Primary Site >> Stomach Cancer
Gene >> HOXD13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094708:176094708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753726144 |
| CDS Mutation | c.1010A>G |
| AA Mutation | p.Lys337Arg(p.K337R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094488:176094488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373737493 |
| CDS Mutation | c.790G>T |
| AA Mutation | p.Ala264Ser(p.A264S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094609:176094609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376366804 |
| CDS Mutation | c.911A>G |
| AA Mutation | p.Asp304Gly(p.D304G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093546:176093546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.656G>A |
| AA Mutation | p.Arg219Gln(p.R219Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094649:176094649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.951G>T |
| AA Mutation | p.Glu317Asp(p.E317D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093339:176093339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Ala150Val(p.A150V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093617:176093617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.727T>C |
| AA Mutation | p.Tyr243His(p.Y243H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093151:176093151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.261G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093493:176093493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.603G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094487:176094487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392539 |
| Start | 176093427:176093427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.537G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392539 |
| Start | 176094511:176094511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199982017 |
| CDS Mutation | c.813C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |