Primary Site >> Stomach Cancer
Gene >> ABCC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16036482:16036482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200485505 |
| CDS Mutation | c.688C>T |
| AA Mutation | p.Arg230Trp(p.R230W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16106758:16106758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2756C>A |
| AA Mutation | p.Ser919Tyr(p.S919Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16014596:16014596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457C>A |
| AA Mutation | p.Leu153Met(p.L153M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16141213:16141213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764004869 |
| CDS Mutation | c.4528G>A |
| AA Mutation | p.Ala1510Thr(p.A1510T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16141267:16141267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377013600 |
| CDS Mutation | c.4582G>A |
| AA Mutation | p.Ala1528Thr(p.A1528T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16138375:16138375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4304G>A |
| AA Mutation | p.Arg1435His(p.R1435H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000399410 |
| Start | 16131790:16131790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746483854 |
| CDS Mutation | c.3821C>T |
| AA Mutation | p.Ala1274Val(p.A1274V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16131817:16131817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765498811 |
| CDS Mutation | c.3848C>T |
| AA Mutation | p.Pro1283Leu(p.P1283L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16052785:16052785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1442C>A |
| AA Mutation | p.Ala481Asp(p.A481D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16111431:16111431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2928C>A |
| AA Mutation | p.Phe976Leu(p.F976L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399410 |
| Start | 16090453:16090453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754975789 |
| CDS Mutation | c.2509G>A |
| AA Mutation | p.Val837Ile(p.V837I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16122034:16122034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs4148377 |
| CDS Mutation | c.3450G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16044669:16044669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568658348 |
| CDS Mutation | c.1029G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16115022:16115022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767072123 |
| CDS Mutation | c.3336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16068194:16068194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766460837 |
| CDS Mutation | c.1716C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16033135:16033135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.642C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16124793:16124793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3595C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16138394:16138394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4323C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399410 |
| Start | 16131818:16131818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372055534 |
| CDS Mutation | c.3849G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399410 |
| Start | 16007917:16007917(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.153delC |
| AA Mutation | p.Phe52SerfsTer16(p.F52Sfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000399410 |
| Start | 16071729:16071730(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763357938 |
| CDS Mutation | c.1912+11_1912+12dupGT |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399410 |
| Start | 16048262:16048263(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1345dupC |
| AA Mutation | p.Leu449ProfsTer124(p.L449Pfs*124) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399410 |
| Start | 16007895:16007896(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.133dupT |
| AA Mutation | p.Tyr45LeufsTer17(p.Y45Lfs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |