Primary Site >> Stomach Cancer
Gene >> SPTLC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262554 |
| Start | 92038338:92038338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1164G>T |
| AA Mutation | p.Glu388Asp(p.E388D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262554 |
| Start | 92047259:92047259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768829356 |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Gly332Ser(p.G332S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262554 |
| Start | 92034850:92034850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143754785 |
| CDS Mutation | c.1288C>T |
| AA Mutation | p.Arg430Cys(p.R430C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262554 |
| Start | 92047267:92047267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329Gln(p.R329Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262554 |
| Start | 92046028:92046028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1107G>C |
| AA Mutation | p.Lys369Asn(p.K369N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262554 |
| Start | 92047233:92047233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377526418 |
| CDS Mutation | c.1020G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262554 |
| Start | 92047203:92047203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1050T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262554 |
| Start | 92080915:92080915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749413518 |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |