Primary Site >> Stomach Cancer
Gene >> RAB40C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248139 |
| Start | 627527:627527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145997805 |
| CDS Mutation | c.751G>A |
| AA Mutation | p.Gly251Ser(p.G251S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248139 |
| Start | 626026:626026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470C>A |
| AA Mutation | p.Pro157His(p.P157H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248139 |
| Start | 625439:625439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272T>G |
| AA Mutation | p.Leu91Arg(p.L91R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248139 |
| Start | 618205:618205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.209C>T |
| AA Mutation | p.Thr70Met(p.T70M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248139 |
| Start | 626075:626075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756816738 |
| CDS Mutation | c.519C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248139 |
| Start | 626060:626060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777343433 |
| CDS Mutation | c.504G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248139 |
| Start | 617245:617245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.180C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248139 |
| Start | 627598:627598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545420040 |
| CDS Mutation | c.822G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000248139 |
| Start | 627580:627580(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.811delC |
| AA Mutation | p.Gln271ArgfsTer58(p.Q271Rfs*58) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000248139 |
| Start | 627579:627580(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769795950 |
| CDS Mutation | c.811dupC |
| AA Mutation | p.Gln271ProfsTer7(p.Q271Pfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |