Primary Site >> Stomach Cancer
Gene >> GAS6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327773 |
| Start | 113832671:113832671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767016321 |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Val306Met(p.V306M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327773 |
| Start | 113834651:113834651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Gly245Asp(p.G245D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000327773 |
| Start | 113823548:113823548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776678863 |
| CDS Mutation | c.1480C>T |
| AA Mutation | p.Arg494Trp(p.R494W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327773 |
| Start | 113832737:113832737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200207558 |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Val284Met(p.V284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327773 |
| Start | 113828582:113828582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1273G>A |
| AA Mutation | p.Gly425Ser(p.G425S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327773 |
| Start | 113820976:113820976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1925G>A |
| AA Mutation | p.Gly642Asp(p.G642D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327773 |
| Start | 113832386:113832386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377242538 |
| CDS Mutation | c.1056C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327773 |
| Start | 113822130:113822130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752912172 |
| CDS Mutation | c.1710C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327773 |
| Start | 113832452:113832452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747914644 |
| CDS Mutation | c.990C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327773 |
| Start | 113823432:113823432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201938938 |
| CDS Mutation | c.1596C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000327773 |
| Start | 113839745:113839745(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.449delG |
| AA Mutation | p.Gly150AlafsTer49(p.G150Afs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000327773 |
| Start | 113820885:113820885(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766199351 |
| CDS Mutation | c.2016delC |
| AA Mutation | p.Val673TrpfsTer85(p.V673Wfs*85) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000327773 |
| Start | 113839826:113839826(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.368delA |
| AA Mutation | p.Asn123ThrfsTer76(p.N123Tfs*76) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |