Primary Site >> Stomach Cancer
Gene >> TEP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20384088:20384088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3484A>G |
| AA Mutation | p.Arg1162Gly(p.R1162G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20381607:20381607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4504C>T |
| AA Mutation | p.Arg1502Cys(p.R1502C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262715 |
| Start | 20378981:20378981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773475088 |
| CDS Mutation | c.5252G>A |
| AA Mutation | p.Arg1751Gln(p.R1751Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20377335:20377335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6033C>A |
| AA Mutation | p.Phe2011Leu(p.F2011L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20381929:20381929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61739723 |
| CDS Mutation | c.4408G>A |
| AA Mutation | p.Val1470Ile(p.V1470I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20374505:20374505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6395T>C |
| AA Mutation | p.Leu2132Pro(p.L2132P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20386606:20386606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2702T>G |
| AA Mutation | p.Leu901Arg(p.L901R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20379940:20379940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5117G>T |
| AA Mutation | p.Arg1706Ile(p.R1706I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20380418:20380418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4820G>A |
| AA Mutation | p.Arg1607His(p.R1607H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20386490:20386490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775493633 |
| CDS Mutation | c.2818G>A |
| AA Mutation | p.Asp940Asn(p.D940N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373297:20373297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141830967 |
| CDS Mutation | c.6787C>T |
| AA Mutation | p.Arg2263Trp(p.R2263W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20380957:20380957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771792941 |
| CDS Mutation | c.4736G>A |
| AA Mutation | p.Arg1579Gln(p.R1579Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20391690:20391690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2006A>G |
| AA Mutation | p.His669Arg(p.H669R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20377336:20377336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6032T>C |
| AA Mutation | p.Phe2011Ser(p.F2011S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20378142:20378142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5603T>G |
| AA Mutation | p.Leu1868Arg(p.L1868R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20391648:20391648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2048T>C |
| AA Mutation | p.Leu683Pro(p.L683P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20385066:20385066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3026T>C |
| AA Mutation | p.Val1009Ala(p.V1009A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20403833:20403833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377196077 |
| CDS Mutation | c.1084C>T |
| AA Mutation | p.Arg362Cys(p.R362C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20384132:20384132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779605418 |
| CDS Mutation | c.3440G>A |
| AA Mutation | p.Arg1147His(p.R1147H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20386618:20386618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2690G>A |
| AA Mutation | p.Arg897His(p.R897H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20378764:20378764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759188342 |
| CDS Mutation | c.5342G>T |
| AA Mutation | p.Gly1781Val(p.G1781V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20395901:20395901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708C>A |
| AA Mutation | p.His570Asn(p.H570N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20381378:20381378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371466757 |
| CDS Mutation | c.4582G>A |
| AA Mutation | p.Ala1528Thr(p.A1528T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373704:20373704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6578G>A |
| AA Mutation | p.Cys2193Tyr(p.C2193Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20372821:20372821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6988G>A |
| AA Mutation | p.Ala2330Thr(p.A2330T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20391660:20391660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2036T>G |
| AA Mutation | p.Val679Gly(p.V679G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20372823:20372823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6986C>T |
| AA Mutation | p.Ser2329Leu(p.S2329L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20403779:20403779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1138T>C |
| AA Mutation | p.Tyr380His(p.Y380H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20395582:20395582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1796C>A |
| AA Mutation | p.Thr599Asn(p.T599N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20368472:20368472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7849G>A |
| AA Mutation | p.Val2617Met(p.V2617M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20382634:20382634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4129C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20378826:20378826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5280C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20382635:20382635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20383527:20383527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3828G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20408212:20408212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20383551:20383551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3804T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20381004:20381004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4689C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20403819:20403819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1098G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373316:20373316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6768C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262715 |
| Start | 20384614:20384614(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3207delG |
| AA Mutation | p.Ile1070SerfsTer37(p.I1070Sfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262715 |
| Start | 20369564:20369564(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7436delT |
| AA Mutation | p.Leu2479CysfsTer67(p.L2479Cfs*67) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262715 |
| Start | 20384068:20384068(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3504delG |
| AA Mutation | p.Gln1169SerfsTer28(p.Q1169Sfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262715 |
| Start | 20377481:20377481(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5887delG |
| AA Mutation | p.Ala1963LeufsTer16(p.A1963Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262715 |
| Start | 20378179:20378179(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754702761 |
| CDS Mutation | c.5566delG |
| AA Mutation | p.Val1856LeufsTer45(p.V1856Lfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |