Primary Site >> Stomach Cancer
Gene >> FPR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51768882:51768882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144552448 |
| CDS Mutation | c.224C>T |
| AA Mutation | p.Thr75Met(p.T75M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51768968:51768968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199862216 |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Val104Met(p.V104M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51768735:51768735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778561198 |
| CDS Mutation | c.77G>A |
| AA Mutation | p.Arg26Gln(p.R26Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51769371:51769371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199892175 |
| CDS Mutation | c.713G>A |
| AA Mutation | p.Arg238His(p.R238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51769108:51769108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.450G>T |
| AA Mutation | p.Trp150Cys(p.W150C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51769205:51769205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.547T>C |
| AA Mutation | p.Trp183Arg(p.W183R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51768828:51768828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750225501 |
| CDS Mutation | c.170G>A |
| AA Mutation | p.Arg57His(p.R57H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51768765:51768765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.107C>A |
| AA Mutation | p.Thr36Asn(p.T36N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51769067:51769067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763580618 |
| CDS Mutation | c.409C>T |
| AA Mutation | p.Arg137Cys(p.R137C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340023 |
| Start | 51769379:51769379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772024580 |
| CDS Mutation | c.721C>T |
| AA Mutation | p.Arg241Trp(p.R241W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |