Primary Site >> Stomach Cancer
Gene >> ARHGEF12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120448242:120448242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1631T>C |
| AA Mutation | p.Met544Thr(p.M544T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120447060:120447060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1564A>T |
| AA Mutation | p.Ile522Phe(p.I522F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120421842:120421842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767889107 |
| CDS Mutation | c.338G>A |
| AA Mutation | p.Arg113Gln(p.R113Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120480288:120480288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4095G>A |
| AA Mutation | p.Met1365Ile(p.M1365I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120449197:120449197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577733342 |
| CDS Mutation | c.1826G>A |
| AA Mutation | p.Arg609His(p.R609H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120478196:120478196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3573A>C |
| AA Mutation | p.Lys1191Asn(p.K1191N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120480133:120480133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3940C>T |
| AA Mutation | p.Pro1314Ser(p.P1314S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120451541:120451541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754173692 |
| CDS Mutation | c.1873C>T |
| AA Mutation | p.Arg625Cys(p.R625C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120467218:120467218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2764C>A |
| AA Mutation | p.Arg922Ser(p.R922S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120480179:120480179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3986G>A |
| AA Mutation | p.Arg1329Gln(p.R1329Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120460741:120460741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2597A>T |
| AA Mutation | p.Glu866Val(p.E866V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120480346:120480346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750431916 |
| CDS Mutation | c.4153C>T |
| AA Mutation | p.Arg1385Cys(p.R1385C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120428101:120428101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779478124 |
| CDS Mutation | c.439C>T |
| AA Mutation | p.Arg147Cys(p.R147C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397843 |
| Start | 120446442:120446442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189894068 |
| CDS Mutation | c.1385G>A |
| AA Mutation | p.Arg462His(p.R462H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397843 |
| Start | 120481411:120481411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4389C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397843 |
| Start | 120465242:120465242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772799606 |
| CDS Mutation | c.2619C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |