Primary Site >> Stomach Cancer
Gene >> ARHGAP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350060 |
| Start | 153919189:153919189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776A>G |
| AA Mutation | p.Asn259Ser(p.N259S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350060 |
| Start | 153910552:153910552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1876G>A |
| AA Mutation | p.Ala626Thr(p.A626T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350060 |
| Start | 153909801:153909801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782676556 |
| CDS Mutation | c.2354G>A |
| AA Mutation | p.Arg785Gln(p.R785Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153919027:153919027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.837C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153909466:153909466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2484C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153910365:153910365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1962C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153910191:153910191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141995493 |
| CDS Mutation | c.2136G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153907783:153907783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2787C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153910257:153910257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2070G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153910356:153910356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782818749 |
| CDS Mutation | c.1971C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350060 |
| Start | 153909514:153909514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61749033 |
| CDS Mutation | c.2436C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000350060 |
| Start | 153912727:153912728(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1514_1515delTT |
| AA Mutation | p.Phe505TrpfsTer34(p.F505Wfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |