Primary Site >> Stomach Cancer
Gene >> SMPD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371584:68371584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149257689 |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Val200Ile(p.V200I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68361655:68361655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1814G>A |
| AA Mutation | p.Arg605His(p.R605H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371388:68371388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Gly265Asp(p.G265D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371638:68371638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746072742 |
| CDS Mutation | c.544G>A |
| AA Mutation | p.Ala182Thr(p.A182T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371020:68371020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368965574 |
| CDS Mutation | c.1162G>A |
| AA Mutation | p.Asp388Asn(p.D388N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68372139:68372139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746300543 |
| CDS Mutation | c.43G>A |
| AA Mutation | p.Ala15Thr(p.A15T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68372045:68372045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778688383 |
| CDS Mutation | c.137G>A |
| AA Mutation | p.Arg46His(p.R46H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371692:68371692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Trp(p.R164W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371051:68371051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1131G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371480:68371480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.702C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219334 |
| Start | 68371387:68371387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219334 |
| Start | 68372041:68372041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754728453 |
| CDS Mutation | c.141G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |