Primary Site >> Stomach Cancer
Gene >> RASAL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261729 |
| Start | 113116020:113116020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531834126 |
| CDS Mutation | c.763C>T |
| AA Mutation | p.Arg255Cys(p.R255C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261729 |
| Start | 113128155:113128155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.146T>A |
| AA Mutation | p.Leu49Gln(p.L49Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261729 |
| Start | 113105802:113105802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1739C>T |
| AA Mutation | p.Ala580Val(p.A580V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261729 |
| Start | 113119211:113119211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375528107 |
| CDS Mutation | c.559C>T |
| AA Mutation | p.Arg187Trp(p.R187W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261729 |
| Start | 113115685:113115685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.953T>C |
| AA Mutation | p.Leu318Pro(p.L318P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261729 |
| Start | 113105849:113105849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368835731 |
| CDS Mutation | c.1692G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261729 |
| Start | 113105789:113105789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139573405 |
| CDS Mutation | c.1752G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261729 |
| Start | 113104188:113104188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1938G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261729 |
| Start | 113104266:113104266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261729 |
| Start | 113116048:113116048(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.735delG |
| AA Mutation | p.Asn246ThrfsTer7(p.N246Tfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261729 |
| Start | 113101968:113101968(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2143delG |
| AA Mutation | p.Asp715ThrfsTer28(p.D715Tfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261729 |
| Start | 113116032:113116032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763097544 |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Arg251Ter(p.R251*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |