Primary Site >> Stomach Cancer
Gene >> ABCC8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17476731:17476731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.46C>T |
| AA Mutation | p.Arg16Trp(p.R16W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17461753:17461753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652C>A |
| AA Mutation | p.Leu218Met(p.L218M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389817 |
| Start | 17393699:17393699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772332005 |
| CDS Mutation | c.4606G>A |
| AA Mutation | p.Ala1536Thr(p.A1536T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17461759:17461759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774689517 |
| CDS Mutation | c.646C>T |
| AA Mutation | p.Arg216Cys(p.R216C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17393004:17393004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143557848 |
| CDS Mutation | c.4733G>A |
| AA Mutation | p.Arg1578His(p.R1578H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17397694:17397694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3857A>G |
| AA Mutation | p.Tyr1286Cys(p.Y1286C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17395689:17395689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4228G>A |
| AA Mutation | p.Ala1410Thr(p.A1410T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17460586:17460586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.913T>C |
| AA Mutation | p.Phe305Leu(p.F305L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17393005:17393005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147170162 |
| CDS Mutation | c.4732C>T |
| AA Mutation | p.Arg1578Cys(p.R1578C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17428312:17428312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777986828 |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Asp673Asn(p.D673N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17461591:17461591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758618229 |
| CDS Mutation | c.814G>A |
| AA Mutation | p.Ala272Thr(p.A272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17407107:17407107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2943G>T |
| AA Mutation | p.Glu981Asp(p.E981D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17407124:17407124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2926G>A |
| AA Mutation | p.Ala976Thr(p.A976T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17442863:17442863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1487T>C |
| AA Mutation | p.Leu496Pro(p.L496P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17460502:17460502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776764243 |
| CDS Mutation | c.997G>A |
| AA Mutation | p.Val333Ile(p.V333I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17476695:17476695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.82G>A |
| AA Mutation | p.Val28Met(p.V28M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17406631:17406631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3320C>T |
| AA Mutation | p.Ala1107Val(p.A1107V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17410613:17410613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2597A>G |
| AA Mutation | p.His866Arg(p.H866R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17404518:17404518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3551C>T |
| AA Mutation | p.Ala1184Val(p.A1184V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17474902:17474902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274G>T |
| AA Mutation | p.Gly92Cys(p.G92C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389817 |
| Start | 17460550:17460550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Pro317Ser(p.P317S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17396946:17396946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17402684:17402684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3627A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17428313:17428313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771361396 |
| CDS Mutation | c.2016C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17430867:17430867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1764A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17393018:17393018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772045105 |
| CDS Mutation | c.4719C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17428660:17428660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17460547:17460547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.952C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17470153:17470153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17407032:17407032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149279510 |
| CDS Mutation | c.3018C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389817 |
| Start | 17407029:17407029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556199509 |
| CDS Mutation | c.3021C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389817 |
| Start | 17412716:17412716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72559722 |
| CDS Mutation | c.2506C>T |
| AA Mutation | p.Arg836Ter(p.R836*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389817 |
| Start | 17413422:17413423(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2446dupC |
| AA Mutation | p.His816ProfsTer39(p.H816Pfs*39) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000389817 |
| Start | 17460486:17460486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1011+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000389817 |
| Start | 17404504:17404517(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3552_3557+8delGTCCAGGTGATGGC |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |