Primary Site >> Stomach Cancer
Gene >> DSG3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31458511:31458511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.283C>T |
| AA Mutation | p.Pro95Ser(p.P95S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31472332:31472332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1946G>A |
| AA Mutation | p.Gly649Glu(p.G649E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31456468:31456468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747138640 |
| CDS Mutation | c.77G>A |
| AA Mutation | p.Arg26Gln(p.R26Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31475892:31475892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753295246 |
| CDS Mutation | c.2632G>A |
| AA Mutation | p.Gly878Ser(p.G878S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31460848:31460848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772960249 |
| CDS Mutation | c.700C>T |
| AA Mutation | p.Arg234Cys(p.R234C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31474136:31474136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61730313 |
| CDS Mutation | c.2117C>T |
| AA Mutation | p.Thr706Met(p.T706M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31457119:31457119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211G>T |
| AA Mutation | p.Ala71Ser(p.A71S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31458577:31458577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.349C>T |
| AA Mutation | p.Arg117Trp(p.R117W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31459982:31459982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779202575 |
| CDS Mutation | c.655C>T |
| AA Mutation | p.Arg219Cys(p.R219C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257189 |
| Start | 31469191:31469191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755487489 |
| CDS Mutation | c.1739G>A |
| AA Mutation | p.Arg580His(p.R580H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257189 |
| Start | 31458513:31458513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577530234 |
| CDS Mutation | c.285G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257189 |
| Start | 31464122:31464122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113083364 |
| CDS Mutation | c.1011T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |