Primary Site >> Stomach Cancer
Gene >> ARHGEF5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000056217 |
| Start | 144363890:144363890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1221G>A |
| AA Mutation | p.Met407Ile(p.M407I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000056217 |
| Start | 144366411:144366411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769037711 |
| CDS Mutation | c.3211C>T |
| AA Mutation | p.Arg1071Trp(p.R1071W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000056217 |
| Start | 144373238:144373238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4094C>T |
| AA Mutation | p.Thr1365Ile(p.T1365I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000056217 |
| Start | 144371222:144371222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3593A>G |
| AA Mutation | p.Asp1198Gly(p.D1198G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000056217 |
| Start | 144378823:144378823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4593G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000056217 |
| Start | 144363590:144363590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.921G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000056217 |
| Start | 144380032:144380032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4770A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000056217 |
| Start | 144378835:144378835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186937905 |
| CDS Mutation | c.4605C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000056217 |
| Start | 144378765:144378765(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4540delC |
| AA Mutation | p.Gln1514ArgfsTer24(p.Q1514Rfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000056217 |
| Start | 144363398:144363399(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.729_730insTAATATCT |
| AA Mutation | p.Gly244Ter(p.G244*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000056217 |
| Start | 144371305:144371305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761806185 |
| CDS Mutation | c.3676C>T |
| AA Mutation | p.Arg1226Ter(p.R1226*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000056217 |
| Start | 144363375:144363375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Gln236Ter(p.Q236*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |