Primary Site >> Stomach Cancer
Gene >> B4GALT5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371711 |
| Start | 49639769:49639769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.826A>C |
| AA Mutation | p.Ser276Arg(p.S276R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371711 |
| Start | 49640544:49640544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752406119 |
| CDS Mutation | c.728G>A |
| AA Mutation | p.Arg243His(p.R243H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371711 |
| Start | 49646973:49646973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.356C>T |
| AA Mutation | p.Pro119Leu(p.P119L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371711 |
| Start | 49640643:49640643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.629G>A |
| AA Mutation | p.Arg210Gln(p.R210Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371711 |
| Start | 49639705:49639705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.890G>A |
| AA Mutation | p.Gly297Asp(p.G297D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371711 |
| Start | 49636378:49636378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529151995 |
| CDS Mutation | c.1101C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |