Primary Site >> Stomach Cancer
Gene >> SCD5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319540 |
| Start | 82631461:82631461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859T>G |
| AA Mutation | p.Phe287Val(p.F287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319540 |
| Start | 82798414:82798414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777230906 |
| CDS Mutation | c.124C>T |
| AA Mutation | p.Arg42Trp(p.R42W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319540 |
| Start | 82798359:82798359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.179C>T |
| AA Mutation | p.Ala60Val(p.A60V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319540 |
| Start | 82680901:82680901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319540 |
| Start | 82631420:82631420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769092388 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319540 |
| Start | 82705304:82705304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772216954 |
| CDS Mutation | c.342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000319540 |
| Start | 82636758:82636758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.635G>A |
| AA Mutation | p.Trp212Ter(p.W212*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |