Primary Site >> Stomach Cancer
Gene >> RAD52
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358495 |
| Start | 913981:913981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1108A>T |
| AA Mutation | p.Thr370Ser(p.T370S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358495 |
| Start | 913897:913897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1192A>G |
| AA Mutation | p.Thr398Ala(p.T398A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358495 |
| Start | 916350:916350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859A>G |
| AA Mutation | p.Ser287Gly(p.S287G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358495 |
| Start | 914448:914448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950T>C |
| AA Mutation | p.Val317Ala(p.V317A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358495 |
| Start | 916363:916363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765891551 |
| CDS Mutation | c.846G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358495 |
| Start | 927225:927225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358495 |
| Start | 916447:916447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199595727 |
| CDS Mutation | c.762G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358495 |
| Start | 929824:929824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144619978 |
| CDS Mutation | c.343C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |