Primary Site >> Stomach Cancer
Gene >> SLMAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428312 |
| Start | 57757817:57757817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Ala56Thr(p.A56T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428312 |
| Start | 57757829:57757829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178T>G |
| AA Mutation | p.Phe60Val(p.F60V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000428312 |
| Start | 57862086:57862086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966G>T |
| AA Mutation | p.Lys322Asn(p.K322N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428312 |
| Start | 57912591:57912591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1859G>A |
| AA Mutation | p.Arg620Gln(p.R620Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428312 |
| Start | 57912685:57912685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1953A>C |
| AA Mutation | p.Glu651Asp(p.E651D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428312 |
| Start | 57890054:57890054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139832644 |
| CDS Mutation | c.1263C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428312 |
| Start | 57831448:57831448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.264C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428312 |
| Start | 57757744:57757744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144914455 |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428312 |
| Start | 57927358:57927358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768374166 |
| CDS Mutation | c.2457C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428312 |
| Start | 57927385:57927385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753818586 |
| CDS Mutation | c.2484A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000428312 |
| Start | 57861949:57861949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746429794 |
| CDS Mutation | c.829C>T |
| AA Mutation | p.Arg277Ter(p.R277*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |