Primary Site >> Stomach Cancer
Gene >> B4GALNT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49160627:49160627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.932A>G |
| AA Mutation | p.Tyr311Cys(p.Y311C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49159116:49159116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.758A>C |
| AA Mutation | p.Lys253Thr(p.K253T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49160582:49160582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.887C>T |
| AA Mutation | p.Ala296Val(p.A296V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49166168:49166168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1189C>A |
| AA Mutation | p.Leu397Ile(p.L397I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49152831:49152831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375362269 |
| CDS Mutation | c.565G>A |
| AA Mutation | p.Val189Ile(p.V189I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49133140:49133140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115G>A |
| AA Mutation | p.Gly39Arg(p.G39R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49169723:49169723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199908433 |
| CDS Mutation | c.1696G>A |
| AA Mutation | p.Ala566Thr(p.A566T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300404 |
| Start | 49164135:49164135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145043273 |
| CDS Mutation | c.994C>T |
| AA Mutation | p.Arg332Cys(p.R332C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300404 |
| Start | 49159189:49159189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114986987 |
| CDS Mutation | c.831G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300404 |
| Start | 49142128:49142128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300404 |
| Start | 49156594:49156594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376911707 |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |