Primary Site >> Stomach Cancer
Gene >> SELP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169603056:169603056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144811959 |
| CDS Mutation | c.1675C>T |
| AA Mutation | p.Arg559Cys(p.R559C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169611611:169611611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764864800 |
| CDS Mutation | c.1028C>A |
| AA Mutation | p.Ala343Asp(p.A343D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169617268:169617268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.241A>G |
| AA Mutation | p.Lys81Glu(p.K81E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169595971:169595971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2055C>G |
| AA Mutation | p.Ser685Arg(p.S685R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169591444:169591444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2420G>T |
| AA Mutation | p.Cys807Phe(p.C807F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169594773:169594773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2206G>C |
| AA Mutation | p.Glu736Gln(p.E736Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263686 |
| Start | 169613033:169613033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767813249 |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Ser224Leu(p.S224L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263686 |
| Start | 169612275:169612275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753970351 |
| CDS Mutation | c.903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |