Primary Site >> Stomach Cancer
Gene >> SYT7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61551433:61551433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Val56Met(p.V56M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61556160:61556160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.79A>C |
| AA Mutation | p.Ser27Arg(p.S27R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61527960:61527960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.577C>T |
| AA Mutation | p.Arg193Trp(p.R193W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61533006:61533006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334A>G |
| AA Mutation | p.Thr112Ala(p.T112A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61527959:61527959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.578G>A |
| AA Mutation | p.Arg193Gln(p.R193Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61551393:61551393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.206A>C |
| AA Mutation | p.Lys69Thr(p.K69T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61528161:61528161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Glu126Lys(p.E126K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263846 |
| Start | 61523217:61523217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965C>T |
| AA Mutation | p.Thr322Met(p.T322M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263846 |
| Start | 61523171:61523171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757564720 |
| CDS Mutation | c.1011C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |