Primary Site >> Stomach Cancer
Gene >> GFI1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294702 |
| Start | 92482872:92482872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.290C>T |
| AA Mutation | p.Ala97Val(p.A97V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294702 |
| Start | 92483469:92483469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19G>A |
| AA Mutation | p.Val7Ile(p.V7I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294702 |
| Start | 92476054:92476054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770564130 |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Arg415Gln(p.R415Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294702 |
| Start | 92476048:92476048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777241871 |
| CDS Mutation | c.1250C>T |
| AA Mutation | p.Thr417Met(p.T417M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294702 |
| Start | 92481056:92481056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.331G>A |
| AA Mutation | p.Glu111Lys(p.E111K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294702 |
| Start | 92481012:92481012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754401447 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |