Primary Site >> Stomach Cancer
Gene >> ABCG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88131192:88131192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.400C>G |
| AA Mutation | p.Leu134Val(p.L134V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88131101:88131101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Val164Ala(p.V164A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88092302:88092302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751279458 |
| CDS Mutation | c.1900G>A |
| AA Mutation | p.Ala634Thr(p.A634T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88099401:88099401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1415G>A |
| AA Mutation | p.Gly472Glu(p.G472E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88118133:88118133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.817G>T |
| AA Mutation | p.Ala273Ser(p.A273S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88113404:88113404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1093A>G |
| AA Mutation | p.Lys365Glu(p.K365E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237612 |
| Start | 88118121:88118121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.829T>G |
| AA Mutation | p.Phe277Val(p.F277V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237612 |
| Start | 88113438:88113438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774897067 |
| CDS Mutation | c.1059C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237612 |
| Start | 88115045:88115045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.855G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237612 |
| Start | 88107208:88107208(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1253delA |
| AA Mutation | p.Asn418MetfsTer16(p.N418Mfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237612 |
| Start | 88131119:88131119(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.473delA |
| AA Mutation | p.Asn158ThrfsTer11(p.N158Tfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237612 |
| Start | 88131118:88131119(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs767454866 |
| CDS Mutation | c.473dupA |
| AA Mutation | p.Asn158LysfsTer5(p.N158Kfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |