Primary Site >> Stomach Cancer
Gene >> ARMCX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553802:101553802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.872T>C |
| AA Mutation | p.Val291Ala(p.V291A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553504:101553504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.574T>G |
| AA Mutation | p.Phe192Val(p.F192V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553114:101553114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.184G>A |
| AA Mutation | p.Ala62Thr(p.A62T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553161:101553161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.231G>T |
| AA Mutation | p.Lys77Asn(p.K77N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372829 |
| Start | 101554076:101554076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1146T>G |
| AA Mutation | p.Asp382Glu(p.D382E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553272:101553272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.342G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372829 |
| Start | 101553053:101553053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150448743 |
| CDS Mutation | c.123C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |