Primary Site >> Stomach Cancer
Gene >> RUVBL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128082552:128082552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1142C>T |
| AA Mutation | p.Thr381Met(p.T381M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128097364:128097364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.952G>A |
| AA Mutation | p.Ala318Thr(p.A318T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128104850:128104850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436C>T |
| AA Mutation | p.Pro146Ser(p.P146S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128123679:128123679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200468252 |
| CDS Mutation | c.46G>A |
| AA Mutation | p.Ala16Thr(p.A16T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128112894:128112894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.355G>A |
| AA Mutation | p.Ala119Thr(p.A119T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128087741:128087741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546455182 |
| CDS Mutation | c.1084C>T |
| AA Mutation | p.Arg362Trp(p.R362W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128097408:128097408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908A>G |
| AA Mutation | p.Glu303Gly(p.E303G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128112908:128112908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.341A>G |
| AA Mutation | p.Glu114Gly(p.E114G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128097367:128097367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Arg317Cys(p.R317C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128097456:128097456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860T>C |
| AA Mutation | p.Ile287Thr(p.I287T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322623 |
| Start | 128082562:128082562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132C>T |
| AA Mutation | p.Arg378Cys(p.R378C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322623 |
| Start | 128100661:128100661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778413732 |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |