Primary Site >> Stomach Cancer
Gene >> HTRA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122514217:122514217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1301T>C |
| AA Mutation | p.Ile434Thr(p.I434T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122489529:122489529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754158219 |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227Gln(p.R227Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122506874:122506874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587776449 |
| CDS Mutation | c.961G>A |
| AA Mutation | p.Ala321Thr(p.A321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122512053:122512053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1262C>T |
| AA Mutation | p.Thr421Ile(p.T421I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122489495:122489495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761429963 |
| CDS Mutation | c.646G>A |
| AA Mutation | p.Val216Met(p.V216M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122489603:122489603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113993968 |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Ala252Thr(p.A252T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122489552:122489552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.703G>A |
| AA Mutation | p.Gly235Ser(p.G235S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122506818:122506818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905G>A |
| AA Mutation | p.Arg302Gln(p.R302Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368984 |
| Start | 122508764:122508764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1114G>A |
| AA Mutation | p.Ala372Thr(p.A372T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368984 |
| Start | 122506768:122506768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138702840 |
| CDS Mutation | c.855G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368984 |
| Start | 122514266:122514266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374675648 |
| CDS Mutation | c.1350C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |