Primary Site >> Stomach Cancer
Gene >> RAD51D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345365 |
| Start | 35101228:35101228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.876G>T |
| AA Mutation | p.Met292Ile(p.M292I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345365 |
| Start | 35101205:35101205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761290755 |
| CDS Mutation | c.899G>A |
| AA Mutation | p.Arg300Gln(p.R300Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345365 |
| Start | 35107035:35107035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755173206 |
| CDS Mutation | c.433C>T |
| AA Mutation | p.Arg145Cys(p.R145C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345365 |
| Start | 35101225:35101225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368209468 |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000345365 |
| Start | 35118615:35118626(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.145-7_149delTTGGCAGGCCCT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |