Primary Site >> Stomach Cancer
Gene >> POU5F1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416423:127416423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.557G>A |
| AA Mutation | p.Arg186His(p.R186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416087:127416087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773140691 |
| CDS Mutation | c.221C>T |
| AA Mutation | p.Ala74Val(p.A74V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416618:127416618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.752A>G |
| AA Mutation | p.Gln251Arg(p.Q251R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416162:127416162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.296C>G |
| AA Mutation | p.Ala99Gly(p.A99G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416911:127416911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1045G>A |
| AA Mutation | p.Val349Ile(p.V349I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416202:127416202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747198568 |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416652:127416652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416169:127416169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000465342 |
| Start | 127416217:127416217(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs763078225 |
| CDS Mutation | c.356delC |
| AA Mutation | p.Pro119LeufsTer4(p.P119Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |