Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.85271596delCA16616868ZNF711c.2192del (p.Phe731SerfsTer7)
c.2054del (p.Phe685SerfsTer7)
c.2204del (p.Phe735SerfsTer7)
c.2066del (p.Phe689SerfsTer7)
ClinVar dbSNP
Xg.85271596T>ACA413777472ZNF711c.2192T>A (p.Phe731Tyr)
c.2054T>A (p.Phe685Tyr)
c.2204T>A (p.Phe735Tyr)
c.2066T>A (p.Phe689Tyr)
Xg.85271596T>CCA413777475ZNF711c.2192T>C (p.Phe731Ser)
c.2054T>C (p.Phe685Ser)
c.2204T>C (p.Phe735Ser)
c.2066T>C (p.Phe689Ser)
Xg.85271596T>GCA413777476ZNF711c.2192T>G (p.Phe731Cys)
c.2054T>G (p.Phe685Cys)
c.2204T>G (p.Phe735Cys)
c.2066T>G (p.Phe689Cys)
Xg.85271597C>ACA413777478ZNF711c.2193C>A (p.Phe731Leu)
c.2055C>A (p.Phe685Leu)
c.2205C>A (p.Phe735Leu)
c.2067C>A (p.Phe689Leu)
Xg.85271597C=CA2442182356ZNF711c.2193C= (p.Phe731=)
c.2055C= (p.Phe685=)
c.2205C= (p.Phe735=)
c.2067C= (p.Phe689=)
Xg.85271597C>GCA413777480ZNF711c.2193C>G (p.Phe731Leu)
c.2055C>G (p.Phe685Leu)
c.2205C>G (p.Phe735Leu)
c.2067C>G (p.Phe689Leu)
Xg.85271597C>TCA517517265ZNF711c.2193C>T (p.Phe731=)
c.2055C>T (p.Phe685=)
c.2205C>T (p.Phe735=)
c.2067C>T (p.Phe689=)
dbSNP gnomAD v2 gnomAD v4
Xg.85271598A=CA2442182357ZNF711c.2194A= (p.Arg732=)
c.2056A= (p.Arg686=)
c.2206A= (p.Arg736=)
c.2068A= (p.Arg690=)
Xg.85271598A>CCA517517267ZNF711c.2194A>C (p.Arg732=)
c.2056A>C (p.Arg686=)
c.2206A>C (p.Arg736=)
c.2068A>C (p.Arg690=)
Xg.85271598A>GCA332538529ZNF711c.2194A>G (p.Arg732Gly)
c.2056A>G (p.Arg686Gly)
c.2206A>G (p.Arg736Gly)
c.2068A>G (p.Arg690Gly)
dbSNP gnomAD v4
Xg.85271598A>TCA413777484ZNF711c.2194A>T (p.Arg732Ter)
c.2056A>T (p.Arg686Ter)
c.2206A>T (p.Arg736Ter)
c.2068A>T (p.Arg690Ter)
Xg.85271599G>ACA413777487ZNF711c.2195G>A (p.Arg732Lys)
c.2057G>A (p.Arg686Lys)
c.2207G>A (p.Arg736Lys)
c.2069G>A (p.Arg690Lys)
Xg.85271599G>CCA413777489ZNF711c.2195G>C (p.Arg732Thr)
c.2057G>C (p.Arg686Thr)
c.2207G>C (p.Arg736Thr)
c.2069G>C (p.Arg690Thr)
Xg.85271599G>TCA413777490ZNF711c.2195G>T (p.Arg732Ile)
c.2057G>T (p.Arg686Ile)
c.2207G>T (p.Arg736Ile)
c.2069G>T (p.Arg690Ile)
Xg.85271600A>CCA413777493ZNF711c.2196A>C (p.Arg732Ser)
c.2058A>C (p.Arg686Ser)
c.2208A>C (p.Arg736Ser)
c.2070A>C (p.Arg690Ser)
Xg.85271600A>GCA517517270ZNF711c.2196A>G (p.Arg732=)
c.2058A>G (p.Arg686=)
c.2208A>G (p.Arg736=)
c.2070A>G (p.Arg690=)
gnomAD v4
Xg.85271600A>TCA413777494ZNF711c.2196A>T (p.Arg732Ser)
c.2058A>T (p.Arg686Ser)
c.2208A>T (p.Arg736Ser)
c.2070A>T (p.Arg690Ser)
Xg.85271601C>ACA413777496ZNF711c.2197C>A (p.Gln733Lys)
c.2059C>A (p.Gln687Lys)
c.2209C>A (p.Gln737Lys)
c.2071C>A (p.Gln691Lys)
Xg.85271601C=CA2442182358ZNF711c.2197C= (p.Gln733=)
c.2059C= (p.Gln687=)
c.2209C= (p.Gln737=)
c.2071C= (p.Gln691=)
Xg.85271601C>GCA413777498ZNF711c.2197C>G (p.Gln733Glu)
c.2059C>G (p.Gln687Glu)
c.2209C>G (p.Gln737Glu)
c.2071C>G (p.Gln691Glu)
dbSNP
Xg.85271601C>TCA413777499ZNF711c.2197C>T (p.Gln733Ter)
c.2059C>T (p.Gln687Ter)
c.2209C>T (p.Gln737Ter)
c.2071C>T (p.Gln691Ter)
gnomAD v4
Xg.85271602A>CCA413777502ZNF711c.2198A>C (p.Gln733Pro)
c.2060A>C (p.Gln687Pro)
c.2210A>C (p.Gln737Pro)
c.2072A>C (p.Gln691Pro)
Xg.85271602A>GCA413777504ZNF711c.2198A>G (p.Gln733Arg)
c.2060A>G (p.Gln687Arg)
c.2210A>G (p.Gln737Arg)
c.2072A>G (p.Gln691Arg)
Xg.85271602A>TCA413777507ZNF711c.2198A>T (p.Gln733Leu)
c.2060A>T (p.Gln687Leu)
c.2210A>T (p.Gln737Leu)
c.2072A>T (p.Gln691Leu)
Xg.85271603A>CCA413777510ZNF711c.2199A>C (p.Gln733His)
c.2061A>C (p.Gln687His)
c.2211A>C (p.Gln737His)
c.2073A>C (p.Gln691His)
Xg.85271603A>GCA517517274ZNF711c.2199A>G (p.Gln733=)
c.2061A>G (p.Gln687=)
c.2211A>G (p.Gln737=)
c.2073A>G (p.Gln691=)
Xg.85271603A>TCA413777512ZNF711c.2199A>T (p.Gln733His)
c.2061A>T (p.Gln687His)
c.2211A>T (p.Gln737His)
c.2073A>T (p.Gln691His)
Xg.85271604C>ACA413777516ZNF711c.2200C>A (p.Gln734Lys)
c.2062C>A (p.Gln688Lys)
c.2212C>A (p.Gln738Lys)
c.2074C>A (p.Gln692Lys)
Xg.85271604C>GCA413777518ZNF711c.2200C>G (p.Gln734Glu)
c.2062C>G (p.Gln688Glu)
c.2212C>G (p.Gln738Glu)
c.2074C>G (p.Gln692Glu)
Xg.85271604C>TCA413777514ZNF711c.2200C>T (p.Gln734Ter)
c.2062C>T (p.Gln688Ter)
c.2212C>T (p.Gln738Ter)
c.2074C>T (p.Gln692Ter)
Xg.85271605A>CCA413777520ZNF711c.2201A>C (p.Gln734Pro)
c.2063A>C (p.Gln688Pro)
c.2213A>C (p.Gln738Pro)
c.2075A>C (p.Gln692Pro)
Xg.85271605A>GCA413777523ZNF711c.2201A>G (p.Gln734Arg)
c.2063A>G (p.Gln688Arg)
c.2213A>G (p.Gln738Arg)
c.2075A>G (p.Gln692Arg)
Xg.85271605A>TCA413777524ZNF711c.2201A>T (p.Gln734Leu)
c.2063A>T (p.Gln688Leu)
c.2213A>T (p.Gln738Leu)
c.2075A>T (p.Gln692Leu)
Xg.85271606A>CCA413777527ZNF711c.2202A>C (p.Gln734His)
c.2064A>C (p.Gln688His)
c.2214A>C (p.Gln738His)
c.2076A>C (p.Gln692His)
Xg.85271606A>GCA517517277ZNF711c.2202A>G (p.Gln734=)
c.2064A>G (p.Gln688=)
c.2214A>G (p.Gln738=)
c.2076A>G (p.Gln692=)
Xg.85271606A>TCA413777529ZNF711c.2202A>T (p.Gln734His)
c.2064A>T (p.Gln688His)
c.2214A>T (p.Gln738His)
c.2076A>T (p.Gln692His)
Xg.85271607A>CCA413777534ZNF711c.2203A>C (p.Asn735His)
c.2065A>C (p.Asn689His)
c.2215A>C (p.Asn739His)
c.2077A>C (p.Asn693His)
Xg.85271607A>GCA413777532ZNF711c.2203A>G (p.Asn735Asp)
c.2065A>G (p.Asn689Asp)
c.2215A>G (p.Asn739Asp)
c.2077A>G (p.Asn693Asp)
Xg.85271607A>TCA413777533ZNF711c.2203A>T (p.Asn735Tyr)
c.2065A>T (p.Asn689Tyr)
c.2215A>T (p.Asn739Tyr)
c.2077A>T (p.Asn693Tyr)
Xg.85271608A>CCA413777536ZNF711c.2204A>C (p.Asn735Thr)
c.2066A>C (p.Asn689Thr)
c.2216A>C (p.Asn739Thr)
c.2078A>C (p.Asn693Thr)
Xg.85271608A>GCA413777537ZNF711c.2204A>G (p.Asn735Ser)
c.2066A>G (p.Asn689Ser)
c.2216A>G (p.Asn739Ser)
c.2078A>G (p.Asn693Ser)
Xg.85271608A>TCA413777540ZNF711c.2204A>T (p.Asn735Ile)
c.2066A>T (p.Asn689Ile)
c.2216A>T (p.Asn739Ile)
c.2078A>T (p.Asn693Ile)
Xg.85271609T>ACA413777542ZNF711c.2205T>A (p.Asn735Lys)
c.2067T>A (p.Asn689Lys)
c.2217T>A (p.Asn739Lys)
c.2079T>A (p.Asn693Lys)
Xg.85271609T>CCA517517284ZNF711c.2205T>C (p.Asn735=)
c.2067T>C (p.Asn689=)
c.2217T>C (p.Asn739=)
c.2079T>C (p.Asn693=)
Xg.85271609T>GCA413777544ZNF711c.2205T>G (p.Asn735Lys)
c.2067T>G (p.Asn689Lys)
c.2217T>G (p.Asn739Lys)
c.2079T>G (p.Asn693Lys)
Xg.85271610G>ACA413777546ZNF711c.2206G>A (p.Glu736Lys)
c.2068G>A (p.Glu690Lys)
c.2218G>A (p.Glu740Lys)
c.2080G>A (p.Glu694Lys)
Xg.85271610G>CCA413777550ZNF711c.2206G>C (p.Glu736Gln)
c.2068G>C (p.Glu690Gln)
c.2218G>C (p.Glu740Gln)
c.2080G>C (p.Glu694Gln)
Xg.85271610G>TCA413777548ZNF711c.2206G>T (p.Glu736Ter)
c.2068G>T (p.Glu690Ter)
c.2218G>T (p.Glu740Ter)
c.2080G>T (p.Glu694Ter)
Xg.85271611A>CCA413777553ZNF711c.2207A>C (p.Glu736Ala)
c.2069A>C (p.Glu690Ala)
c.2219A>C (p.Glu740Ala)
c.2081A>C (p.Glu694Ala)

Number of alleles fetched