Primary Site >> Stomach Cancer
Gene >> AHRR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 434154:434154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770662390 |
| CDS Mutation | c.1426G>A |
| AA Mutation | p.Gly476Ser(p.G476S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 423910:423910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Ser218Leu(p.S218L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 376688:376688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335C>T |
| AA Mutation | p.Ala112Val(p.A112V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 427859:427859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373499533 |
| CDS Mutation | c.773C>T |
| AA Mutation | p.Ala258Val(p.A258V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 432467:432467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925A>C |
| AA Mutation | p.Lys309Gln(p.K309Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000505113 |
| Start | 353812:353812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.157A>G |
| AA Mutation | p.Ser53Gly(p.S53G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 434507:434507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370473413 |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 433979:433979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1251G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 423896:423896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368710493 |
| CDS Mutation | c.639G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 433952:433952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369490421 |
| CDS Mutation | c.1224G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 353745:353745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761587153 |
| CDS Mutation | c.90G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 434477:434477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1749G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000505113 |
| Start | 433868:433868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1140G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000505113 |
| Start | 353729:353729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111551936 |
| CDS Mutation | c.75-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |