Primary Site >> Stomach Cancer
Gene >> HOXD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176152709:176152709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535C>G |
| AA Mutation | p.Leu179Val(p.L179V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176152650:176152650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751590168 |
| CDS Mutation | c.476C>T |
| AA Mutation | p.Thr159Met(p.T159M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176152761:176152761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754784160 |
| CDS Mutation | c.587G>A |
| AA Mutation | p.Arg196His(p.R196H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176152655:176152655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.481T>C |
| AA Mutation | p.Tyr161His(p.Y161H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176151684:176151684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.51C>A |
| AA Mutation | p.Phe17Leu(p.F17L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306324 |
| Start | 176151845:176151845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212C>T |
| AA Mutation | p.Ser71Leu(p.S71L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000306324 |
| Start | 176152064:176152064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765300039 |
| CDS Mutation | c.431C>T |
| AA Mutation | p.Ser144Leu(p.S144L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |