Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.123291262_123291264delCA2586973104ADCY5c.1857_1859del (p.Asp619del)
c.2145_2147del (p.Asp715del)
n.1583_1585del
c.3255_3257del (p.Asp1085del)
c.3180_3182del (p.Asp1060del)
c.2130_2132del (p.Asp710del)
c.2154_2156del (p.Asp718del)
c.2205_2207del (p.Asp735del)
c.1932_1934del (p.Asp644del)
c.2256_2258del (p.Asp752del)
c.2166_2168del (p.Asp722del)
c.2157_2159del (p.Asp719del)
3g.123291260A>CCA354223649ADCY5c.1857T>G (p.Asp619Glu)
c.2145T>G (p.Asp715Glu)
n.1583T>G
c.3255T>G (p.Asp1085Glu)
c.3180T>G (p.Asp1060Glu)
c.2130T>G (p.Asp710Glu)
c.2154T>G (p.Asp718Glu)
c.2205T>G (p.Asp735Glu)
c.1932T>G (p.Asp644Glu)
c.2256T>G (p.Asp752Glu)
c.2166T>G (p.Asp722Glu)
c.2157T>G (p.Asp719Glu)
ClinVar dbSNP gnomAD v4
3g.123291260A>GCA435431418ADCY5c.1857T>C (p.Asp619=)
c.2145T>C (p.Asp715=)
n.1583T>C
c.3255T>C (p.Asp1085=)
c.3180T>C (p.Asp1060=)
c.2130T>C (p.Asp710=)
c.2154T>C (p.Asp718=)
c.2205T>C (p.Asp735=)
c.1932T>C (p.Asp644=)
c.2256T>C (p.Asp752=)
c.2166T>C (p.Asp722=)
c.2157T>C (p.Asp719=)
3g.123291260A>TCA354223650ADCY5c.1857T>A (p.Asp619Glu)
c.2145T>A (p.Asp715Glu)
n.1583T>A
c.3255T>A (p.Asp1085Glu)
c.3180T>A (p.Asp1060Glu)
c.2130T>A (p.Asp710Glu)
c.2154T>A (p.Asp718Glu)
c.2205T>A (p.Asp735Glu)
c.1932T>A (p.Asp644Glu)
c.2256T>A (p.Asp752Glu)
c.2166T>A (p.Asp722Glu)
c.2157T>A (p.Asp719Glu)
3g.123291261T>ACA354223653ADCY5c.1856A>T (p.Asp619Val)
c.2144A>T (p.Asp715Val)
n.1582A>T
c.3254A>T (p.Asp1085Val)
c.3179A>T (p.Asp1060Val)
c.2129A>T (p.Asp710Val)
c.2153A>T (p.Asp718Val)
c.2204A>T (p.Asp735Val)
c.1931A>T (p.Asp644Val)
c.2255A>T (p.Asp752Val)
c.2165A>T (p.Asp722Val)
c.2156A>T (p.Asp719Val)
3g.123291261T>CCA354223652ADCY5c.1856A>G (p.Asp619Gly)
c.2144A>G (p.Asp715Gly)
n.1582A>G
c.3254A>G (p.Asp1085Gly)
c.3179A>G (p.Asp1060Gly)
c.2129A>G (p.Asp710Gly)
c.2153A>G (p.Asp718Gly)
c.2204A>G (p.Asp735Gly)
c.1931A>G (p.Asp644Gly)
c.2255A>G (p.Asp752Gly)
c.2165A>G (p.Asp722Gly)
c.2156A>G (p.Asp719Gly)
gnomAD v4
3g.123291261T>GCA354223651ADCY5c.1856A>C (p.Asp619Ala)
c.2144A>C (p.Asp715Ala)
n.1582A>C
c.3254A>C (p.Asp1085Ala)
c.3179A>C (p.Asp1060Ala)
c.2129A>C (p.Asp710Ala)
c.2153A>C (p.Asp718Ala)
c.2204A>C (p.Asp735Ala)
c.1931A>C (p.Asp644Ala)
c.2255A>C (p.Asp752Ala)
c.2165A>C (p.Asp722Ala)
c.2156A>C (p.Asp719Ala)
3g.123291262C>ACA354223654ADCY5c.1855G>T (p.Asp619Tyr)
c.2143G>T (p.Asp715Tyr)
n.1581G>T
c.3253G>T (p.Asp1085Tyr)
c.3178G>T (p.Asp1060Tyr)
c.2128G>T (p.Asp710Tyr)
c.2152G>T (p.Asp718Tyr)
c.2203G>T (p.Asp735Tyr)
c.1930G>T (p.Asp644Tyr)
c.2254G>T (p.Asp752Tyr)
c.2164G>T (p.Asp722Tyr)
c.2155G>T (p.Asp719Tyr)
3g.123291262C>GCA354223656ADCY5c.1855G>C (p.Asp619His)
c.2143G>C (p.Asp715His)
n.1581G>C
c.3253G>C (p.Asp1085His)
c.3178G>C (p.Asp1060His)
c.2128G>C (p.Asp710His)
c.2152G>C (p.Asp718His)
c.2203G>C (p.Asp735His)
c.1930G>C (p.Asp644His)
c.2254G>C (p.Asp752His)
c.2164G>C (p.Asp722His)
c.2155G>C (p.Asp719His)
3g.123291262C>TCA354223655ADCY5c.1855G>A (p.Asp619Asn)
c.2143G>A (p.Asp715Asn)
n.1581G>A
c.3253G>A (p.Asp1085Asn)
c.3178G>A (p.Asp1060Asn)
c.2128G>A (p.Asp710Asn)
c.2152G>A (p.Asp718Asn)
c.2203G>A (p.Asp735Asn)
c.1930G>A (p.Asp644Asn)
c.2254G>A (p.Asp752Asn)
c.2164G>A (p.Asp722Asn)
c.2155G>A (p.Asp719Asn)
3g.123291263A>CCA354223657ADCY5c.1854T>G (p.Asn618Lys)
c.2142T>G (p.Asn714Lys)
n.1580T>G
c.3252T>G (p.Asn1084Lys)
c.3177T>G (p.Asn1059Lys)
c.2127T>G (p.Asn709Lys)
c.2151T>G (p.Asn717Lys)
c.2202T>G (p.Asn734Lys)
c.1929T>G (p.Asn643Lys)
c.2253T>G (p.Asn751Lys)
c.2163T>G (p.Asn721Lys)
c.2154T>G (p.Asn718Lys)
3g.123291263A>GCA435431420ADCY5c.1854T>C (p.Asn618=)
c.2142T>C (p.Asn714=)
n.1580T>C
c.3252T>C (p.Asn1084=)
c.3177T>C (p.Asn1059=)
c.2127T>C (p.Asn709=)
c.2151T>C (p.Asn717=)
c.2202T>C (p.Asn734=)
c.1929T>C (p.Asn643=)
c.2253T>C (p.Asn751=)
c.2163T>C (p.Asn721=)
c.2154T>C (p.Asn718=)
gnomAD v4
3g.123291263A>TCA354223658ADCY5c.1854T>A (p.Asn618Lys)
c.2142T>A (p.Asn714Lys)
n.1580T>A
c.3252T>A (p.Asn1084Lys)
c.3177T>A (p.Asn1059Lys)
c.2127T>A (p.Asn709Lys)
c.2151T>A (p.Asn717Lys)
c.2202T>A (p.Asn734Lys)
c.1929T>A (p.Asn643Lys)
c.2253T>A (p.Asn751Lys)
c.2163T>A (p.Asn721Lys)
c.2154T>A (p.Asn718Lys)
3g.123291264T>ACA354223659ADCY5c.1853A>T (p.Asn618Ile)
c.2141A>T (p.Asn714Ile)
n.1579A>T
c.3251A>T (p.Asn1084Ile)
c.3176A>T (p.Asn1059Ile)
c.2126A>T (p.Asn709Ile)
c.2150A>T (p.Asn717Ile)
c.2201A>T (p.Asn734Ile)
c.1928A>T (p.Asn643Ile)
c.2252A>T (p.Asn751Ile)
c.2162A>T (p.Asn721Ile)
c.2153A>T (p.Asn718Ile)
3g.123291264T>CCA2576833ADCY5c.1853A>G (p.Asn618Ser)
c.2141A>G (p.Asn714Ser)
n.1579A>G
c.3251A>G (p.Asn1084Ser)
c.3176A>G (p.Asn1059Ser)
c.2126A>G (p.Asn709Ser)
c.2150A>G (p.Asn717Ser)
c.2201A>G (p.Asn734Ser)
c.1928A>G (p.Asn643Ser)
c.2252A>G (p.Asn751Ser)
c.2162A>G (p.Asn721Ser)
c.2153A>G (p.Asn718Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.123291264T>GCA354223660ADCY5c.1853A>C (p.Asn618Thr)
c.2141A>C (p.Asn714Thr)
n.1579A>C
c.3251A>C (p.Asn1084Thr)
c.3176A>C (p.Asn1059Thr)
c.2126A>C (p.Asn709Thr)
c.2150A>C (p.Asn717Thr)
c.2201A>C (p.Asn734Thr)
c.1928A>C (p.Asn643Thr)
c.2252A>C (p.Asn751Thr)
c.2162A>C (p.Asn721Thr)
c.2153A>C (p.Asn718Thr)
3g.123291264T=CA1398330414ADCY5c.1853A= (p.Asn618=)
c.2141A= (p.Asn714=)
n.1579A=
c.3251A= (p.Asn1084=)
c.3176A= (p.Asn1059=)
c.2126A= (p.Asn709=)
c.2150A= (p.Asn717=)
c.2201A= (p.Asn734=)
c.1928A= (p.Asn643=)
c.2252A= (p.Asn751=)
c.2162A= (p.Asn721=)
c.2153A= (p.Asn718=)
3g.123291265T>ACA354223661ADCY5c.1852A>T (p.Asn618Tyr)
c.2140A>T (p.Asn714Tyr)
n.1578A>T
c.3250A>T (p.Asn1084Tyr)
c.3175A>T (p.Asn1059Tyr)
c.2125A>T (p.Asn709Tyr)
c.2149A>T (p.Asn717Tyr)
c.2200A>T (p.Asn734Tyr)
c.1927A>T (p.Asn643Tyr)
c.2251A>T (p.Asn751Tyr)
c.2161A>T (p.Asn721Tyr)
c.2152A>T (p.Asn718Tyr)
3g.123291265T>CCA354223662ADCY5c.1852A>G (p.Asn618Asp)
c.2140A>G (p.Asn714Asp)
n.1578A>G
c.3250A>G (p.Asn1084Asp)
c.3175A>G (p.Asn1059Asp)
c.2125A>G (p.Asn709Asp)
c.2149A>G (p.Asn717Asp)
c.2200A>G (p.Asn734Asp)
c.1927A>G (p.Asn643Asp)
c.2251A>G (p.Asn751Asp)
c.2161A>G (p.Asn721Asp)
c.2152A>G (p.Asn718Asp)
3g.123291265T>GCA354223663ADCY5c.1852A>C (p.Asn618His)
c.2140A>C (p.Asn714His)
n.1578A>C
c.3250A>C (p.Asn1084His)
c.3175A>C (p.Asn1059His)
c.2125A>C (p.Asn709His)
c.2149A>C (p.Asn717His)
c.2200A>C (p.Asn734His)
c.1927A>C (p.Asn643His)
c.2251A>C (p.Asn751His)
c.2161A>C (p.Asn721His)
c.2152A>C (p.Asn718His)
3g.123291266G>ACA435431423ADCY5c.1851C>T (p.Arg617=)
c.2139C>T (p.Arg713=)
n.1577C>T
c.3249C>T (p.Arg1083=)
c.3174C>T (p.Arg1058=)
c.2124C>T (p.Arg708=)
c.2148C>T (p.Arg716=)
c.2199C>T (p.Arg733=)
c.1926C>T (p.Arg642=)
c.2250C>T (p.Arg750=)
c.2160C>T (p.Arg720=)
c.2151C>T (p.Arg717=)
3g.123291266G>CCA435431425ADCY5c.1851C>G (p.Arg617=)
c.2139C>G (p.Arg713=)
n.1577C>G
c.3249C>G (p.Arg1083=)
c.3174C>G (p.Arg1058=)
c.2124C>G (p.Arg708=)
c.2148C>G (p.Arg716=)
c.2199C>G (p.Arg733=)
c.1926C>G (p.Arg642=)
c.2250C>G (p.Arg750=)
c.2160C>G (p.Arg720=)
c.2151C>G (p.Arg717=)
3g.123291266G>TCA435431424ADCY5c.1851C>A (p.Arg617=)
c.2139C>A (p.Arg713=)
n.1577C>A
c.3249C>A (p.Arg1083=)
c.3174C>A (p.Arg1058=)
c.2124C>A (p.Arg708=)
c.2148C>A (p.Arg716=)
c.2199C>A (p.Arg733=)
c.1926C>A (p.Arg642=)
c.2250C>A (p.Arg750=)
c.2160C>A (p.Arg720=)
c.2151C>A (p.Arg717=)
3g.123291267C>ACA354223664ADCY5c.1850G>T (p.Arg617Leu)
c.2138G>T (p.Arg713Leu)
n.1576G>T
c.3248G>T (p.Arg1083Leu)
c.3173G>T (p.Arg1058Leu)
c.2123G>T (p.Arg708Leu)
c.2147G>T (p.Arg716Leu)
c.2198G>T (p.Arg733Leu)
c.1925G>T (p.Arg642Leu)
c.2249G>T (p.Arg750Leu)
c.2159G>T (p.Arg720Leu)
c.2150G>T (p.Arg717Leu)
dbSNP gnomAD v4
3g.123291267C=CA1398330415ADCY5c.1850G= (p.Arg617=)
c.2138G= (p.Arg713=)
n.1576G=
c.3248G= (p.Arg1083=)
c.3173G= (p.Arg1058=)
c.2123G= (p.Arg708=)
c.2147G= (p.Arg716=)
c.2198G= (p.Arg733=)
c.1925G= (p.Arg642=)
c.2249G= (p.Arg750=)
c.2159G= (p.Arg720=)
c.2150G= (p.Arg717=)
3g.123291267C>GCA354223665ADCY5c.1850G>C (p.Arg617Pro)
c.2138G>C (p.Arg713Pro)
n.1576G>C
c.3248G>C (p.Arg1083Pro)
c.3173G>C (p.Arg1058Pro)
c.2123G>C (p.Arg708Pro)
c.2147G>C (p.Arg716Pro)
c.2198G>C (p.Arg733Pro)
c.1925G>C (p.Arg642Pro)
c.2249G>C (p.Arg750Pro)
c.2159G>C (p.Arg720Pro)
c.2150G>C (p.Arg717Pro)
3g.123291267C>TCA2576834ADCY5c.1850G>A (p.Arg617His)
c.2138G>A (p.Arg713His)
n.1576G>A
c.3248G>A (p.Arg1083His)
c.3173G>A (p.Arg1058His)
c.2123G>A (p.Arg708His)
c.2147G>A (p.Arg716His)
c.2198G>A (p.Arg733His)
c.1925G>A (p.Arg642His)
c.2249G>A (p.Arg750His)
c.2159G>A (p.Arg720His)
c.2150G>A (p.Arg717His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.123291268G>ACA2576835ADCY5c.1849C>T (p.Arg617Cys)
c.2137C>T (p.Arg713Cys)
n.1575C>T
c.3247C>T (p.Arg1083Cys)
c.3172C>T (p.Arg1058Cys)
c.2122C>T (p.Arg708Cys)
c.2146C>T (p.Arg716Cys)
c.2197C>T (p.Arg733Cys)
c.1924C>T (p.Arg642Cys)
c.2248C>T (p.Arg750Cys)
c.2158C>T (p.Arg720Cys)
c.2149C>T (p.Arg717Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.123291268G>CCA354223667ADCY5c.1849C>G (p.Arg617Gly)
c.2137C>G (p.Arg713Gly)
n.1575C>G
c.3247C>G (p.Arg1083Gly)
c.3172C>G (p.Arg1058Gly)
c.2122C>G (p.Arg708Gly)
c.2146C>G (p.Arg716Gly)
c.2197C>G (p.Arg733Gly)
c.1924C>G (p.Arg642Gly)
c.2248C>G (p.Arg750Gly)
c.2158C>G (p.Arg720Gly)
c.2149C>G (p.Arg717Gly)
3g.123291268G=CA1398330416ADCY5c.1849C= (p.Arg617=)
c.2137C= (p.Arg713=)
n.1575C=
c.3247C= (p.Arg1083=)
c.3172C= (p.Arg1058=)
c.2122C= (p.Arg708=)
c.2146C= (p.Arg716=)
c.2197C= (p.Arg733=)
c.1924C= (p.Arg642=)
c.2248C= (p.Arg750=)
c.2158C= (p.Arg720=)
c.2149C= (p.Arg717=)
3g.123291268G>TCA354223666ADCY5c.1849C>A (p.Arg617Ser)
c.2137C>A (p.Arg713Ser)
n.1575C>A
c.3247C>A (p.Arg1083Ser)
c.3172C>A (p.Arg1058Ser)
c.2122C>A (p.Arg708Ser)
c.2146C>A (p.Arg716Ser)
c.2197C>A (p.Arg733Ser)
c.1924C>A (p.Arg642Ser)
c.2248C>A (p.Arg750Ser)
c.2158C>A (p.Arg720Ser)
c.2149C>A (p.Arg717Ser)
3g.123291269C>ACA435431253ADCY5c.1848G>T (p.Arg616=)
c.2136G>T (p.Arg712=)
n.1574G>T
c.3246G>T (p.Arg1082=)
c.3171G>T (p.Arg1057=)
c.2121G>T (p.Arg707=)
c.2145G>T (p.Arg715=)
c.2196G>T (p.Arg732=)
c.1923G>T (p.Arg641=)
c.2247G>T (p.Arg749=)
c.2157G>T (p.Arg719=)
c.2148G>T (p.Arg716=)
dbSNP gnomAD v3 gnomAD v4
3g.123291269C=CA1398330417ADCY5c.1848G= (p.Arg616=)
c.2136G= (p.Arg712=)
n.1574G=
c.3246G= (p.Arg1082=)
c.3171G= (p.Arg1057=)
c.2121G= (p.Arg707=)
c.2145G= (p.Arg715=)
c.2196G= (p.Arg732=)
c.1923G= (p.Arg641=)
c.2247G= (p.Arg749=)
c.2157G= (p.Arg719=)
c.2148G= (p.Arg716=)
3g.123291269C>GCA435431254ADCY5c.1848G>C (p.Arg616=)
c.2136G>C (p.Arg712=)
n.1574G>C
c.3246G>C (p.Arg1082=)
c.3171G>C (p.Arg1057=)
c.2121G>C (p.Arg707=)
c.2145G>C (p.Arg715=)
c.2196G>C (p.Arg732=)
c.1923G>C (p.Arg641=)
c.2247G>C (p.Arg749=)
c.2157G>C (p.Arg719=)
c.2148G>C (p.Arg716=)
3g.123291269C>TCA435431255ADCY5c.1848G>A (p.Arg616=)
c.2136G>A (p.Arg712=)
n.1574G>A
c.3246G>A (p.Arg1082=)
c.3171G>A (p.Arg1057=)
c.2121G>A (p.Arg707=)
c.2145G>A (p.Arg715=)
c.2196G>A (p.Arg732=)
c.1923G>A (p.Arg641=)
c.2247G>A (p.Arg749=)
c.2157G>A (p.Arg719=)
c.2148G>A (p.Arg716=)
3g.123291270C>ACA354223668ADCY5c.1847G>T (p.Arg616Leu)
c.2135G>T (p.Arg712Leu)
n.1573G>T
c.3245G>T (p.Arg1082Leu)
c.3170G>T (p.Arg1057Leu)
c.2120G>T (p.Arg707Leu)
c.2144G>T (p.Arg715Leu)
c.2195G>T (p.Arg732Leu)
c.1922G>T (p.Arg641Leu)
c.2246G>T (p.Arg749Leu)
c.2156G>T (p.Arg719Leu)
c.2147G>T (p.Arg716Leu)
3g.123291270C=CA1398330418ADCY5c.1847G= (p.Arg616=)
c.2135G= (p.Arg712=)
n.1573G=
c.3245G= (p.Arg1082=)
c.3170G= (p.Arg1057=)
c.2120G= (p.Arg707=)
c.2144G= (p.Arg715=)
c.2195G= (p.Arg732=)
c.1922G= (p.Arg641=)
c.2246G= (p.Arg749=)
c.2156G= (p.Arg719=)
c.2147G= (p.Arg716=)
3g.123291270C>GCA354223669ADCY5c.1847G>C (p.Arg616Pro)
c.2135G>C (p.Arg712Pro)
n.1573G>C
c.3245G>C (p.Arg1082Pro)
c.3170G>C (p.Arg1057Pro)
c.2120G>C (p.Arg707Pro)
c.2144G>C (p.Arg715Pro)
c.2195G>C (p.Arg732Pro)
c.1922G>C (p.Arg641Pro)
c.2246G>C (p.Arg749Pro)
c.2156G>C (p.Arg719Pro)
c.2147G>C (p.Arg716Pro)
3g.123291270C>TCA82904077ADCY5c.1847G>A (p.Arg616Gln)
c.2135G>A (p.Arg712Gln)
n.1573G>A
c.3245G>A (p.Arg1082Gln)
c.3170G>A (p.Arg1057Gln)
c.2120G>A (p.Arg707Gln)
c.2144G>A (p.Arg715Gln)
c.2195G>A (p.Arg732Gln)
c.1922G>A (p.Arg641Gln)
c.2246G>A (p.Arg749Gln)
c.2156G>A (p.Arg719Gln)
c.2147G>A (p.Arg716Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.123291271G>ACA2576836ADCY5c.1846C>T (p.Arg616Trp)
c.2134C>T (p.Arg712Trp)
n.1572C>T
c.3244C>T (p.Arg1082Trp)
c.3169C>T (p.Arg1057Trp)
c.2119C>T (p.Arg707Trp)
c.2143C>T (p.Arg715Trp)
c.2194C>T (p.Arg732Trp)
c.1921C>T (p.Arg641Trp)
c.2245C>T (p.Arg749Trp)
c.2155C>T (p.Arg719Trp)
c.2146C>T (p.Arg716Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.123291271G>CCA354223670ADCY5c.1846C>G (p.Arg616Gly)
c.2134C>G (p.Arg712Gly)
n.1572C>G
c.3244C>G (p.Arg1082Gly)
c.3169C>G (p.Arg1057Gly)
c.2119C>G (p.Arg707Gly)
c.2143C>G (p.Arg715Gly)
c.2194C>G (p.Arg732Gly)
c.1921C>G (p.Arg641Gly)
c.2245C>G (p.Arg749Gly)
c.2155C>G (p.Arg719Gly)
c.2146C>G (p.Arg716Gly)
3g.123291271G=CA1398330419ADCY5c.1846C= (p.Arg616=)
c.2134C= (p.Arg712=)
n.1572C=
c.3244C= (p.Arg1082=)
c.3169C= (p.Arg1057=)
c.2119C= (p.Arg707=)
c.2143C= (p.Arg715=)
c.2194C= (p.Arg732=)
c.1921C= (p.Arg641=)
c.2245C= (p.Arg749=)
c.2155C= (p.Arg719=)
c.2146C= (p.Arg716=)
3g.123291271G>TCA435431256ADCY5c.1846C>A (p.Arg616=)
c.2134C>A (p.Arg712=)
n.1572C>A
c.3244C>A (p.Arg1082=)
c.3169C>A (p.Arg1057=)
c.2119C>A (p.Arg707=)
c.2143C>A (p.Arg715=)
c.2194C>A (p.Arg732=)
c.1921C>A (p.Arg641=)
c.2245C>A (p.Arg749=)
c.2155C>A (p.Arg719=)
c.2146C>A (p.Arg716=)
gnomAD v4
3g.123291272C>ACA354223671ADCY5c.1845G>T (p.Glu615Asp)
c.2133G>T (p.Glu711Asp)
n.1571G>T
c.3243G>T (p.Glu1081Asp)
c.3168G>T (p.Glu1056Asp)
c.2118G>T (p.Glu706Asp)
c.2142G>T (p.Glu714Asp)
c.2193G>T (p.Glu731Asp)
c.1920G>T (p.Glu640Asp)
c.2244G>T (p.Glu748Asp)
c.2154G>T (p.Glu718Asp)
c.2145G>T (p.Glu715Asp)
gnomAD v4
3g.123291272C=CA1398330420ADCY5c.1845G= (p.Glu615=)
c.2133G= (p.Glu711=)
n.1571G=
c.3243G= (p.Glu1081=)
c.3168G= (p.Glu1056=)
c.2118G= (p.Glu706=)
c.2142G= (p.Glu714=)
c.2193G= (p.Glu731=)
c.1920G= (p.Glu640=)
c.2244G= (p.Glu748=)
c.2154G= (p.Glu718=)
c.2145G= (p.Glu715=)
3g.123291272C>GCA354223672ADCY5c.1845G>C (p.Glu615Asp)
c.2133G>C (p.Glu711Asp)
n.1571G>C
c.3243G>C (p.Glu1081Asp)
c.3168G>C (p.Glu1056Asp)
c.2118G>C (p.Glu706Asp)
c.2142G>C (p.Glu714Asp)
c.2193G>C (p.Glu731Asp)
c.1920G>C (p.Glu640Asp)
c.2244G>C (p.Glu748Asp)
c.2154G>C (p.Glu718Asp)
c.2145G>C (p.Glu715Asp)
3g.123291272C>TCA82904084ADCY5c.1845G>A (p.Glu615=)
c.2133G>A (p.Glu711=)
n.1571G>A
c.3243G>A (p.Glu1081=)
c.3168G>A (p.Glu1056=)
c.2118G>A (p.Glu706=)
c.2142G>A (p.Glu714=)
c.2193G>A (p.Glu731=)
c.1920G>A (p.Glu640=)
c.2244G>A (p.Glu748=)
c.2154G>A (p.Glu718=)
c.2145G>A (p.Glu715=)
dbSNP gnomAD v4
3g.123291273T>ACA354223673ADCY5c.1844A>T (p.Glu615Val)
c.2132A>T (p.Glu711Val)
n.1570A>T
c.3242A>T (p.Glu1081Val)
c.3167A>T (p.Glu1056Val)
c.2117A>T (p.Glu706Val)
c.2141A>T (p.Glu714Val)
c.2192A>T (p.Glu731Val)
c.1919A>T (p.Glu640Val)
c.2243A>T (p.Glu748Val)
c.2153A>T (p.Glu718Val)
c.2144A>T (p.Glu715Val)
3g.123291273T>CCA354223674ADCY5c.1844A>G (p.Glu615Gly)
c.2132A>G (p.Glu711Gly)
n.1570A>G
c.3242A>G (p.Glu1081Gly)
c.3167A>G (p.Glu1056Gly)
c.2117A>G (p.Glu706Gly)
c.2141A>G (p.Glu714Gly)
c.2192A>G (p.Glu731Gly)
c.1919A>G (p.Glu640Gly)
c.2243A>G (p.Glu748Gly)
c.2153A>G (p.Glu718Gly)
c.2144A>G (p.Glu715Gly)
3g.123291273T>GCA354223675ADCY5c.1844A>C (p.Glu615Ala)
c.2132A>C (p.Glu711Ala)
n.1570A>C
c.3242A>C (p.Glu1081Ala)
c.3167A>C (p.Glu1056Ala)
c.2117A>C (p.Glu706Ala)
c.2141A>C (p.Glu714Ala)
c.2192A>C (p.Glu731Ala)
c.1919A>C (p.Glu640Ala)
c.2243A>C (p.Glu748Ala)
c.2153A>C (p.Glu718Ala)
c.2144A>C (p.Glu715Ala)

Number of alleles fetched