Primary Site >> Stomach Cancer
Gene >> DHX8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492907:43492907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199963654 |
| CDS Mutation | c.730C>T |
| AA Mutation | p.Arg244Trp(p.R244W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492926:43492926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746384849 |
| CDS Mutation | c.749G>A |
| AA Mutation | p.Arg250Gln(p.R250Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262415 |
| Start | 43507687:43507687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2108A>G |
| AA Mutation | p.Lys703Arg(p.K703R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43507159:43507159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1885A>G |
| AA Mutation | p.Arg629Gly(p.R629G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43493836:43493836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763218908 |
| CDS Mutation | c.1162C>T |
| AA Mutation | p.Arg388Cys(p.R388C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43507821:43507821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764176155 |
| CDS Mutation | c.2122C>T |
| AA Mutation | p.Arg708Trp(p.R708W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43523749:43523749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3565C>G |
| AA Mutation | p.Leu1189Val(p.L1189V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43491180:43491180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.323C>A |
| AA Mutation | p.Pro108His(p.P108H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43504733:43504733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1636A>G |
| AA Mutation | p.Asn546Asp(p.N546D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43521444:43521444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3142G>A |
| AA Mutation | p.Val1048Met(p.V1048M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492890:43492890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713G>A |
| AA Mutation | p.Arg238Gln(p.R238Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492944:43492944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749482546 |
| CDS Mutation | c.767G>A |
| AA Mutation | p.Arg256His(p.R256H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492889:43492889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712C>T |
| AA Mutation | p.Arg238Trp(p.R238W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43520865:43520865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3052T>G |
| AA Mutation | p.Phe1018Val(p.F1018V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262415 |
| Start | 43492881:43492881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763284184 |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Arg235Gln(p.R235Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |