Primary Site >> Stomach Cancer
Gene >> DSG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257192 |
| Start | 31339941:31339941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1603G>A |
| AA Mutation | p.Gly535Arg(p.G535R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257192 |
| Start | 31334114:31334114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371165240 |
| CDS Mutation | c.917T>C |
| AA Mutation | p.Val306Ala(p.V306A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257192 |
| Start | 31346019:31346019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1921G>A |
| AA Mutation | p.Glu641Lys(p.E641K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257192 |
| Start | 31355214:31355214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3018G>T |
| AA Mutation | p.Leu1006Phe(p.L1006F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257192 |
| Start | 31354877:31354877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2681T>G |
| AA Mutation | p.Val894Gly(p.V894G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257192 |
| Start | 31334061:31334061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760320030 |
| CDS Mutation | c.864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257192 |
| Start | 31333594:31333594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781133396 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257192 |
| Start | 31354635:31354635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2439C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257192 |
| Start | 31338417:31338417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150549762 |
| CDS Mutation | c.1368C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |