Primary Site >> Stomach Cancer
Gene >> IQGAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90441649:90441649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.793G>A |
| AA Mutation | p.Ala265Thr(p.A265T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90474098:90474098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2540G>A |
| AA Mutation | p.Arg847Gln(p.R847Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90494724:90494724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4640A>G |
| AA Mutation | p.Lys1547Arg(p.K1547R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90491391:90491391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4307A>C |
| AA Mutation | p.Asp1436Ala(p.D1436A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90494732:90494732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4648G>A |
| AA Mutation | p.Glu1550Lys(p.E1550K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90476770:90476770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2892G>C |
| AA Mutation | p.Glu964Asp(p.E964D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90433762:90433762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.434T>C |
| AA Mutation | p.Met145Thr(p.M145T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90466423:90466423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2022A>C |
| AA Mutation | p.Lys674Asn(p.K674N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90452823:90452823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1211C>T |
| AA Mutation | p.Ala404Val(p.A404V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90473956:90473956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2494T>G |
| AA Mutation | p.Phe832Val(p.F832V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90466302:90466302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1901T>C |
| AA Mutation | p.Val634Ala(p.V634A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90492609:90492609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4526C>T |
| AA Mutation | p.Thr1509Ile(p.T1509I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90454523:90454523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1583T>G |
| AA Mutation | p.Val528Gly(p.V528G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90441557:90441557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701C>T |
| AA Mutation | p.Ala234Val(p.A234V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000268182 |
| Start | 90484221:90484221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763205486 |
| CDS Mutation | c.3790C>T |
| AA Mutation | p.Arg1264Trp(p.R1264W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268182 |
| Start | 90492613:90492613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4530C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268182 |
| Start | 90484340:90484340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268182 |
| Start | 90453251:90453251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1446A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268182 |
| Start | 90429657:90429657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.381A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268182 |
| Start | 90476693:90476693(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771739474 |
| CDS Mutation | c.2822delA |
| AA Mutation | p.Asn941IlefsTer8(p.N941Ifs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |