Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.76983447_76983457delCA2687718859PEX2c.724_734del (p.Lys242SerfsTer15)
gnomAD v4
8g.76983454T>ACA371556716PEX2c.725A>T (p.Lys242Ile)
8g.76983454T>CCA371556718PEX2c.725A>G (p.Lys242Arg)
8g.76983454T>GCA371556717PEX2c.725A>C (p.Lys242Thr)
8g.76983455T>ACA371556719PEX2c.724A>T (p.Lys242Ter)
8g.76983455T>CCA371556720PEX2c.724A>G (p.Lys242Glu)
8g.76983455T>GCA371556721PEX2c.724A>C (p.Lys242Gln)
8g.76983456G>ACA461773194PEX2c.723C>T (p.Gly241=)
8g.76983456G>CCA461773195PEX2c.723C>G (p.Gly241=)
8g.76983456G>TCA461773196PEX2c.723C>A (p.Gly241=)
8g.76983457C>ACA220656PEX2c.722G>T (p.Gly241Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.76983457C=CA1795350979PEX2c.722G= (p.Gly241=)
8g.76983457C>GCA371556722PEX2c.722G>C (p.Gly241Ala)
8g.76983457C>TCA371556723PEX2c.722G>A (p.Gly241Asp)
dbSNP gnomAD v2 gnomAD v4
8g.76983458C>ACA371556724PEX2c.721G>T (p.Gly241Cys)
8g.76983458C>GCA371556725PEX2c.721G>C (p.Gly241Arg)
8g.76983458C>TCA371556726PEX2c.721G>A (p.Gly241Ser)
dbSNP
8g.76983459A=CA1795350983PEX2c.720T= (p.Ser240=)
8g.76983459A>CCA371556727PEX2c.720T>G (p.Ser240Arg)
8g.76983459A>GCA179988256PEX2c.720T>C (p.Ser240=)
ClinVar dbSNP gnomAD v3 gnomAD v4
8g.76983459A>TCA371556728PEX2c.720T>A (p.Ser240Arg)
8g.76983460C>ACA371556731PEX2c.719G>T (p.Ser240Ile)
8g.76983460C>GCA371556730PEX2c.719G>C (p.Ser240Thr)
8g.76983460C>TCA371556729PEX2c.719G>A (p.Ser240Asn)
gnomAD v4
8g.76983461T>ACA371556732PEX2c.718A>T (p.Ser240Cys)
8g.76983461T>CCA371556733PEX2c.718A>G (p.Ser240Gly)
8g.76983461T>GCA371556734PEX2c.718A>C (p.Ser240Arg)
ClinVar
8g.76983462G>ACA461773197PEX2c.717C>T (p.Thr239=)
ClinVar dbSNP gnomAD v4
8g.76983462G>CCA461773199PEX2c.717C>G (p.Thr239=)
8g.76983462G>TCA461773200PEX2c.717C>A (p.Thr239=)
8g.76983463G>ACA371556735PEX2c.716C>T (p.Thr239Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.76983463G>CCA371556736PEX2c.716C>G (p.Thr239Ser)
8g.76983463G=CA1795350989PEX2c.716C= (p.Thr239=)
8g.76983463G>TCA371556737PEX2c.716C>A (p.Thr239Asn)
8g.76983464T>ACA371556738PEX2c.715A>T (p.Thr239Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
8g.76983464T>CCA371556739PEX2c.715A>G (p.Thr239Ala)
8g.76983464T>GCA371556740PEX2c.715A>C (p.Thr239Pro)
8g.76983464T=CA1795350995PEX2c.715A= (p.Thr239=)
8g.76983465G>ACA461773201PEX2c.714C>T (p.Ala238=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.76983465G>CCA461773202PEX2c.714C>G (p.Ala238=)
8g.76983465G=CA1795350998PEX2c.714C= (p.Ala238=)
8g.76983465G>TCA461773203PEX2c.714C>A (p.Ala238=)
8g.76983466G>ACA371556741PEX2c.713C>T (p.Ala238Val)
8g.76983466G>CCA371556742PEX2c.713C>G (p.Ala238Gly)
8g.76983466G>TCA371556743PEX2c.713C>A (p.Ala238Asp)
gnomAD v4
8g.76983467C>ACA371556746PEX2c.712G>T (p.Ala238Ser)
8g.76983467C>GCA371556745PEX2c.712G>C (p.Ala238Pro)
8g.76983467C>TCA371556744PEX2c.712G>A (p.Ala238Thr)
8g.76983468T>ACA371556747PEX2c.711A>T (p.Leu237Phe)
8g.76983468T>CCA461773208PEX2c.711A>G (p.Leu237=)

Number of alleles fetched