Primary Site >> Stomach Cancer
Gene >> ALPI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232457584:232457584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758457956 |
| CDS Mutation | c.668G>A |
| AA Mutation | p.Arg223His(p.R223H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458992:232458992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433C>T |
| AA Mutation | p.Ala478Val(p.A478V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232457191:232457191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372014965 |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Ala173Thr(p.A173T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458019:232458019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554429184 |
| CDS Mutation | c.878C>T |
| AA Mutation | p.Thr293Met(p.T293M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458884:232458884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325C>T |
| AA Mutation | p.Ala442Val(p.A442V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232457817:232457817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806G>A |
| AA Mutation | p.Arg269His(p.R269H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458722:232458722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1274G>A |
| AA Mutation | p.Arg425Gln(p.R425Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458109:232458109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374647501 |
| CDS Mutation | c.968G>A |
| AA Mutation | p.Arg323His(p.R323H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458900:232458900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1341G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458122:232458122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.981C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295463 |
| Start | 232456461:232456461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768884728 |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295463 |
| Start | 232458696:232458696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144515683 |
| CDS Mutation | c.1248G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |