Primary Site >> Stomach Cancer
Gene >> ABCC5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183925653:183925653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4114A>G |
| AA Mutation | p.Ile1372Val(p.I1372V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183942774:183942774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3647C>T |
| AA Mutation | p.Thr1216Met(p.T1216M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183982800:183982800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799A>T |
| AA Mutation | p.Asn267Tyr(p.N267Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183987800:183987800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.561G>A |
| AA Mutation | p.Met187Ile(p.M187I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183987855:183987855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506G>T |
| AA Mutation | p.Arg169Met(p.R169M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183971756:183971756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1568C>T |
| AA Mutation | p.Ser523Phe(p.S523F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183963567:183963567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2053C>A |
| AA Mutation | p.Leu685Met(p.L685M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183981832:183981832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761217800 |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Val348Met(p.V348M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334444 |
| Start | 183971720:183971720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550542220 |
| CDS Mutation | c.1604G>A |
| AA Mutation | p.Arg535His(p.R535H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183965188:183965188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758835113 |
| CDS Mutation | c.2028G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183950049:183950049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3021C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183942830:183942830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377172194 |
| CDS Mutation | c.3591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183951541:183951541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2844T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183942866:183942866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3555T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183981833:183981833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334444 |
| Start | 183950082:183950082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111257210 |
| CDS Mutation | c.2988C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334444 |
| Start | 183947469:183947469(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs762628168 |
| CDS Mutation | c.3269delT |
| AA Mutation | p.Leu1090CysfsTer26(p.L1090Cfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334444 |
| Start | 183967702:183967702(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1826delT |
| AA Mutation | p.Leu609Ter(p.L609*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |