Primary Site >> Stomach Cancer
Gene >> DSC2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000280904 |
| Start | 31071839:31071839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1891A>G |
| AA Mutation | p.Thr631Ala(p.T631A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31070814:31070814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759513934 |
| CDS Mutation | c.2162C>T |
| AA Mutation | p.Thr721Met(p.T721M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31091104:31091104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398C>A |
| AA Mutation | p.Ala133Asp(p.A133D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31089473:31089473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374707462 |
| CDS Mutation | c.596G>A |
| AA Mutation | p.Arg199His(p.R199H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31089521:31089521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554713834 |
| CDS Mutation | c.548G>A |
| AA Mutation | p.Arg183Gln(p.R183Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31079896:31079896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1614G>T |
| AA Mutation | p.Glu538Asp(p.E538D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31086611:31086611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145560678 |
| CDS Mutation | c.907G>A |
| AA Mutation | p.Val303Met(p.V303M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31071644:31071644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2086G>T |
| AA Mutation | p.Ala696Ser(p.A696S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31086627:31086627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.891G>A |
| AA Mutation | p.Met297Ile(p.M297I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31080298:31080298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1318G>A |
| AA Mutation | p.Glu440Lys(p.E440K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31074757:31074757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1814G>A |
| AA Mutation | p.Gly605Asp(p.G605D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280904 |
| Start | 31091107:31091107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375410133 |
| CDS Mutation | c.395G>A |
| AA Mutation | p.Arg132His(p.R132H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280904 |
| Start | 31074864:31074864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201517977 |
| CDS Mutation | c.1707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |