Primary Site >> Stomach Cancer
Gene >> DIXDC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000440460 |
| Start | 111995466:111995466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782574818 |
| CDS Mutation | c.1591G>A |
| AA Mutation | p.Asp531Asn(p.D531N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000440460 |
| Start | 111996133:111996133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1743G>T |
| AA Mutation | p.Trp581Cys(p.W581C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000440460 |
| Start | 111980763:111980763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Ser228Asn(p.S228N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000440460 |
| Start | 111964639:111964639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151C>T |
| AA Mutation | p.Arg51Trp(p.R51W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000440460 |
| Start | 111985246:111985246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.933T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000440460 |
| Start | 112017819:112017819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1905T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000440460 |
| Start | 111995543:111995543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782458664 |
| CDS Mutation | c.1668G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |