Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.86510853C>A | CA397005838 | FOXF1 | c.284C>A (p.Ser95Tyr) | |
16 | g.86510853C>G | CA397005840 | FOXF1 | c.284C>G (p.Ser95Cys) | |
16 | g.86510853C>T | CA397005842 | FOXF1 | c.284C>T (p.Ser95Phe) | |
16 | g.86510854C>A | CA497013752 | FOXF1 | c.285C>A (p.Ser95=) | |
16 | g.86510854C= | CA2239913469 | FOXF1 | c.285C= (p.Ser95=) | |
16 | g.86510854C>G | CA497013753 | FOXF1 | c.285C>G (p.Ser95=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.86510854C>T | CA497013754 | FOXF1 | c.285C>T (p.Ser95=) | |
16 | g.86510855G>A | CA397005846 | FOXF1 | c.286G>A (p.Val96Met) | |
16 | g.86510855G>C | CA397005844 | FOXF1 | c.286G>C (p.Val96Leu) | |
16 | g.86510855G= | CA2239913470 | FOXF1 | c.286G= (p.Val96=) | |
16 | g.86510855G>T | CA397005843 | FOXF1 | c.286G>T (p.Val96Leu) | ClinVar dbSNP |
16 | g.86510856T>A | CA397005849 | FOXF1 | c.287T>A (p.Val96Glu) | |
16 | g.86510856T>C | CA397005850 | FOXF1 | c.287T>C (p.Val96Ala) | |
16 | g.86510856T>G | CA397005852 | FOXF1 | c.287T>G (p.Val96Gly) | |
16 | g.86510857G>A | CA497013763 | FOXF1 | c.288G>A (p.Val96=) | gnomAD v4 |
16 | g.86510857G>C | CA497013764 | FOXF1 | c.288G>C (p.Val96=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.86510857G= | CA2239913471 | FOXF1 | c.288G= (p.Val96=) | |
16 | g.86510857G>T | CA497013765 | FOXF1 | c.288G>T (p.Val96=) | |
16 | g.86510858C>A | CA397005854 | FOXF1 | c.289C>A (p.Arg97Ser) | |
16 | g.86510858C>G | CA397005856 | FOXF1 | c.289C>G (p.Arg97Gly) | |
16 | g.86510858C>T | CA397005857 | FOXF1 | c.289C>T (p.Arg97Cys) | |
16 | g.86510859G>A | CA397005860 | FOXF1 | c.290G>A (p.Arg97His) | gnomAD v4 |
16 | g.86510859G>C | CA397005862 | FOXF1 | c.290G>C (p.Arg97Pro) | |
16 | g.86510859G>T | CA397005864 | FOXF1 | c.290G>T (p.Arg97Leu) | |
16 | g.86510860C>A | CA497013771 | FOXF1 | c.291C>A (p.Arg97=) | COSMIC COSMIC |
16 | g.86510860C= | CA2239913472 | FOXF1 | c.291C= (p.Arg97=) | |
16 | g.86510860C>G | CA497013773 | FOXF1 | c.291C>G (p.Arg97=) | |
16 | g.86510860C>T | CA497013776 | FOXF1 | c.291C>T (p.Arg97=) | |
16 | g.86510861C>A | CA397005867 | FOXF1 | c.292C>A (p.His98Asn) | |
16 | g.86510861C>G | CA397005868 | FOXF1 | c.292C>G (p.His98Asp) | |
16 | g.86510861C>T | CA397005870 | FOXF1 | c.292C>T (p.His98Tyr) | |
16 | g.86510863_86510864dup | CA8217376 | FOXF1 | c.294_295dup (p.Asn99ThrfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.86510862A>C | CA397005871 | FOXF1 | c.293A>C (p.His98Pro) | |
16 | g.86510862A>G | CA397005874 | FOXF1 | c.293A>G (p.His98Arg) | |
16 | g.86510862A>T | CA397005872 | FOXF1 | c.293A>T (p.His98Leu) | |
16 | g.86510863C>A | CA397005876 | FOXF1 | c.294C>A (p.His98Gln) | ClinVar dbSNP |
16 | g.86510863C= | CA2239913473 | FOXF1 | c.294C= (p.His98=) | |
16 | g.86510863C>G | CA397005878 | FOXF1 | c.294C>G (p.His98Gln) | |
16 | g.86510863C>T | CA497013787 | FOXF1 | c.294C>T (p.His98=) | |
16 | g.86510864A>C | CA397005879 | FOXF1 | c.295A>C (p.Asn99His) | |
16 | g.86510864A>G | CA397005881 | FOXF1 | c.295A>G (p.Asn99Asp) | |
16 | g.86510864A>T | CA397005883 | FOXF1 | c.295A>T (p.Asn99Tyr) | |
16 | g.86510865A>C | CA397005885 | FOXF1 | c.296A>C (p.Asn99Thr) | |
16 | g.86510865A>G | CA397005887 | FOXF1 | c.296A>G (p.Asn99Ser) | |
16 | g.86510865A>T | CA397005888 | FOXF1 | c.296A>T (p.Asn99Ile) | |
16 | g.86510866C>A | CA397005889 | FOXF1 | c.297C>A (p.Asn99Lys) | |
16 | g.86510866C= | CA2239913474 | FOXF1 | c.297C= (p.Asn99=) | |
16 | g.86510866C>G | CA397005890 | FOXF1 | c.297C>G (p.Asn99Lys) | |
16 | g.86510866C>T | CA497013799 | FOXF1 | c.297C>T (p.Asn99=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.86510867C>A | CA397005897 | FOXF1 | c.298C>A (p.Leu100Ile) |