Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.146340108delCA658820753POU4F3c.681del (p.Ile228SerfsTer14)
5g.146340108C>ACA447097909POU4F3c.681C>A (p.Thr227=)
5g.146340108C>GCA447097910POU4F3c.681C>G (p.Thr227=)
5g.146340108C>TCA447097912POU4F3c.681C>T (p.Thr227=)
gnomAD v4
5g.146340109A=CA1589086782POU4F3c.682A= (p.Ile228=)
5g.146340109A>CCA361621868POU4F3c.682A>C (p.Ile228Leu)
5g.146340109A>GCA361621870POU4F3c.682A>G (p.Ile228Val)
dbSNP gnomAD v4
5g.146340109A>TCA361621871POU4F3c.682A>T (p.Ile228Phe)
5g.146340110T>ACA361621875POU4F3c.683T>A (p.Ile228Asn)
5g.146340110T>CCA361621873POU4F3c.683T>C (p.Ile228Thr)
ClinVar dbSNP
5g.146340110T>GCA361621874POU4F3c.683T>G (p.Ile228Ser)
5g.146340110T=CA1589086783POU4F3c.683T= (p.Ile228=)
5g.146340111C>ACA447097916POU4F3c.684C>A (p.Ile228=)
5g.146340111C=CA1589086784POU4F3c.684C= (p.Ile228=)
5g.146340111C>GCA361621878POU4F3c.684C>G (p.Ile228Met)
5g.146340111C>TCA447097917POU4F3c.684C>T (p.Ile228=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.146340112T>ACA361621880POU4F3c.685T>A (p.Cys229Ser)
5g.146340112T>CCA361621882POU4F3c.685T>C (p.Cys229Arg)
5g.146340112T>GCA361621884POU4F3c.685T>G (p.Cys229Gly)
5g.146340113G>ACA361621885POU4F3c.686G>A (p.Cys229Tyr)
5g.146340113G>CCA361621886POU4F3c.686G>C (p.Cys229Ser)
5g.146340113G=CA1589086785POU4F3c.686G= (p.Cys229=)
5g.146340113G>TCA361621889POU4F3c.686G>T (p.Cys229Phe)
ClinVar dbSNP
5g.146340114C>ACA361621893POU4F3c.687C>A (p.Cys229Ter)
5g.146340114C>GCA361621895POU4F3c.687C>G (p.Cys229Trp)
5g.146340114C>TCA447097918POU4F3c.687C>T (p.Cys229=)
5g.146340115A>CCA447097920POU4F3c.688A>C (p.Arg230=)
5g.146340115A>GCA361621897POU4F3c.688A>G (p.Arg230Gly)
5g.146340115A>TCA361621898POU4F3c.688A>T (p.Arg230Trp)
5g.146340116G>ACA128861092POU4F3c.689G>A (p.Arg230Lys)
dbSNP gnomAD v4
5g.146340116G>CCA361621905POU4F3c.689G>C (p.Arg230Thr)
ClinVar dbSNP
5g.146340116G=CA1589086786POU4F3c.689G= (p.Arg230=)
5g.146340116G>TCA361621901POU4F3c.689G>T (p.Arg230Met)
5g.146340117G>ACA447097922POU4F3c.690G>A (p.Arg230=)
5g.146340117G>CCA361621907POU4F3c.690G>C (p.Arg230Ser)
5g.146340117G=CA1589086787POU4F3c.690G= (p.Arg230=)
5g.146340117G>TCA3491182POU4F3c.690G>T (p.Arg230Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.146340118T>ACA361621913POU4F3c.691T>A (p.Phe231Ile)
5g.146340118T>CCA361621916POU4F3c.691T>C (p.Phe231Leu)
5g.146340118T>GCA361621917POU4F3c.691T>G (p.Phe231Val)
5g.146340119T>ACA361621919POU4F3c.692T>A (p.Phe231Tyr)
5g.146340119T>CCA361621920POU4F3c.692T>C (p.Phe231Ser)
gnomAD v4
5g.146340119T>GCA361621922POU4F3c.692T>G (p.Phe231Cys)
5g.146340120C>ACA361621924POU4F3c.693C>A (p.Phe231Leu)
5g.146340120C>GCA361621926POU4F3c.693C>G (p.Phe231Leu)
5g.146340120C>TCA447097924POU4F3c.693C>T (p.Phe231=)
gnomAD v4 COSMIC
5g.146340121G>ACA361621929POU4F3c.694G>A (p.Glu232Lys)
ClinVar dbSNP gnomAD v4
5g.146340121G>CCA361621930POU4F3c.694G>C (p.Glu232Gln)
ClinVar dbSNP gnomAD v4
5g.146340121G>TCA361621931POU4F3c.694G>T (p.Glu232Ter)
ClinVar dbSNP
5g.146340122A>CCA361621935POU4F3c.695A>C (p.Glu232Ala)

Number of alleles fetched