Primary Site >> Stomach Cancer
Gene >> SRF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265354 |
| Start | 43175848:43175848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.923C>T |
| AA Mutation | p.Ala308Val(p.A308V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265354 |
| Start | 43175853:43175853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.928G>A |
| AA Mutation | p.Val310Ile(p.V310I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265354 |
| Start | 43178383:43178383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1252G>A |
| AA Mutation | p.Ala418Thr(p.A418T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265354 |
| Start | 43174018:43174018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.685G>A |
| AA Mutation | p.Asp229Asn(p.D229N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265354 |
| Start | 43173867:43173867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142020494 |
| CDS Mutation | c.534G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265354 |
| Start | 43178319:43178319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537102728 |
| CDS Mutation | c.1188G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265354 |
| Start | 43175793:43175793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.868C>T |
| AA Mutation | p.Gln290Ter(p.Q290*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265354 |
| Start | 43175924:43175925(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1004dupG |
| AA Mutation | p.Leu336ProfsTer39(p.L336Pfs*39) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |