Primary Site >> Stomach Cancer
Gene >> ERCC5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102866296:102866296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2234C>T |
| AA Mutation | p.Ala745Val(p.A745V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102862824:102862824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1675T>G |
| AA Mutation | p.Ser559Ala(p.S559A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102853836:102853836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344A>G |
| AA Mutation | p.Lys115Arg(p.K115R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102856091:102856091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.507G>A |
| AA Mutation | p.Met169Ile(p.M169I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102861583:102861583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.749T>C |
| AA Mutation | p.Val250Ala(p.V250A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102862258:102862258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370885325 |
| CDS Mutation | c.1109G>A |
| AA Mutation | p.Arg370His(p.R370H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102875875:102875875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188710607 |
| CDS Mutation | c.3533G>A |
| AA Mutation | p.Arg1178His(p.R1178H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355739 |
| Start | 102865901:102865901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2189A>G |
| AA Mutation | p.Asp730Gly(p.D730G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355739 |
| Start | 102862490:102862490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544974963 |
| CDS Mutation | c.1341G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |