Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.108561702T>ACA365338642FOXO3c.494T>A (p.Leu165Gln)
6g.108561702T>CCA365338643FOXO3c.494T>C (p.Leu165Pro)
6g.108561702T>GCA365338644FOXO3c.494T>G (p.Leu165Arg)
6g.108561703G>ACA3949237FOXO3c.495G>A (p.Leu165=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.108561703G>CCA3949236FOXO3c.495G>C (p.Leu165=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.108561703G=CA1654338366FOXO3c.495G= (p.Leu165=)
6g.108561703G>TCA451920507FOXO3c.495G>T (p.Leu165=)
COSMIC
6g.108561704_108561779dupCA2679911224FOXO3c.496_571dup (p.Val191AspfsTer32)
gnomAD v4
6g.108561704A>CCA365338645FOXO3c.496A>C (p.Ile166Leu)
6g.108561704A>GCA365338647FOXO3c.496A>G (p.Ile166Val)
6g.108561704A>TCA365338646FOXO3c.496A>T (p.Ile166Phe)
6g.108561705T>ACA365338648FOXO3c.497T>A (p.Ile166Asn)
6g.108561705T>CCA365338649FOXO3c.497T>C (p.Ile166Thr)
6g.108561705T>GCA365338650FOXO3c.497T>G (p.Ile166Ser)
6g.108561706C>ACA451920513FOXO3c.498C>A (p.Ile166=)
dbSNP gnomAD v2 gnomAD v4
6g.108561706C=CA1654338370FOXO3c.498C= (p.Ile166=)
6g.108561706C>GCA365338651FOXO3c.498C>G (p.Ile166Met)
6g.108561706C>TCA451920512FOXO3c.498C>T (p.Ile166=)
6g.108561707A>CCA365338652FOXO3c.499A>C (p.Thr167Pro)
6g.108561707A>GCA365338653FOXO3c.499A>G (p.Thr167Ala)
6g.108561707A>TCA365338654FOXO3c.499A>T (p.Thr167Ser)
6g.108561708C>ACA365338655FOXO3c.500C>A (p.Thr167Asn)
6g.108561708C=CA1654338378FOXO3c.500C= (p.Thr167=)
6g.108561708C>GCA365338656FOXO3c.500C>G (p.Thr167Ser)
6g.108561708C>TCA365338657FOXO3c.500C>T (p.Thr167Ile)
dbSNP gnomAD v4
6g.108561709C>ACA451920517FOXO3c.501C>A (p.Thr167=)
6g.108561709C>GCA451920519FOXO3c.501C>G (p.Thr167=)
6g.108561709C>TCA451920518FOXO3c.501C>T (p.Thr167=)
6g.108561710C>ACA365338658FOXO3c.502C>A (p.Arg168Ser)
6g.108561710C>GCA365338659FOXO3c.502C>G (p.Arg168Gly)
gnomAD v4
6g.108561710C>TCA365338660FOXO3c.502C>T (p.Arg168Cys)
gnomAD v4
6g.108561711G>ACA3949238FOXO3c.503G>A (p.Arg168His)
dbSNP ExAC gnomAD v2 COSMIC
6g.108561711G>CCA365338661FOXO3c.503G>C (p.Arg168Pro)
6g.108561711G=CA1654338381FOXO3c.503G= (p.Arg168=)
6g.108561711G>TCA365338662FOXO3c.503G>T (p.Arg168Leu)
gnomAD v4
6g.108561712C>ACA451920521FOXO3c.504C>A (p.Arg168=)
6g.108561712C=CA1654338394FOXO3c.504C= (p.Arg168=)
6g.108561712C>GCA451920522FOXO3c.504C>G (p.Arg168=)
gnomAD v4
6g.108561712C>TCA3949239FOXO3c.504C>T (p.Arg168=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.108561713G>ACA365338663FOXO3c.505G>A (p.Ala169Thr)
6g.108561713G>CCA365338664FOXO3c.505G>C (p.Ala169Pro)
6g.108561713G>TCA365338665FOXO3c.505G>T (p.Ala169Ser)
6g.108561714C>ACA365338666FOXO3c.506C>A (p.Ala169Asp)
6g.108561714C=CA1654338399FOXO3c.506C= (p.Ala169=)
6g.108561714C>GCA365338667FOXO3c.506C>G (p.Ala169Gly)
6g.108561714C>TCA365338668FOXO3c.506C>T (p.Ala169Val)
dbSNP gnomAD v2
6g.108561715C>ACA451920527FOXO3c.507C>A (p.Ala169=)
gnomAD v4
6g.108561715C=CA1654338403FOXO3c.507C= (p.Ala169=)
6g.108561715C>GCA451920528FOXO3c.507C>G (p.Ala169=)
6g.108561715C>TCA3949240FOXO3c.507C>T (p.Ala169=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched