Primary Site >> Stomach Cancer
Gene >> GSR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30684144:30684144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142840135 |
| CDS Mutation | c.1097A>G |
| AA Mutation | p.Asn366Ser(p.N366S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30693051:30693051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800T>A |
| AA Mutation | p.Leu267His(p.L267H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30689199:30689199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767042164 |
| CDS Mutation | c.1003C>T |
| AA Mutation | p.Arg335Trp(p.R335W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30682028:30682028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754732491 |
| CDS Mutation | c.1187G>A |
| AA Mutation | p.Arg396Gln(p.R396Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30703174:30703174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559A>G |
| AA Mutation | p.Ser187Gly(p.S187G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221130 |
| Start | 30708125:30708125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150594097 |
| CDS Mutation | c.439C>T |
| AA Mutation | p.Arg147Trp(p.R147W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221130 |
| Start | 30682033:30682033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1182C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221130 |
| Start | 30684143:30684143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138286932 |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |