Primary Site >> Stomach Cancer
Gene >> CYLD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50779799:50779799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1273A>G |
| AA Mutation | p.Lys425Glu(p.K425E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50751874:50751874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775G>A |
| AA Mutation | p.Glu259Lys(p.E259K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50751775:50751775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763792744 |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Glu226Lys(p.E226K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50779939:50779939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1413A>T |
| AA Mutation | p.Glu471Asp(p.E471D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50777875:50777875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1072T>G |
| AA Mutation | p.Leu358Val(p.L358V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50750105:50750105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407G>T |
| AA Mutation | p.Arg136Ile(p.R136I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50784439:50784439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1937A>C |
| AA Mutation | p.Asn646Thr(p.N646T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50796483:50796483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2846G>A |
| AA Mutation | p.Ser949Asn(p.S949N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50780000:50780000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Gly492Ser(p.G492S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50796342:50796342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2705A>T |
| AA Mutation | p.Asn902Ile(p.N902I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50796381:50796381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2744A>G |
| AA Mutation | p.Tyr915Cys(p.Y915C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50792621:50792621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2266A>C |
| AA Mutation | p.Met756Leu(p.M756L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50791666:50791666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2217C>G |
| AA Mutation | p.Ile739Met(p.I739M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311559 |
| Start | 50749843:50749843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145T>C |
| AA Mutation | p.Tyr49His(p.Y49H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311559 |
| Start | 50781377:50781377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748503826 |
| CDS Mutation | c.1650G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311559 |
| Start | 50794277:50794277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2535C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311559 |
| Start | 50751681:50751681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201431389 |
| CDS Mutation | c.582C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000311559 |
| Start | 50791608:50791608(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2165delA |
| AA Mutation | p.Asn722MetfsTer13(p.N722Mfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000311559 |
| Start | 50792627:50792627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908388 |
| CDS Mutation | c.2272C>T |
| AA Mutation | p.Arg758Ter(p.R758*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000311559 |
| Start | 50794429:50794429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2686+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |