Primary Site >> Stomach Cancer
Gene >> HOXD10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176117491:176117491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779016325 |
| CDS Mutation | c.658G>A |
| AA Mutation | p.Glu220Lys(p.E220K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176116966:176116966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.133A>G |
| AA Mutation | p.Thr45Ala(p.T45A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176119044:176119044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.836T>C |
| AA Mutation | p.Leu279Pro(p.L279P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176119115:176119115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373028650 |
| CDS Mutation | c.907G>A |
| AA Mutation | p.Val303Ile(p.V303I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176117257:176117257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Glu142Lys(p.E142K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249501 |
| Start | 176116862:176116862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.29C>A |
| AA Mutation | p.Ala10Asp(p.A10D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249501 |
| Start | 176117418:176117418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249501 |
| Start | 176119228:176119228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1020T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249501 |
| Start | 176117313:176117313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249501 |
| Start | 176116998:176116998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.165G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249501 |
| Start | 176117385:176117385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756832722 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |