Primary Site >> Stomach Cancer
Gene >> ABCB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87426883:87426883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775186230 |
| CDS Mutation | c.1931T>A |
| AA Mutation | p.Leu644Gln(p.L644Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87475428:87475428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.38G>A |
| AA Mutation | p.Arg13His(p.R13H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87475417:87475417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.49G>A |
| AA Mutation | p.Ala17Thr(p.A17T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87462862:87462862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.182C>T |
| AA Mutation | p.Thr61Ile(p.T61I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87409243:87409243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3074T>C |
| AA Mutation | p.Leu1025Pro(p.L1025P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87408074:87408074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3242T>G |
| AA Mutation | p.Leu1081Arg(p.L1081R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87423940:87423940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141677867 |
| CDS Mutation | c.2177C>T |
| AA Mutation | p.Pro726Leu(p.P726L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87475429:87475429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753551693 |
| CDS Mutation | c.37C>T |
| AA Mutation | p.Arg13Cys(p.R13C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87420023:87420023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2369T>C |
| AA Mutation | p.Met790Thr(p.M790T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87462789:87462789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.255T>G |
| AA Mutation | p.Phe85Leu(p.F85L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87462879:87462879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.165G>T |
| AA Mutation | p.Leu55Phe(p.L55F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265723 |
| Start | 87420074:87420074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2318G>A |
| AA Mutation | p.Gly773Asp(p.G773D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87443369:87443369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1306A>G |
| AA Mutation | p.Ser436Gly(p.S436G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87417427:87417427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2567T>C |
| AA Mutation | p.Leu856Ser(p.L856S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87408047:87408047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143392573 |
| CDS Mutation | c.3269C>T |
| AA Mutation | p.Ala1090Val(p.A1090V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87439742:87439742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1656G>C |
| AA Mutation | p.Lys552Asn(p.K552N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87431496:87431496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1801G>A |
| AA Mutation | p.Ala601Thr(p.A601T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87472662:87472662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.94A>G |
| AA Mutation | p.Lys32Glu(p.K32E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87439774:87439774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140631210 |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Ala542Thr(p.A542T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87447099:87447099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.940C>A |
| AA Mutation | p.Leu314Met(p.L314M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265723 |
| Start | 87443763:87443763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1130T>A |
| AA Mutation | p.Ile377Asn(p.I377N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87406426:87406426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3369T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87406444:87406444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3351T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87451632:87451632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.699T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87423939:87423939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200740242 |
| CDS Mutation | c.2178G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87443762:87443762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1131T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87408058:87408058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3258C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265723 |
| Start | 87403156:87403156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3633T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265723 |
| Start | 87443752:87443752(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1141delT |
| AA Mutation | p.Ser381GlnfsTer32(p.S381Qfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000265723 |
| Start | 87403136:87403136(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3653delA |
| AA Mutation | p.Lys1218ArgfsTer18(p.K1218Rfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265723 |
| Start | 87444966:87444966(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753104429 |
| CDS Mutation | c.1015delT |
| AA Mutation | p.Ser339GlnfsTer3(p.S339Qfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265723 |
| Start | 87406453:87406453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3342G>A |
| AA Mutation | p.Trp1114Ter(p.W1114*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265723 |
| Start | 87462905:87462905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376926391 |
| CDS Mutation | c.139C>T |
| AA Mutation | p.Arg47Ter(p.R47*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265723 |
| Start | 87403209:87403209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3580C>T |
| AA Mutation | p.Arg1194Ter(p.R1194*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265723 |
| Start | 87422135:87422136(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.2301dupT |
| AA Mutation | p.Thr768TyrfsTer26(p.T768Yfs*26) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000265723 |
| Start | 87402098:87402098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754770911 |
| CDS Mutation | c.3859T>C |
| AA Mutation | p.Ter1287ArgextTer?(p.*1287Rext*?) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |