Primary Site >> Stomach Cancer
Gene >> ALPP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381290:232381290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760691687 |
| CDS Mutation | c.1232C>T |
| AA Mutation | p.Thr411Met(p.T411M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379881:232379881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371349871 |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Arg201His(p.R201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381578:232381578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391G>A |
| AA Mutation | p.Arg464His(p.R464H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379221:232379221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Thr72Ile(p.T72I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232380712:232380712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753036535 |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Arg319Cys(p.R319C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381361:232381361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146681711 |
| CDS Mutation | c.1303G>A |
| AA Mutation | p.Glu435Lys(p.E435K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379865:232379865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148017705 |
| CDS Mutation | c.586G>A |
| AA Mutation | p.Val196Met(p.V196M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379084:232379084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.190G>C |
| AA Mutation | p.Asp64His(p.D64H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379215:232379215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766177947 |
| CDS Mutation | c.209C>T |
| AA Mutation | p.Thr70Met(p.T70M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392027 |
| Start | 232378821:232378821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19C>G |
| AA Mutation | p.Leu7Val(p.L7V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381309:232381309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1251C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381336:232381336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1278C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381537:232381537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140739243 |
| CDS Mutation | c.1350C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379777:232379777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381504:232381504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1317C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232379843:232379843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381555:232381555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232380708:232380708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392027 |
| Start | 232381360:232381360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751295066 |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |