Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.86510853C>ACA397005838FOXF1c.284C>A (p.Ser95Tyr)
16g.86510853C>GCA397005840FOXF1c.284C>G (p.Ser95Cys)
16g.86510853C>TCA397005842FOXF1c.284C>T (p.Ser95Phe)
16g.86510854C>ACA497013752FOXF1c.285C>A (p.Ser95=)
16g.86510854C=CA2239913469FOXF1c.285C= (p.Ser95=)
16g.86510854C>GCA497013753FOXF1c.285C>G (p.Ser95=)
dbSNP gnomAD v2 gnomAD v4
16g.86510854C>TCA497013754FOXF1c.285C>T (p.Ser95=)
16g.86510855G>ACA397005846FOXF1c.286G>A (p.Val96Met)
16g.86510855G>CCA397005844FOXF1c.286G>C (p.Val96Leu)
16g.86510855G=CA2239913470FOXF1c.286G= (p.Val96=)
16g.86510855G>TCA397005843FOXF1c.286G>T (p.Val96Leu)
ClinVar dbSNP
16g.86510856T>ACA397005849FOXF1c.287T>A (p.Val96Glu)
16g.86510856T>CCA397005850FOXF1c.287T>C (p.Val96Ala)
16g.86510856T>GCA397005852FOXF1c.287T>G (p.Val96Gly)
16g.86510857G>ACA497013763FOXF1c.288G>A (p.Val96=)
gnomAD v4
16g.86510857G>CCA497013764FOXF1c.288G>C (p.Val96=)
dbSNP gnomAD v2 gnomAD v4
16g.86510857G=CA2239913471FOXF1c.288G= (p.Val96=)
16g.86510857G>TCA497013765FOXF1c.288G>T (p.Val96=)
16g.86510858C>ACA397005854FOXF1c.289C>A (p.Arg97Ser)
16g.86510858C>GCA397005856FOXF1c.289C>G (p.Arg97Gly)
16g.86510858C>TCA397005857FOXF1c.289C>T (p.Arg97Cys)
16g.86510859G>ACA397005860FOXF1c.290G>A (p.Arg97His)
gnomAD v4
16g.86510859G>CCA397005862FOXF1c.290G>C (p.Arg97Pro)
16g.86510859G>TCA397005864FOXF1c.290G>T (p.Arg97Leu)
16g.86510860C>ACA497013771FOXF1c.291C>A (p.Arg97=)
COSMIC COSMIC
16g.86510860C=CA2239913472FOXF1c.291C= (p.Arg97=)
16g.86510860C>GCA497013773FOXF1c.291C>G (p.Arg97=)
16g.86510860C>TCA497013776FOXF1c.291C>T (p.Arg97=)
16g.86510861C>ACA397005867FOXF1c.292C>A (p.His98Asn)
16g.86510861C>GCA397005868FOXF1c.292C>G (p.His98Asp)
16g.86510861C>TCA397005870FOXF1c.292C>T (p.His98Tyr)
16g.86510863_86510864dupCA8217376FOXF1c.294_295dup (p.Asn99ThrfsTer?)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.86510862A>CCA397005871FOXF1c.293A>C (p.His98Pro)
16g.86510862A>GCA397005874FOXF1c.293A>G (p.His98Arg)
16g.86510862A>TCA397005872FOXF1c.293A>T (p.His98Leu)
16g.86510863C>ACA397005876FOXF1c.294C>A (p.His98Gln)
ClinVar dbSNP
16g.86510863C=CA2239913473FOXF1c.294C= (p.His98=)
16g.86510863C>GCA397005878FOXF1c.294C>G (p.His98Gln)
16g.86510863C>TCA497013787FOXF1c.294C>T (p.His98=)
16g.86510864A>CCA397005879FOXF1c.295A>C (p.Asn99His)
16g.86510864A>GCA397005881FOXF1c.295A>G (p.Asn99Asp)
16g.86510864A>TCA397005883FOXF1c.295A>T (p.Asn99Tyr)
16g.86510865A>CCA397005885FOXF1c.296A>C (p.Asn99Thr)
16g.86510865A>GCA397005887FOXF1c.296A>G (p.Asn99Ser)
16g.86510865A>TCA397005888FOXF1c.296A>T (p.Asn99Ile)
16g.86510866C>ACA397005889FOXF1c.297C>A (p.Asn99Lys)
16g.86510866C=CA2239913474FOXF1c.297C= (p.Asn99=)
16g.86510866C>GCA397005890FOXF1c.297C>G (p.Asn99Lys)
16g.86510866C>TCA497013799FOXF1c.297C>T (p.Asn99=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.86510867C>ACA397005897FOXF1c.298C>A (p.Leu100Ile)

Number of alleles fetched