Primary Site >> Stomach Cancer
Gene >> SLC5A8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101162030:101162030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1574G>A |
| AA Mutation | p.Ser525Asn(p.S525N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101190504:101190504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.797G>A |
| AA Mutation | p.Arg266Lys(p.R266K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101195138:101195138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777115655 |
| CDS Mutation | c.494C>T |
| AA Mutation | p.Ala165Val(p.A165V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101182860:101182860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1108A>G |
| AA Mutation | p.Lys370Glu(p.K370E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101209676:101209676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Ala58Val(p.A58V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101209701:101209701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.148C>T |
| AA Mutation | p.Arg50Cys(p.R50C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536262 |
| Start | 101209700:101209700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.149G>A |
| AA Mutation | p.Arg50His(p.R50H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000536262 |
| Start | 101187452:101187452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147034851 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000536262 |
| Start | 101209645:101209645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000536262 |
| Start | 101209738:101209738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141426258 |
| CDS Mutation | c.111C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000536262 |
| Start | 101195140:101195140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143104107 |
| CDS Mutation | c.492C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |