Primary Site >> Stomach Cancer
Gene >> GFRA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116270854:116270854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.302G>A |
| AA Mutation | p.Arg101His(p.R101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116096724:116096724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811T>C |
| AA Mutation | p.Ser271Pro(p.S271P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116125326:116125326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665C>A |
| AA Mutation | p.Thr222Lys(p.T222K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116089890:116089890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757403878 |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Asp350Asn(p.D350N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116093794:116093794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761924829 |
| CDS Mutation | c.923G>T |
| AA Mutation | p.Ser308Ile(p.S308I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116125422:116125422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376230694 |
| CDS Mutation | c.569G>A |
| AA Mutation | p.Arg190His(p.R190H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116270949:116270949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207G>T |
| AA Mutation | p.Lys69Asn(p.K69N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355422 |
| Start | 116125461:116125461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530C>A |
| AA Mutation | p.Pro177Gln(p.P177Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355422 |
| Start | 116270904:116270904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355422 |
| Start | 116089861:116089861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1077A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355422 |
| Start | 116271090:116271090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.66C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355422 |
| Start | 116125475:116125475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371921058 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355422 |
| Start | 116096752:116096752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149392755 |
| CDS Mutation | c.783G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355422 |
| Start | 116089763:116089763(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1175delT |
| AA Mutation | p.Leu392CysfsTer12(p.L392Cfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |