Primary Site >> Stomach Cancer
Gene >> HYOU1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119055267:119055267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.337G>A |
| AA Mutation | p.Val113Ile(p.V113I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119052726:119052726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782034654 |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Arg300Trp(p.R300W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119054588:119054588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.584C>T |
| AA Mutation | p.Ala195Val(p.A195V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119049833:119049833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1670A>C |
| AA Mutation | p.Glu557Ala(p.E557A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119048795:119048795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2084T>C |
| AA Mutation | p.Met695Thr(p.M695T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119051579:119051579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1385T>C |
| AA Mutation | p.Leu462Pro(p.L462P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119045619:119045619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2974C>T |
| AA Mutation | p.Arg992Trp(p.R992W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119052097:119052097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781881422 |
| CDS Mutation | c.1198G>A |
| AA Mutation | p.Val400Met(p.V400M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119055248:119055248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781974767 |
| CDS Mutation | c.356G>A |
| AA Mutation | p.Arg119His(p.R119H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119049118:119049118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1892A>C |
| AA Mutation | p.Glu631Ala(p.E631A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119054550:119054550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.622G>A |
| AA Mutation | p.Ala208Thr(p.A208T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617285 |
| Start | 119054655:119054655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Val173Met(p.V173M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617285 |
| Start | 119048812:119048812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782680299 |
| CDS Mutation | c.2067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617285 |
| Start | 119051053:119051053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201408509 |
| CDS Mutation | c.1647C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |