Primary Site >> Stomach Cancer
Gene >> SPRY4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314745:142314745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.364G>A |
| AA Mutation | p.Asp122Asn(p.D122N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314497:142314497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.612G>T |
| AA Mutation | p.Gln204His(p.Q204H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314382:142314382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201009569 |
| CDS Mutation | c.727G>A |
| AA Mutation | p.Val243Met(p.V243M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314811:142314811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.298A>G |
| AA Mutation | p.Ser100Gly(p.S100G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314879:142314879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774674946 |
| CDS Mutation | c.230C>T |
| AA Mutation | p.Thr77Met(p.T77M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314830:142314830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191016741 |
| CDS Mutation | c.279C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000434127 |
| Start | 142314632:142314632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776845832 |
| CDS Mutation | c.477C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |