Primary Site >> Stomach Cancer
Gene >> SPNS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28981989:28981989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767378634 |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Arg300Cys(p.R300C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28982426:28982426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772584925 |
| CDS Mutation | c.1036C>T |
| AA Mutation | p.Arg346Trp(p.R346W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28982387:28982387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.997G>A |
| AA Mutation | p.Gly333Arg(p.G333R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28983795:28983795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375000927 |
| CDS Mutation | c.1330C>T |
| AA Mutation | p.Arg444Cys(p.R444C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28983837:28983837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748297241 |
| CDS Mutation | c.1372C>T |
| AA Mutation | p.Arg458Trp(p.R458W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311008 |
| Start | 28981998:28981998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.907G>A |
| AA Mutation | p.Val303Met(p.V303M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311008 |
| Start | 28984287:28984287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1575T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311008 |
| Start | 28981997:28981997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764923662 |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |