Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122284595T>ACA354160468CASRc.2410T>A (p.Phe804Ile)
c.2671T>A (p.Phe891Ile)
c.2641T>A (p.Phe881Ile)
c.2158T>A (p.Phe720Ile)
c.2053T>A (p.Phe685Ile)
3g.122284595T>CCA119515CASRc.2410T>C (p.Phe804Leu)
c.2671T>C (p.Phe891Leu)
c.2641T>C (p.Phe881Leu)
c.2158T>C (p.Phe720Leu)
c.2053T>C (p.Phe685Leu)
ClinVar dbSNP
3g.122284595T>GCA354160469CASRc.2410T>G (p.Phe804Val)
c.2671T>G (p.Phe891Val)
c.2641T>G (p.Phe881Val)
c.2158T>G (p.Phe720Val)
c.2053T>G (p.Phe685Val)
3g.122284595T=CA1397872698CASRc.2410T= (p.Phe804=)
c.2671T= (p.Phe891=)
c.2641T= (p.Phe881=)
c.2158T= (p.Phe720=)
c.2053T= (p.Phe685=)
3g.122284596T>ACA354160472CASRc.2411T>A (p.Phe804Tyr)
c.2672T>A (p.Phe891Tyr)
c.2642T>A (p.Phe881Tyr)
c.2159T>A (p.Phe720Tyr)
c.2054T>A (p.Phe685Tyr)
3g.122284596T>CCA354160470CASRc.2411T>C (p.Phe804Ser)
c.2672T>C (p.Phe891Ser)
c.2642T>C (p.Phe881Ser)
c.2159T>C (p.Phe720Ser)
c.2054T>C (p.Phe685Ser)
3g.122284596T>GCA354160471CASRc.2411T>G (p.Phe804Cys)
c.2672T>G (p.Phe891Cys)
c.2642T>G (p.Phe881Cys)
c.2159T>G (p.Phe720Cys)
c.2054T>G (p.Phe685Cys)
3g.122284597C>ACA354160473CASRc.2412C>A (p.Phe804Leu)
c.2673C>A (p.Phe891Leu)
c.2643C>A (p.Phe881Leu)
c.2160C>A (p.Phe720Leu)
c.2055C>A (p.Phe685Leu)
3g.122284597C>GCA354160474CASRc.2412C>G (p.Phe804Leu)
c.2673C>G (p.Phe891Leu)
c.2643C>G (p.Phe881Leu)
c.2160C>G (p.Phe720Leu)
c.2055C>G (p.Phe685Leu)
3g.122284597C>TCA435425412CASRc.2412C>T (p.Phe804=)
c.2673C>T (p.Phe891=)
c.2643C>T (p.Phe881=)
c.2160C>T (p.Phe720=)
c.2055C>T (p.Phe685=)
COSMIC
3g.122284598A=CA1397872701CASRc.2413A= (p.Lys805=)
c.2674A= (p.Lys892=)
c.2644A= (p.Lys882=)
c.2161A= (p.Lys721=)
c.2056A= (p.Lys686=)
3g.122284598A>CCA354160475CASRc.2413A>C (p.Lys805Gln)
c.2674A>C (p.Lys892Gln)
c.2644A>C (p.Lys882Gln)
c.2161A>C (p.Lys721Gln)
c.2056A>C (p.Lys686Gln)
3g.122284598A>GCA354160476CASRc.2413A>G (p.Lys805Glu)
c.2674A>G (p.Lys892Glu)
c.2644A>G (p.Lys882Glu)
c.2161A>G (p.Lys721Glu)
c.2056A>G (p.Lys686Glu)
3g.122284598A>TCA213590CASRc.2413A>T (p.Lys805Ter)
c.2674A>T (p.Lys892Ter)
c.2644A>T (p.Lys882Ter)
c.2161A>T (p.Lys721Ter)
c.2056A>T (p.Lys686Ter)
ClinVar dbSNP
3g.122284599A=CA1397872708CASRc.2414A= (p.Lys805=)
c.2675A= (p.Lys892=)
c.2645A= (p.Lys882=)
c.2162A= (p.Lys721=)
c.2057A= (p.Lys686=)
3g.122284599A>CCA354160477CASRc.2414A>C (p.Lys805Thr)
c.2675A>C (p.Lys892Thr)
c.2645A>C (p.Lys882Thr)
c.2162A>C (p.Lys721Thr)
c.2057A>C (p.Lys686Thr)
3g.122284599A>GCA354160479CASRc.2414A>G (p.Lys805Arg)
c.2675A>G (p.Lys892Arg)
c.2645A>G (p.Lys882Arg)
c.2162A>G (p.Lys721Arg)
c.2057A>G (p.Lys686Arg)
ClinVar dbSNP
3g.122284599A>TCA354160478CASRc.2414A>T (p.Lys805Met)
c.2675A>T (p.Lys892Met)
c.2645A>T (p.Lys882Met)
c.2162A>T (p.Lys721Met)
c.2057A>T (p.Lys686Met)
3g.122284600G>ACA435425414CASRc.2415G>A (p.Lys805=)
c.2676G>A (p.Lys892=)
c.2646G>A (p.Lys882=)
c.2163G>A (p.Lys721=)
c.2058G>A (p.Lys686=)
3g.122284600G>CCA354160480CASRc.2415G>C (p.Lys805Asn)
c.2676G>C (p.Lys892Asn)
c.2646G>C (p.Lys882Asn)
c.2163G>C (p.Lys721Asn)
c.2058G>C (p.Lys686Asn)
3g.122284600G=CA1397872711CASRc.2415G= (p.Lys805=)
c.2676G= (p.Lys892=)
c.2646G= (p.Lys882=)
c.2163G= (p.Lys721=)
c.2058G= (p.Lys686=)
3g.122284600G>TCA354160481CASRc.2415G>T (p.Lys805Asn)
c.2676G>T (p.Lys892Asn)
c.2646G>T (p.Lys882Asn)
c.2163G>T (p.Lys721Asn)
c.2058G>T (p.Lys686Asn)
dbSNP gnomAD v3 gnomAD v4
3g.122284601G>ACA354160482CASRc.2416G>A (p.Val806Met)
c.2677G>A (p.Val893Met)
c.2647G>A (p.Val883Met)
c.2164G>A (p.Val722Met)
c.2059G>A (p.Val687Met)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.122284601G>CCA354160483CASRc.2416G>C (p.Val806Leu)
c.2677G>C (p.Val893Leu)
c.2647G>C (p.Val883Leu)
c.2164G>C (p.Val722Leu)
c.2059G>C (p.Val687Leu)
3g.122284601G=CA1397872713CASRc.2416G= (p.Val806=)
c.2677G= (p.Val893=)
c.2647G= (p.Val883=)
c.2164G= (p.Val722=)
c.2059G= (p.Val687=)
3g.122284601G>TCA354160484CASRc.2416G>T (p.Val806Leu)
c.2677G>T (p.Val893Leu)
c.2647G>T (p.Val883Leu)
c.2164G>T (p.Val722Leu)
c.2059G>T (p.Val687Leu)
3g.122284602T>ACA354160485CASRc.2417T>A (p.Val806Glu)
c.2678T>A (p.Val893Glu)
c.2648T>A (p.Val883Glu)
c.2165T>A (p.Val722Glu)
c.2060T>A (p.Val687Glu)
3g.122284602T>CCA354160486CASRc.2417T>C (p.Val806Ala)
c.2678T>C (p.Val893Ala)
c.2648T>C (p.Val883Ala)
c.2165T>C (p.Val722Ala)
c.2060T>C (p.Val687Ala)
3g.122284602T>GCA354160487CASRc.2417T>G (p.Val806Gly)
c.2678T>G (p.Val893Gly)
c.2648T>G (p.Val883Gly)
c.2165T>G (p.Val722Gly)
c.2060T>G (p.Val687Gly)
dbSNP
3g.122284602T=CA1397872715CASRc.2417T= (p.Val806=)
c.2678T= (p.Val893=)
c.2648T= (p.Val883=)
c.2165T= (p.Val722=)
c.2060T= (p.Val687=)
3g.122284604_122284607dupCA2667224704CASRc.2419_2422dup (p.Ala808GlyfsTer?)
c.2680_2683dup (p.Ala895GlyfsTer?)
c.2650_2653dup (p.Ala885GlyfsTer?)
c.2167_2170dup (p.Ala724GlyfsTer?)
c.2062_2065dup (p.Ala689GlyfsTer?)
gnomAD v4
3g.122284603G>ACA435425416CASRc.2418G>A (p.Val806=)
c.2679G>A (p.Val893=)
c.2649G>A (p.Val883=)
c.2166G>A (p.Val722=)
c.2061G>A (p.Val687=)
3g.122284603G>CCA435425417CASRc.2418G>C (p.Val806=)
c.2679G>C (p.Val893=)
c.2649G>C (p.Val883=)
c.2166G>C (p.Val722=)
c.2061G>C (p.Val687=)
3g.122284603G>TCA435425418CASRc.2418G>T (p.Val806=)
c.2679G>T (p.Val893=)
c.2649G>T (p.Val883=)
c.2166G>T (p.Val722=)
c.2061G>T (p.Val687=)
3g.122284604G>ACA354160488CASRc.2419G>A (p.Ala807Thr)
c.2680G>A (p.Ala894Thr)
c.2650G>A (p.Ala884Thr)
c.2167G>A (p.Ala723Thr)
c.2062G>A (p.Ala688Thr)
3g.122284604G>CCA354160489CASRc.2419G>C (p.Ala807Pro)
c.2680G>C (p.Ala894Pro)
c.2650G>C (p.Ala884Pro)
c.2167G>C (p.Ala723Pro)
c.2062G>C (p.Ala688Pro)
3g.122284604G>TCA354160490CASRc.2419G>T (p.Ala807Ser)
c.2680G>T (p.Ala894Ser)
c.2650G>T (p.Ala884Ser)
c.2167G>T (p.Ala723Ser)
c.2062G>T (p.Ala688Ser)
COSMIC
3g.122284605delCA2580068665CASRc.2420del (p.Ala807ValfsTer?)
c.2681del (p.Ala894ValfsTer?)
c.2651del (p.Ala884ValfsTer?)
c.2168del (p.Ala723ValfsTer?)
c.2063del (p.Ala688ValfsTer?)
ClinVar
3g.122284605C>ACA354160493CASRc.2420C>A (p.Ala807Asp)
c.2681C>A (p.Ala894Asp)
c.2651C>A (p.Ala884Asp)
c.2168C>A (p.Ala723Asp)
c.2063C>A (p.Ala688Asp)
3g.122284605C>GCA354160492CASRc.2420C>G (p.Ala807Gly)
c.2681C>G (p.Ala894Gly)
c.2651C>G (p.Ala884Gly)
c.2168C>G (p.Ala723Gly)
c.2063C>G (p.Ala688Gly)
3g.122284605C>TCA354160491CASRc.2420C>T (p.Ala807Val)
c.2681C>T (p.Ala894Val)
c.2651C>T (p.Ala884Val)
c.2168C>T (p.Ala723Val)
c.2063C>T (p.Ala688Val)
COSMIC
3g.122284606T>ACA435425421CASRc.2421T>A (p.Ala807=)
c.2682T>A (p.Ala894=)
c.2652T>A (p.Ala884=)
c.2169T>A (p.Ala723=)
c.2064T>A (p.Ala688=)
3g.122284606T>CCA435425422CASRc.2421T>C (p.Ala807=)
c.2682T>C (p.Ala894=)
c.2652T>C (p.Ala884=)
c.2169T>C (p.Ala723=)
c.2064T>C (p.Ala688=)
dbSNP gnomAD v2 gnomAD v4
3g.122284606T>GCA435425423CASRc.2421T>G (p.Ala807=)
c.2682T>G (p.Ala894=)
c.2652T>G (p.Ala884=)
c.2169T>G (p.Ala723=)
c.2064T>G (p.Ala688=)
dbSNP gnomAD v4
3g.122284606T=CA1397872718CASRc.2421T= (p.Ala807=)
c.2682T= (p.Ala894=)
c.2652T= (p.Ala884=)
c.2169T= (p.Ala723=)
c.2064T= (p.Ala688=)
3g.122284607G>ACA354160496CASRc.2422G>A (p.Ala808Thr)
c.2683G>A (p.Ala895Thr)
c.2653G>A (p.Ala885Thr)
c.2170G>A (p.Ala724Thr)
c.2065G>A (p.Ala689Thr)
3g.122284607G>CCA354160494CASRc.2422G>C (p.Ala808Pro)
c.2683G>C (p.Ala895Pro)
c.2653G>C (p.Ala885Pro)
c.2170G>C (p.Ala724Pro)
c.2065G>C (p.Ala689Pro)
3g.122284607G>TCA354160495CASRc.2422G>T (p.Ala808Ser)
c.2683G>T (p.Ala895Ser)
c.2653G>T (p.Ala885Ser)
c.2170G>T (p.Ala724Ser)
c.2065G>T (p.Ala689Ser)
gnomAD v4
3g.122284607_122284636delCA2580068666CASRc.2422_2451del (p.Ala808_Val817del)
c.2683_2712del (p.Ala895_Val904del)
c.2653_2682del (p.Ala885_Val894del)
c.2170_2199del (p.Ala724_Val733del)
c.2065_2094del (p.Ala689_Val698del)
ClinVar dbSNP
3g.122284608C>ACA354160497CASRc.2423C>A (p.Ala808Asp)
c.2684C>A (p.Ala895Asp)
c.2654C>A (p.Ala885Asp)
c.2171C>A (p.Ala724Asp)
c.2066C>A (p.Ala689Asp)

Number of alleles fetched