Primary Site >> Stomach Cancer
Gene >> RECK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36102212:36102212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1417C>T |
| AA Mutation | p.Pro473Ser(p.P473S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36112386:36112386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776820138 |
| CDS Mutation | c.1970G>A |
| AA Mutation | p.Arg657His(p.R657H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36108011:36108011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1612C>T |
| AA Mutation | p.Arg538Cys(p.R538C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36118813:36118813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2310T>G |
| AA Mutation | p.Ser770Arg(p.S770R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36112371:36112371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1955G>A |
| AA Mutation | p.Ser652Asn(p.S652N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36118781:36118781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141528795 |
| CDS Mutation | c.2278G>A |
| AA Mutation | p.Val760Ile(p.V760I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36087865:36087865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.809C>T |
| AA Mutation | p.Ser270Phe(p.S270F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377966 |
| Start | 36121581:36121581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746476724 |
| CDS Mutation | c.2587C>T |
| AA Mutation | p.Arg863Cys(p.R863C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377966 |
| Start | 36109991:36109991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1800C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377966 |
| Start | 36117108:36117108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2184C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377966 |
| Start | 36091290:36091290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1032A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377966 |
| Start | 36122904:36122904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757102574 |
| CDS Mutation | c.2775T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |