Primary Site >> Stomach Cancer
Gene >> RAPGEF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131584523:131584523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2749A>G |
| AA Mutation | p.Met917Val(p.M917V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131621898:131621898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1752G>T |
| AA Mutation | p.Lys584Asn(p.K584N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000372189 |
| Start | 131580263:131580263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764842655 |
| CDS Mutation | c.3083C>T |
| AA Mutation | p.Ala1028Val(p.A1028V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131621800:131621800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1850A>C |
| AA Mutation | p.Gln617Pro(p.Q617P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131589938:131589938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2257C>T |
| AA Mutation | p.Arg753Cys(p.R753C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131626167:131626167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201889315 |
| CDS Mutation | c.1406C>T |
| AA Mutation | p.Ala469Val(p.A469V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131626069:131626069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765844937 |
| CDS Mutation | c.1504G>A |
| AA Mutation | p.Val502Ile(p.V502I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131598254:131598254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2000A>C |
| AA Mutation | p.Glu667Ala(p.E667A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131580279:131580279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775152902 |
| CDS Mutation | c.3067C>T |
| AA Mutation | p.Arg1023Cys(p.R1023C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372189 |
| Start | 131626239:131626239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1334C>T |
| AA Mutation | p.Ala445Val(p.A445V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372189 |
| Start | 131596356:131596356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372772375 |
| CDS Mutation | c.2073C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372189 |
| Start | 131589921:131589921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376156893 |
| CDS Mutation | c.2274G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |