 | g.chr3:73433350C>T | c.2367G>A | c.(2365-2367)ccG>ccA | p.P789P |
| PRAD | 3 | 73433545 | 73433545 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:73433545G>A | c.2172C>T | c.(2170-2172)agC>agT | p.S724S |
| PRAD | 3 | 73433743 | 73433743 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:73433743G>A | c.1974C>T | c.(1972-1974)agC>agT | p.S658S |
| PRAD | 3 | 73433999 | 73433999 | + | Missense_Mutation | SNP | C | C | T | TCGA-EJ-7782-01A-11D-2114-08 | TCGA-EJ-7782-10A-01D-2114-08 | g.chr3:73433999C>T | c.1718G>A | c.(1717-1719)cGg>cAg | p.R573Q |
| PRAD | 3 | 73450103 | 73450103 | + | Silent | SNP | C | C | T | TCGA-HC-A6HX-01A-11D-A31L-08 | TCGA-HC-A6HX-10A-01D-A31J-08 | g.chr3:73450103C>T | c.1224G>A | c.(1222-1224)caG>caA | p.Q408Q |
| PRAD | 3 | 73657756 | 73657756 | + | Missense_Mutation | SNP | G | G | A | TCGA-VN-A88P-01A-11D-A34U-08 | TCGA-VN-A88P-10A-01D-A34X-08 | g.chr3:73657756G>A | c.803C>T | c.(802-804)cCg>cTg | p.P268L |
| PRAD | 3 | 73657797 | 73657797 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:73657797C>T | c.762G>A | c.(760-762)cgG>cgA | p.R254R |
| READ | 3 | 73432828 | 73432828 | + | Silent | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:73432828C>T | c.2889G>A | c.(2887-2889)gcG>gcA | p.A963A |
| READ | 3 | 73432830 | 73432830 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A01L-01A-01W-A00K-09 | TCGA-AG-A01L-10A-01W-A00L-09 | g.chr3:73432830C>T | c.2887G>A | c.(2887-2889)Gcg>Acg | p.A963T |
| READ | 3 | 73432900 | 73432900 | + | Silent | SNP | C | C | T | TCGA-AG-A02X-01A-01W-A00E-09 | TCGA-AG-A02X-10A-01W-A00E-09 | g.chr3:73432900C>T | c.2817G>A | c.(2815-2817)cgG>cgA | p.R939R |
| READ | 3 | 73433453 | 73433453 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:73433453G>A | c.2264C>T | c.(2263-2265)tCg>tTg | p.S755L |
| READ | 3 | 73433742 | 73433742 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3600-01A-01W-0833-10 | TCGA-AG-3600-10A-01W-0833-10 | g.chr3:73433742C>T | c.1975G>A | c.(1975-1977)Gcc>Acc | p.A659T |
| SARC | 3 | 73433538 | 73433538 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:73433538G>A | c.2179C>T | c.(2179-2181)Cgc>Tgc | p.R727C |
| SARC | 3 | 73433539 | 73433539 | + | Silent | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:73433539G>A | c.2178C>T | c.(2176-2178)ttC>ttT | p.F726F |
| SKCM | 3 | 73432519 | 73432519 | + | Silent | SNP | T | T | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr3:73432519T>A | c.3198A>T | c.(3196-3198)gtA>gtT | p.V1066V |
| SKCM | 3 | 73432573 | 73432573 | + | Silent | SNP | T | T | C | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr3:73432573T>C | c.3144A>G | c.(3142-3144)acA>acG | p.T1048T |
| SKCM | 3 | 73432954 | 73432954 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr3:73432954C>T | c.2763G>A | c.(2761-2763)tgG>tgA | p.W921* |
| SKCM | 3 | 73433158 | 73433158 | + | Silent | SNP | C | C | T | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr3:73433158C>T | c.2559G>A | c.(2557-2559)caG>caA | p.Q853Q |
| SKCM | 3 | 73433367 | 73433367 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr3:73433367C>T | c.2350G>A | c.(2350-2352)Gag>Aag | p.E784K |
| SKCM | 3 | 73433561 | 73433561 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr3:73433561C>T | c.2156G>A | c.(2155-2157)tGg>tAg | p.W719* |
| SKCM | 3 | 73433735 | 73433735 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr3:73433735G>A | c.1982C>T | c.(1981-1983)cCt>cTt | p.P661L |
| SKCM | 3 | 73433775 | 73433775 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZA-06A-11D-A197-08 | TCGA-FS-A1ZA-10A-01D-A199-08 | g.chr3:73433775C>T | c.1942G>A | c.(1942-1944)Gag>Aag | p.E648K |
| SKCM | 3 | 73433842 | 73433842 | + | Silent | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:73433842G>A | c.1875C>T | c.(1873-1875)ttC>ttT | p.F625F |
| SKCM | 3 | 73438978 | 73438978 | + | Missense_Mutation | SNP | G | G | T | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr3:73438978G>T | c.1405C>A | c.(1405-1407)Cgc>Agc | p.R469S |
| SKCM | 3 | 73440172 | 73440172 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr3:73440172A>C | c.1350T>G | c.(1348-1350)agT>agG | p.S450R |
| SKCM | 3 | 73453318 | 73453318 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr3:73453318G>A | c.1147C>T | c.(1147-1149)Ccc>Tcc | p.P383S |