Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.50796343C>ACA395885588CYLD,CYLD-AS2c.2706C>A (p.Asn902Lys)
c.2697C>A (p.Asn899Lys)
c.177+1873C>A
c.2151C>A (p.Asn717Lys)
c.2667C>A (p.Asn889Lys)
c.2677+1915C>A (n.2677+1915C>A)
n.2990C>A
n.2450+5780G>T
n.2824C>A
n.4187+5780G>T
c.2031C>A (p.Asn677Lys)
n.2795C>A
16g.50796343C>GCA395885590CYLD,CYLD-AS2c.2706C>G (p.Asn902Lys)
c.2697C>G (p.Asn899Lys)
c.177+1873C>G
c.2151C>G (p.Asn717Lys)
c.2667C>G (p.Asn889Lys)
c.2677+1915C>G (n.2677+1915C>G)
n.2990C>G
n.2450+5780G>C
n.2824C>G
n.4187+5780G>C
c.2031C>G (p.Asn677Lys)
n.2795C>G
16g.50796343C>TCA495465775CYLD,CYLD-AS2c.2706C>T (p.Asn902=)
c.2697C>T (p.Asn899=)
c.177+1873C>T
c.2151C>T (p.Asn717=)
c.2667C>T (p.Asn889=)
c.2677+1915C>T (n.2677+1915C>T)
n.2990C>T
n.2450+5780G>A
n.2824C>T
n.4187+5780G>A
c.2031C>T (p.Asn677=)
n.2795C>T
 gnomAD v4
16g.50796344A=CA2221882459CYLD,CYLD-AS2c.2707A= (p.Ile903=)
c.2698A= (p.Ile900=)
c.177+1874A=
c.2152A= (p.Ile718=)
c.2668A= (p.Ile890=)
c.2677+1916A= (n.2677+1916A=)
n.2991A=
n.2450+5779T=
n.2825A=
n.4187+5779T=
c.2032A= (p.Ile678=)
n.2796A=
16g.50796344A>CCA395885591CYLD,CYLD-AS2c.2707A>C (p.Ile903Leu)
c.2698A>C (p.Ile900Leu)
c.177+1874A>C
c.2152A>C (p.Ile718Leu)
c.2668A>C (p.Ile890Leu)
c.2677+1916A>C (n.2677+1916A>C)
n.2991A>C
n.2450+5779T>G
n.2825A>C
n.4187+5779T>G
c.2032A>C (p.Ile678Leu)
n.2796A>C
16g.50796344A>GCA8052716CYLD,CYLD-AS2c.2707A>G (p.Ile903Val)
c.2698A>G (p.Ile900Val)
c.177+1874A>G
c.2152A>G (p.Ile718Val)
c.2668A>G (p.Ile890Val)
c.2677+1916A>G (n.2677+1916A>G)
n.2991A>G
n.2450+5779T>C
n.2825A>G
n.4187+5779T>C
c.2032A>G (p.Ile678Val)
n.2796A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.50796344A>TCA395885594CYLD,CYLD-AS2c.2707A>T (p.Ile903Phe)
c.2698A>T (p.Ile900Phe)
c.177+1874A>T
c.2152A>T (p.Ile718Phe)
c.2668A>T (p.Ile890Phe)
c.2677+1916A>T (n.2677+1916A>T)
n.2991A>T
n.2450+5779T>A
n.2825A>T
n.4187+5779T>A
c.2032A>T (p.Ile678Phe)
n.2796A>T
16g.50796345T>ACA395885597CYLD,CYLD-AS2c.2708T>A (p.Ile903Asn)
c.2699T>A (p.Ile900Asn)
c.177+1875T>A
c.2153T>A (p.Ile718Asn)
c.2669T>A (p.Ile890Asn)
c.2677+1917T>A (n.2677+1917T>A)
n.2992T>A
n.2450+5778A>T
n.2826T>A
n.4187+5778A>T
c.2033T>A (p.Ile678Asn)
n.2797T>A
16g.50796345T>CCA395885598CYLD,CYLD-AS2c.2708T>C (p.Ile903Thr)
c.2699T>C (p.Ile900Thr)
c.177+1875T>C
c.2153T>C (p.Ile718Thr)
c.2669T>C (p.Ile890Thr)
c.2677+1917T>C (n.2677+1917T>C)
n.2992T>C
n.2450+5778A>G
n.2826T>C
n.4187+5778A>G
c.2033T>C (p.Ile678Thr)
n.2797T>C
16g.50796345T>GCA395885600CYLD,CYLD-AS2c.2708T>G (p.Ile903Ser)
c.2699T>G (p.Ile900Ser)
c.177+1875T>G
c.2153T>G (p.Ile718Ser)
c.2669T>G (p.Ile890Ser)
c.2677+1917T>G (n.2677+1917T>G)
n.2992T>G
n.2450+5778A>C
n.2826T>G
n.4187+5778A>C
c.2033T>G (p.Ile678Ser)
n.2797T>G
16g.50796346dupCA2695223333CYLD,CYLD-AS2c.2709dup (p.Pro904SerfsTer?)
c.2700dup (p.Pro901SerfsTer?)
c.177+1876dup
c.2154dup (p.Pro719SerfsTer?)
c.2670dup (p.Pro891SerfsTer?)
c.2677+1918dup (n.2677+1918dup)
n.2993dup
n.2450+5778dup
n.2827dup
n.4187+5778dup
c.2034dup (p.Pro679SerfsTer?)
n.2798dup
16g.50796346T>ACA495465806CYLD,CYLD-AS2c.2709T>A (p.Ile903=)
c.2700T>A (p.Ile900=)
c.177+1876T>A
c.2154T>A (p.Ile718=)
c.2670T>A (p.Ile890=)
c.2677+1918T>A (n.2677+1918T>A)
n.2993T>A
n.2450+5777A>T
n.2827T>A
n.4187+5777A>T
c.2034T>A (p.Ile678=)
n.2798T>A
16g.50796346T>CCA495465808CYLD,CYLD-AS2c.2709T>C (p.Ile903=)
c.2700T>C (p.Ile900=)
c.177+1876T>C
c.2154T>C (p.Ile718=)
c.2670T>C (p.Ile890=)
c.2677+1918T>C (n.2677+1918T>C)
n.2993T>C
n.2450+5777A>G
n.2827T>C
n.4187+5777A>G
c.2034T>C (p.Ile678=)
n.2798T>C
16g.50796346T>GCA395885601CYLD,CYLD-AS2c.2709T>G (p.Ile903Met)
c.2700T>G (p.Ile900Met)
c.177+1876T>G
c.2154T>G (p.Ile718Met)
c.2670T>G (p.Ile890Met)
c.2677+1918T>G (n.2677+1918T>G)
n.2993T>G
n.2450+5777A>C
n.2827T>G
n.4187+5777A>C
c.2034T>G (p.Ile678Met)
n.2798T>G
16g.50796347C>ACA395885602CYLD,CYLD-AS2c.2710C>A (p.Pro904Thr)
c.2701C>A (p.Pro901Thr)
c.177+1877C>A
c.2155C>A (p.Pro719Thr)
c.2671C>A (p.Pro891Thr)
c.2677+1919C>A (n.2677+1919C>A)
n.2994C>A
n.2450+5776G>T
n.2828C>A
n.4187+5776G>T
c.2035C>A (p.Pro679Thr)
n.2799C>A
16g.50796347C>GCA395885603CYLD,CYLD-AS2c.2710C>G (p.Pro904Ala)
c.2701C>G (p.Pro901Ala)
c.177+1877C>G
c.2155C>G (p.Pro719Ala)
c.2671C>G (p.Pro891Ala)
c.2677+1919C>G (n.2677+1919C>G)
n.2994C>G
n.2450+5776G>C
n.2828C>G
n.4187+5776G>C
c.2035C>G (p.Pro679Ala)
n.2799C>G
16g.50796347C>TCA395885605CYLD,CYLD-AS2c.2710C>T (p.Pro904Ser)
c.2701C>T (p.Pro901Ser)
c.177+1877C>T
c.2155C>T (p.Pro719Ser)
c.2671C>T (p.Pro891Ser)
c.2677+1919C>T (n.2677+1919C>T)
n.2994C>T
n.2450+5776G>A
n.2828C>T
n.4187+5776G>A
c.2035C>T (p.Pro679Ser)
n.2799C>T
16g.50796348C>ACA395885610CYLD,CYLD-AS2c.2711C>A (p.Pro904His)
c.2702C>A (p.Pro901His)
c.177+1878C>A
c.2156C>A (p.Pro719His)
c.2672C>A (p.Pro891His)
c.2677+1920C>A (n.2677+1920C>A)
n.2995C>A
n.2450+5775G>T
n.2829C>A
n.4187+5775G>T
c.2036C>A (p.Pro679His)
n.2800C>A
16g.50796348C>GCA395885609CYLD,CYLD-AS2c.2711C>G (p.Pro904Arg)
c.2702C>G (p.Pro901Arg)
c.177+1878C>G
c.2156C>G (p.Pro719Arg)
c.2672C>G (p.Pro891Arg)
c.2677+1920C>G (n.2677+1920C>G)
n.2995C>G
n.2450+5775G>C
n.2829C>G
n.4187+5775G>C
c.2036C>G (p.Pro679Arg)
n.2800C>G
16g.50796348C>TCA395885607CYLD,CYLD-AS2c.2711C>T (p.Pro904Leu)
c.2702C>T (p.Pro901Leu)
c.177+1878C>T
c.2156C>T (p.Pro719Leu)
c.2672C>T (p.Pro891Leu)
c.2677+1920C>T (n.2677+1920C>T)
n.2995C>T
n.2450+5775G>A
n.2829C>T
n.4187+5775G>A
c.2036C>T (p.Pro679Leu)
n.2800C>T
 gnomAD v4
16g.50796349delCA2695223334CYLD,CYLD-AS2c.2712del (p.Gln905LysfsTer8)
c.2703del (p.Gln902LysfsTer8)
c.177+1879del
c.2157del (p.Gln720LysfsTer8)
c.2673del (p.Gln892LysfsTer8)
c.2677+1921del (n.2677+1921del)
n.2996del
n.2450+5774del
n.2830del
n.4187+5774del
c.2037del (p.Gln680LysfsTer8)
n.2801del
16g.50796349T>ACA495465843CYLD,CYLD-AS2c.2712T>A (p.Pro904=)
c.2703T>A (p.Pro901=)
c.177+1879T>A
c.2157T>A (p.Pro719=)
c.2673T>A (p.Pro891=)
c.2677+1921T>A (n.2677+1921T>A)
n.2996T>A
n.2450+5774A>T
n.2830T>A
n.4187+5774A>T
c.2037T>A (p.Pro679=)
n.2801T>A
16g.50796349T>CCA495465848CYLD,CYLD-AS2c.2712T>C (p.Pro904=)
c.2703T>C (p.Pro901=)
c.177+1879T>C
c.2157T>C (p.Pro719=)
c.2673T>C (p.Pro891=)
c.2677+1921T>C (n.2677+1921T>C)
n.2996T>C
n.2450+5774A>G
n.2830T>C
n.4187+5774A>G
c.2037T>C (p.Pro679=)
n.2801T>C
16g.50796349T>GCA495465850CYLD,CYLD-AS2c.2712T>G (p.Pro904=)
c.2703T>G (p.Pro901=)
c.177+1879T>G
c.2157T>G (p.Pro719=)
c.2673T>G (p.Pro891=)
c.2677+1921T>G (n.2677+1921T>G)
n.2996T>G
n.2450+5774A>C
n.2830T>G
n.4187+5774A>C
c.2037T>G (p.Pro679=)
n.2801T>G
16g.50796350C>ACA395885612CYLD,CYLD-AS2c.2713C>A (p.Gln905Lys)
c.2704C>A (p.Gln902Lys)
c.177+1880C>A
c.2158C>A (p.Gln720Lys)
c.2674C>A (p.Gln892Lys)
c.2677+1922C>A (n.2677+1922C>A)
n.2997C>A
n.2450+5773G>T
n.2831C>A
n.4187+5773G>T
c.2038C>A (p.Gln680Lys)
n.2802C>A
16g.50796350C>GCA395885616CYLD,CYLD-AS2c.2713C>G (p.Gln905Glu)
c.2704C>G (p.Gln902Glu)
c.177+1880C>G
c.2158C>G (p.Gln720Glu)
c.2674C>G (p.Gln892Glu)
c.2677+1922C>G (n.2677+1922C>G)
n.2997C>G
n.2450+5773G>C
n.2831C>G
n.4187+5773G>C
c.2038C>G (p.Gln680Glu)
n.2802C>G
16g.50796350C>TCA395885614CYLD,CYLD-AS2c.2713C>T (p.Gln905Ter)
c.2704C>T (p.Gln902Ter)
c.177+1880C>T
c.2158C>T (p.Gln720Ter)
c.2674C>T (p.Gln892Ter)
c.2677+1922C>T (n.2677+1922C>T)
n.2997C>T
n.2450+5773G>A
n.2831C>T
n.4187+5773G>A
c.2038C>T (p.Gln680Ter)
n.2802C>T
 dbSNP COSMIC
16g.50796351A>CCA395885619CYLD,CYLD-AS2c.2714A>C (p.Gln905Pro)
c.2705A>C (p.Gln902Pro)
c.177+1881A>C
c.2159A>C (p.Gln720Pro)
c.2675A>C (p.Gln892Pro)
c.2677+1923A>C (n.2677+1923A>C)
n.2998A>C
n.2450+5772T>G
n.2832A>C
n.4187+5772T>G
c.2039A>C (p.Gln680Pro)
n.2803A>C
16g.50796351A>GCA395885622CYLD,CYLD-AS2c.2714A>G (p.Gln905Arg)
c.2705A>G (p.Gln902Arg)
c.177+1881A>G
c.2159A>G (p.Gln720Arg)
c.2675A>G (p.Gln892Arg)
c.2677+1923A>G (n.2677+1923A>G)
n.2998A>G
n.2450+5772T>C
n.2832A>G
n.4187+5772T>C
c.2039A>G (p.Gln680Arg)
n.2803A>G
16g.50796351A>TCA395885621CYLD,CYLD-AS2c.2714A>T (p.Gln905Leu)
c.2705A>T (p.Gln902Leu)
c.177+1881A>T
c.2159A>T (p.Gln720Leu)
c.2675A>T (p.Gln892Leu)
c.2677+1923A>T (n.2677+1923A>T)
n.2998A>T
n.2450+5772T>A
n.2832A>T
n.4187+5772T>A
c.2039A>T (p.Gln680Leu)
n.2803A>T
 dbSNP
16g.50796352A>CCA395885623CYLD,CYLD-AS2c.2715A>C (p.Gln905His)
c.2706A>C (p.Gln902His)
c.177+1882A>C
c.2160A>C (p.Gln720His)
c.2676A>C (p.Gln892His)
c.2677+1924A>C (n.2677+1924A>C)
n.2999A>C
n.2450+5771T>G
n.2833A>C
n.4187+5771T>G
c.2040A>C (p.Gln680His)
n.2804A>C
16g.50796352A>GCA495465906CYLD,CYLD-AS2c.2715A>G (p.Gln905=)
c.2706A>G (p.Gln902=)
c.177+1882A>G
c.2160A>G (p.Gln720=)
c.2676A>G (p.Gln892=)
c.2677+1924A>G (n.2677+1924A>G)
n.2999A>G
n.2450+5771T>C
n.2833A>G
n.4187+5771T>C
c.2040A>G (p.Gln680=)
n.2804A>G
 gnomAD v4
16g.50796352A>TCA395885625CYLD,CYLD-AS2c.2715A>T (p.Gln905His)
c.2706A>T (p.Gln902His)
c.177+1882A>T
c.2160A>T (p.Gln720His)
c.2676A>T (p.Gln892His)
c.2677+1924A>T (n.2677+1924A>T)
n.2999A>T
n.2450+5771T>A
n.2833A>T
n.4187+5771T>A
c.2040A>T (p.Gln680His)
n.2804A>T
16g.50796353G>ACA395885627CYLD,CYLD-AS2c.2716G>A (p.Val906Ile)
c.2707G>A (p.Val903Ile)
c.177+1883G>A
c.2161G>A (p.Val721Ile)
c.2677G>A (p.Val893Ile)
c.2677+1925G>A (n.2677+1925G>A)
n.3000G>A
n.2450+5770C>T
n.2834G>A
n.4187+5770C>T
c.2041G>A (p.Val681Ile)
n.2805G>A
16g.50796353G>CCA395885629CYLD,CYLD-AS2c.2716G>C (p.Val906Leu)
c.2707G>C (p.Val903Leu)
c.177+1883G>C
c.2161G>C (p.Val721Leu)
c.2677G>C (p.Val893Leu)
c.2677+1925G>C (n.2677+1925G>C)
n.3000G>C
n.2450+5770C>G
n.2834G>C
n.4187+5770C>G
c.2041G>C (p.Val681Leu)
n.2805G>C
16g.50796353G>TCA395885628CYLD,CYLD-AS2c.2716G>T (p.Val906Phe)
c.2707G>T (p.Val903Phe)
c.177+1883G>T
c.2161G>T (p.Val721Phe)
c.2677G>T (p.Val893Phe)
c.2677+1925G>T (n.2677+1925G>T)
n.3000G>T
n.2450+5770C>A
n.2834G>T
n.4187+5770C>A
c.2041G>T (p.Val681Phe)
n.2805G>T
16g.50796354T>ACA395885636CYLD,CYLD-AS2c.2717T>A (p.Val906Asp)
c.2708T>A (p.Val903Asp)
c.177+1884T>A
c.2162T>A (p.Val721Asp)
c.2678T>A (p.Val893Asp)
c.2677+1926T>A (n.2677+1926T>A)
n.3001T>A
n.2450+5769A>T
n.2835T>A
n.4187+5769A>T
c.2042T>A (p.Val681Asp)
n.2806T>A
 dbSNP
16g.50796354T>CCA395885640CYLD,CYLD-AS2c.2717T>C (p.Val906Ala)
c.2708T>C (p.Val903Ala)
c.177+1884T>C
c.2162T>C (p.Val721Ala)
c.2678T>C (p.Val893Ala)
c.2677+1926T>C (n.2677+1926T>C)
n.3001T>C
n.2450+5769A>G
n.2835T>C
n.4187+5769A>G
c.2042T>C (p.Val681Ala)
n.2806T>C
16g.50796354T>GCA395885638CYLD,CYLD-AS2c.2717T>G (p.Val906Gly)
c.2708T>G (p.Val903Gly)
c.177+1884T>G
c.2162T>G (p.Val721Gly)
c.2678T>G (p.Val893Gly)
c.2677+1926T>G (n.2677+1926T>G)
n.3001T>G
n.2450+5769A>C
n.2835T>G
n.4187+5769A>C
c.2042T>G (p.Val681Gly)
n.2806T>G
16g.50796355C>ACA495465935CYLD,CYLD-AS2c.2718C>A (p.Val906=)
c.2709C>A (p.Val903=)
c.177+1885C>A
c.2163C>A (p.Val721=)
c.2679C>A (p.Val893=)
c.2677+1927C>A (n.2677+1927C>A)
n.3002C>A
n.2450+5768G>T
n.2836C>A
n.4187+5768G>T
c.2043C>A (p.Val681=)
n.2807C>A
16g.50796355C=CA2221882463CYLD,CYLD-AS2c.2718C= (p.Val906=)
c.2709C= (p.Val903=)
c.177+1885C=
c.2163C= (p.Val721=)
c.2679C= (p.Val893=)
c.2677+1927C= (n.2677+1927C=)
n.3002C=
n.2450+5768G=
n.2836C=
n.4187+5768G=
c.2043C= (p.Val681=)
n.2807C=
16g.50796355C>GCA495465937CYLD,CYLD-AS2c.2718C>G (p.Val906=)
c.2709C>G (p.Val903=)
c.177+1885C>G
c.2163C>G (p.Val721=)
c.2679C>G (p.Val893=)
c.2677+1927C>G (n.2677+1927C>G)
n.3002C>G
n.2450+5768G>C
n.2836C>G
n.4187+5768G>C
c.2043C>G (p.Val681=)
n.2807C>G
 dbSNP
16g.50796355C>TCA495465939CYLD,CYLD-AS2c.2718C>T (p.Val906=)
c.2709C>T (p.Val903=)
c.177+1885C>T
c.2163C>T (p.Val721=)
c.2679C>T (p.Val893=)
c.2677+1927C>T (n.2677+1927C>T)
n.3002C>T
n.2450+5768G>A
n.2836C>T
n.4187+5768G>A
c.2043C>T (p.Val681=)
n.2807C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.50796356A=CA2221882466CYLD,CYLD-AS2c.2719A= (p.Thr907=)
c.2710A= (p.Thr904=)
c.177+1886A=
c.2164A= (p.Thr722=)
c.2680A= (p.Thr894=)
c.2677+1928A= (n.2677+1928A=)
n.3003A=
n.2450+5767T=
n.2837A=
n.4187+5767T=
c.2044A= (p.Thr682=)
n.2808A=
16g.50796356A>CCA395885652CYLD,CYLD-AS2c.2719A>C (p.Thr907Pro)
c.2710A>C (p.Thr904Pro)
c.177+1886A>C
c.2164A>C (p.Thr722Pro)
c.2680A>C (p.Thr894Pro)
c.2677+1928A>C (n.2677+1928A>C)
n.3003A>C
n.2450+5767T>G
n.2837A>C
n.4187+5767T>G
c.2044A>C (p.Thr682Pro)
n.2808A>C
16g.50796356A>GCA395885653CYLD,CYLD-AS2c.2719A>G (p.Thr907Ala)
c.2710A>G (p.Thr904Ala)
c.177+1886A>G
c.2164A>G (p.Thr722Ala)
c.2680A>G (p.Thr894Ala)
c.2677+1928A>G (n.2677+1928A>G)
n.3003A>G
n.2450+5767T>C
n.2837A>G
n.4187+5767T>C
c.2044A>G (p.Thr682Ala)
n.2808A>G
 dbSNP
16g.50796356A>TCA395885654CYLD,CYLD-AS2c.2719A>T (p.Thr907Ser)
c.2710A>T (p.Thr904Ser)
c.177+1886A>T
c.2164A>T (p.Thr722Ser)
c.2680A>T (p.Thr894Ser)
c.2677+1928A>T (n.2677+1928A>T)
n.3003A>T
n.2450+5767T>A
n.2837A>T
n.4187+5767T>A
c.2044A>T (p.Thr682Ser)
n.2808A>T
16g.50796357C>ACA395885656CYLD,CYLD-AS2c.2720C>A (p.Thr907Asn)
c.2711C>A (p.Thr904Asn)
c.177+1887C>A
c.2165C>A (p.Thr722Asn)
c.2681C>A (p.Thr894Asn)
c.2677+1929C>A (n.2677+1929C>A)
n.3004C>A
n.2450+5766G>T
n.2838C>A
n.4187+5766G>T
c.2045C>A (p.Thr682Asn)
n.2809C>A
16g.50796357C>GCA395885658CYLD,CYLD-AS2c.2720C>G (p.Thr907Ser)
c.2711C>G (p.Thr904Ser)
c.177+1887C>G
c.2165C>G (p.Thr722Ser)
c.2681C>G (p.Thr894Ser)
c.2677+1929C>G (n.2677+1929C>G)
n.3004C>G
n.2450+5766G>C
n.2838C>G
n.4187+5766G>C
c.2045C>G (p.Thr682Ser)
n.2809C>G
16g.50796357C>TCA395885659CYLD,CYLD-AS2c.2720C>T (p.Thr907Ile)
c.2711C>T (p.Thr904Ile)
c.177+1887C>T
c.2165C>T (p.Thr722Ile)
c.2681C>T (p.Thr894Ile)
c.2677+1929C>T (n.2677+1929C>T)
n.3004C>T
n.2450+5766G>A
n.2838C>T
n.4187+5766G>A
c.2045C>T (p.Thr682Ile)
n.2809C>T

Number of alleles fetched