Primary Site >> Stomach Cancer
Gene >> CCAR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68747452:68747452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.712G>T |
| AA Mutation | p.Val238Phe(p.V238F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68753911:68753911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1178A>G |
| AA Mutation | p.Asp393Gly(p.D393G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68771225:68771225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2318T>C |
| AA Mutation | p.Leu773Pro(p.L773P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68747253:68747253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611G>A |
| AA Mutation | p.Arg204Lys(p.R204K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265872 |
| Start | 68749684:68749684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1117T>C |
| AA Mutation | p.Cys373Arg(p.C373R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68766041:68766041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2260G>A |
| AA Mutation | p.Asp754Asn(p.D754N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68791234:68791234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201223388 |
| CDS Mutation | c.3421C>A |
| AA Mutation | p.Gln1141Lys(p.Q1141K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68789746:68789746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3224C>T |
| AA Mutation | p.Ser1075Phe(p.S1075F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68749646:68749646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1079C>T |
| AA Mutation | p.Pro360Leu(p.P360L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265872 |
| Start | 68753881:68753881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779871042 |
| CDS Mutation | c.1148G>A |
| AA Mutation | p.Arg383His(p.R383H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265872 |
| Start | 68756441:68756441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1794C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265872 |
| Start | 68765962:68765962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149316365 |
| CDS Mutation | c.2181G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |