Primary Site >> Stomach Cancer
Gene >> HRH4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477107:24477107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.718G>A |
| AA Mutation | p.Ala240Thr(p.A240T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24476906:24476906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517T>C |
| AA Mutation | p.Tyr173His(p.Y173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477374:24477374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.985T>C |
| AA Mutation | p.Tyr329His(p.Y329H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477546:24477546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150959048 |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Arg386Gln(p.R386Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477138:24477138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.749C>T |
| AA Mutation | p.Ser250Leu(p.S250L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477551:24477551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1162G>T |
| AA Mutation | p.Val388Leu(p.V388L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24476997:24476997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.608A>C |
| AA Mutation | p.Lys203Thr(p.K203T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256906 |
| Start | 24460864:24460864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136C>T |
| AA Mutation | p.Leu46Phe(p.L46F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256906 |
| Start | 24468822:24468822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758519592 |
| CDS Mutation | c.228G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256906 |
| Start | 24477514:24477514(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1130delA |
| AA Mutation | p.Lys377SerfsTer30(p.K377Sfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |