Primary Site >> Stomach Cancer
Gene >> AATF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619387 |
| Start | 37056644:37056644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114527666 |
| CDS Mutation | c.1663G>A |
| AA Mutation | p.Asp555Asn(p.D555N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619387 |
| Start | 36990838:36990838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1379A>T |
| AA Mutation | p.Asp460Val(p.D460V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619387 |
| Start | 37020960:37020960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368531596 |
| CDS Mutation | c.1493G>A |
| AA Mutation | p.Arg498Gln(p.R498Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000619387 |
| Start | 36950403:36950403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.281C>T |
| AA Mutation | p.Ser94Phe(p.S94F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619387 |
| Start | 36950339:36950339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.217G>A |
| AA Mutation | p.Gly73Ser(p.G73S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619387 |
| Start | 36953112:36953112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.510T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619387 |
| Start | 36989285:36989285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1188C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619387 |
| Start | 36949143:36949143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619387 |
| Start | 36988705:36988705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1134T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |