Primary Site >> Stomach Cancer
Gene >> RANGAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41264822:41264822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143626610 |
| CDS Mutation | c.322A>G |
| AA Mutation | p.Ile108Val(p.I108V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41256102:41256102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.992A>G |
| AA Mutation | p.Asn331Ser(p.N331S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41261528:41261528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533A>G |
| AA Mutation | p.Lys178Arg(p.K178R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41256060:41256060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1034T>C |
| AA Mutation | p.Leu345Pro(p.L345P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41258060:41258060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144343100 |
| CDS Mutation | c.662A>G |
| AA Mutation | p.Asn221Ser(p.N221S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41274682:41274682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158C>T |
| AA Mutation | p.Ala53Val(p.A53V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41252909:41252909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1343G>A |
| AA Mutation | p.Arg448His(p.R448H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356244 |
| Start | 41280989:41280989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.56C>T |
| AA Mutation | p.Ala19Val(p.A19V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41256732:41256732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531001209 |
| CDS Mutation | c.867C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41254386:41254386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41264670:41264670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773090708 |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41261473:41261473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200548054 |
| CDS Mutation | c.588C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41254398:41254398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41280979:41280979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356244 |
| Start | 41254401:41254401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776143659 |
| CDS Mutation | c.1167A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |