Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122284326C>ACA354159655CASRc.2141C>A (p.Ala714Asp)
c.2402C>A (p.Ala801Asp)
c.2372C>A (p.Ala791Asp)
c.1889C>A (p.Ala630Asp)
c.1784C>A (p.Ala595Asp)
COSMIC
3g.122284326C>GCA354159654CASRc.2141C>G (p.Ala714Gly)
c.2402C>G (p.Ala801Gly)
c.2372C>G (p.Ala791Gly)
c.1889C>G (p.Ala630Gly)
c.1784C>G (p.Ala595Gly)
3g.122284326C>TCA354159653CASRc.2141C>T (p.Ala714Val)
c.2402C>T (p.Ala801Val)
c.2372C>T (p.Ala791Val)
c.1889C>T (p.Ala630Val)
c.1784C>T (p.Ala595Val)
gnomAD v4
3g.122284327C>ACA435425145CASRc.2142C>A (p.Ala714=)
c.2403C>A (p.Ala801=)
c.2373C>A (p.Ala791=)
c.1890C>A (p.Ala630=)
c.1785C>A (p.Ala595=)
3g.122284327C=CA1397872190CASRc.2142C= (p.Ala714=)
c.2403C= (p.Ala801=)
c.2373C= (p.Ala791=)
c.1890C= (p.Ala630=)
c.1785C= (p.Ala595=)
3g.122284327C>GCA435425146CASRc.2142C>G (p.Ala714=)
c.2403C>G (p.Ala801=)
c.2373C>G (p.Ala791=)
c.1890C>G (p.Ala630=)
c.1785C>G (p.Ala595=)
3g.122284327C>TCA435425148CASRc.2142C>T (p.Ala714=)
c.2403C>T (p.Ala801=)
c.2373C>T (p.Ala791=)
c.1890C>T (p.Ala630=)
c.1785C>T (p.Ala595=)
ClinVar dbSNP
3g.122284328T>ACA354159656CASRc.2143T>A (p.Phe715Ile)
c.2404T>A (p.Phe802Ile)
c.2374T>A (p.Phe792Ile)
c.1891T>A (p.Phe631Ile)
c.1786T>A (p.Phe596Ile)
3g.122284328T>CCA354159657CASRc.2143T>C (p.Phe715Leu)
c.2404T>C (p.Phe802Leu)
c.2374T>C (p.Phe792Leu)
c.1891T>C (p.Phe631Leu)
c.1786T>C (p.Phe596Leu)
3g.122284328T>GCA354159658CASRc.2143T>G (p.Phe715Val)
c.2404T>G (p.Phe802Val)
c.2374T>G (p.Phe792Val)
c.1891T>G (p.Phe631Val)
c.1786T>G (p.Phe596Val)
3g.122284329T>ACA354159659CASRc.2144T>A (p.Phe715Tyr)
c.2405T>A (p.Phe802Tyr)
c.2375T>A (p.Phe792Tyr)
c.1892T>A (p.Phe631Tyr)
c.1787T>A (p.Phe596Tyr)
3g.122284329T>CCA354159660CASRc.2144T>C (p.Phe715Ser)
c.2405T>C (p.Phe802Ser)
c.2375T>C (p.Phe792Ser)
c.1892T>C (p.Phe631Ser)
c.1787T>C (p.Phe596Ser)
3g.122284329T>GCA354159661CASRc.2144T>G (p.Phe715Cys)
c.2405T>G (p.Phe802Cys)
c.2375T>G (p.Phe792Cys)
c.1892T>G (p.Phe631Cys)
c.1787T>G (p.Phe596Cys)
3g.122284330C>ACA354159662CASRc.2145C>A (p.Phe715Leu)
c.2406C>A (p.Phe802Leu)
c.2376C>A (p.Phe792Leu)
c.1893C>A (p.Phe631Leu)
c.1788C>A (p.Phe596Leu)
3g.122284330C=CA1397872196CASRc.2145C= (p.Phe715=)
c.2406C= (p.Phe802=)
c.2376C= (p.Phe792=)
c.1893C= (p.Phe631=)
c.1788C= (p.Phe596=)
3g.122284330C>GCA354159663CASRc.2145C>G (p.Phe715Leu)
c.2406C>G (p.Phe802Leu)
c.2376C>G (p.Phe792Leu)
c.1893C>G (p.Phe631Leu)
c.1788C>G (p.Phe596Leu)
3g.122284330C>TCA435425150CASRc.2145C>T (p.Phe715=)
c.2406C>T (p.Phe802=)
c.2376C>T (p.Phe792=)
c.1893C>T (p.Phe631=)
c.1788C>T (p.Phe596=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.122284331A>CCA354159664CASRc.2146A>C (p.Lys716Gln)
c.2407A>C (p.Lys803Gln)
c.2377A>C (p.Lys793Gln)
c.1894A>C (p.Lys632Gln)
c.1789A>C (p.Lys597Gln)
3g.122284331A>GCA354159665CASRc.2146A>G (p.Lys716Glu)
c.2407A>G (p.Lys803Glu)
c.2377A>G (p.Lys793Glu)
c.1894A>G (p.Lys632Glu)
c.1789A>G (p.Lys597Glu)
3g.122284331A>TCA354159666CASRc.2146A>T (p.Lys716Ter)
c.2407A>T (p.Lys803Ter)
c.2377A>T (p.Lys793Ter)
c.1894A>T (p.Lys632Ter)
c.1789A>T (p.Lys597Ter)
3g.122284332A>CCA354159669CASRc.2147A>C (p.Lys716Thr)
c.2408A>C (p.Lys803Thr)
c.2378A>C (p.Lys793Thr)
c.1895A>C (p.Lys632Thr)
c.1790A>C (p.Lys597Thr)
3g.122284332A>GCA354159668CASRc.2147A>G (p.Lys716Arg)
c.2408A>G (p.Lys803Arg)
c.2378A>G (p.Lys793Arg)
c.1895A>G (p.Lys632Arg)
c.1790A>G (p.Lys597Arg)
3g.122284332A>TCA354159667CASRc.2147A>T (p.Lys716Met)
c.2408A>T (p.Lys803Met)
c.2378A>T (p.Lys793Met)
c.1895A>T (p.Lys632Met)
c.1790A>T (p.Lys597Met)
ClinVar
3g.122284333G>ACA435425151CASRc.2148G>A (p.Lys716=)
c.2409G>A (p.Lys803=)
c.2379G>A (p.Lys793=)
c.1896G>A (p.Lys632=)
c.1791G>A (p.Lys597=)
ClinVar dbSNP
3g.122284333G>CCA354159670CASRc.2148G>C (p.Lys716Asn)
c.2409G>C (p.Lys803Asn)
c.2379G>C (p.Lys793Asn)
c.1896G>C (p.Lys632Asn)
c.1791G>C (p.Lys597Asn)
3g.122284333G>TCA354159671CASRc.2148G>T (p.Lys716Asn)
c.2409G>T (p.Lys803Asn)
c.2379G>T (p.Lys793Asn)
c.1896G>T (p.Lys632Asn)
c.1791G>T (p.Lys597Asn)
3g.122284334T>ACA354159672CASRc.2149T>A (p.Ser717Thr)
c.2410T>A (p.Ser804Thr)
c.2380T>A (p.Ser794Thr)
c.1897T>A (p.Ser633Thr)
c.1792T>A (p.Ser598Thr)
3g.122284334T>CCA354159673CASRc.2149T>C (p.Ser717Pro)
c.2410T>C (p.Ser804Pro)
c.2380T>C (p.Ser794Pro)
c.1897T>C (p.Ser633Pro)
c.1792T>C (p.Ser598Pro)
3g.122284334T>GCA354159674CASRc.2149T>G (p.Ser717Ala)
c.2410T>G (p.Ser804Ala)
c.2380T>G (p.Ser794Ala)
c.1897T>G (p.Ser633Ala)
c.1792T>G (p.Ser598Ala)
ClinVar
3g.122284335C>ACA354159675CASRc.2150C>A (p.Ser717Tyr)
c.2411C>A (p.Ser804Tyr)
c.2381C>A (p.Ser794Tyr)
c.1898C>A (p.Ser633Tyr)
c.1793C>A (p.Ser598Tyr)
3g.122284335C>GCA354159676CASRc.2150C>G (p.Ser717Cys)
c.2411C>G (p.Ser804Cys)
c.2381C>G (p.Ser794Cys)
c.1898C>G (p.Ser633Cys)
c.1793C>G (p.Ser598Cys)
3g.122284335C>TCA354159677CASRc.2150C>T (p.Ser717Phe)
c.2411C>T (p.Ser804Phe)
c.2381C>T (p.Ser794Phe)
c.1898C>T (p.Ser633Phe)
c.1793C>T (p.Ser598Phe)
gnomAD v4
3g.122284337delCA2580068645CASRc.2152del (p.Arg718GlyfsTer?)
c.2413del (p.Arg805GlyfsTer?)
c.2383del (p.Arg795GlyfsTer?)
c.1900del (p.Arg634GlyfsTer?)
c.1795del (p.Arg599GlyfsTer?)
ClinVar dbSNP
3g.122284336C>ACA435425153CASRc.2151C>A (p.Ser717=)
c.2412C>A (p.Ser804=)
c.2382C>A (p.Ser794=)
c.1899C>A (p.Ser633=)
c.1794C>A (p.Ser598=)
3g.122284336C>GCA435425154CASRc.2151C>G (p.Ser717=)
c.2412C>G (p.Ser804=)
c.2382C>G (p.Ser794=)
c.1899C>G (p.Ser633=)
c.1794C>G (p.Ser598=)
3g.122284336C>TCA435425156CASRc.2151C>T (p.Ser717=)
c.2412C>T (p.Ser804=)
c.2382C>T (p.Ser794=)
c.1899C>T (p.Ser633=)
c.1794C>T (p.Ser598=)
ClinVar
3g.122284337C>ACA435425159CASRc.2152C>A (p.Arg718=)
c.2413C>A (p.Arg805=)
c.2383C>A (p.Arg795=)
c.1900C>A (p.Arg634=)
c.1795C>A (p.Arg599=)
gnomAD v4
3g.122284337C=CA1397872200CASRc.2152C= (p.Arg718=)
c.2413C= (p.Arg805=)
c.2383C= (p.Arg795=)
c.1900C= (p.Arg634=)
c.1795C= (p.Arg599=)
3g.122284337C>GCA354159678CASRc.2152C>G (p.Arg718Gly)
c.2413C>G (p.Arg805Gly)
c.2383C>G (p.Arg795Gly)
c.1900C>G (p.Arg634Gly)
c.1795C>G (p.Arg599Gly)
ClinVar dbSNP
3g.122284337C>TCA119467CASRc.2152C>T (p.Arg718Trp)
c.2413C>T (p.Arg805Trp)
c.2383C>T (p.Arg795Trp)
c.1900C>T (p.Arg634Trp)
c.1795C>T (p.Arg599Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.122284338G>ACA82748943CASRc.2153G>A (p.Arg718Gln)
c.2414G>A (p.Arg805Gln)
c.2384G>A (p.Arg795Gln)
c.1901G>A (p.Arg634Gln)
c.1796G>A (p.Arg599Gln)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.122284338G>CCA354159679CASRc.2153G>C (p.Arg718Pro)
c.2414G>C (p.Arg805Pro)
c.2384G>C (p.Arg795Pro)
c.1901G>C (p.Arg634Pro)
c.1796G>C (p.Arg599Pro)
ClinVar
3g.122284338G=CA1397872205CASRc.2153G= (p.Arg718=)
c.2414G= (p.Arg805=)
c.2384G= (p.Arg795=)
c.1901G= (p.Arg634=)
c.1796G= (p.Arg599=)
3g.122284338G>TCA354159680CASRc.2153G>T (p.Arg718Leu)
c.2414G>T (p.Arg805Leu)
c.2384G>T (p.Arg795Leu)
c.1901G>T (p.Arg634Leu)
c.1796G>T (p.Arg599Leu)
ClinVar dbSNP
3g.122284339G>ACA435425160CASRc.2154G>A (p.Arg718=)
c.2415G>A (p.Arg805=)
c.2385G>A (p.Arg795=)
c.1902G>A (p.Arg634=)
c.1797G>A (p.Arg599=)
dbSNP
3g.122284339G>CCA435425161CASRc.2154G>C (p.Arg718=)
c.2415G>C (p.Arg805=)
c.2385G>C (p.Arg795=)
c.1902G>C (p.Arg634=)
c.1797G>C (p.Arg599=)
3g.122284339G=CA1397872209CASRc.2154G= (p.Arg718=)
c.2415G= (p.Arg805=)
c.2385G= (p.Arg795=)
c.1902G= (p.Arg634=)
c.1797G= (p.Arg599=)
3g.122284339G>TCA435425163CASRc.2154G>T (p.Arg718=)
c.2415G>T (p.Arg805=)
c.2385G>T (p.Arg795=)
c.1902G>T (p.Arg634=)
c.1797G>T (p.Arg599=)
3g.122284340A>CCA354159682CASRc.2155A>C (p.Lys719Gln)
c.2416A>C (p.Lys806Gln)
c.2386A>C (p.Lys796Gln)
c.1903A>C (p.Lys635Gln)
c.1798A>C (p.Lys600Gln)
3g.122284340A>GCA354159683CASRc.2155A>G (p.Lys719Glu)
c.2416A>G (p.Lys806Glu)
c.2386A>G (p.Lys796Glu)
c.1903A>G (p.Lys635Glu)
c.1798A>G (p.Lys600Glu)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched