Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47566732C>ACA412813413ARAFc.651C>A (p.Asn217Lys)
c.660C>A (p.Asn220Lys)
c.666C>A (p.Asn222Lys)
c.-7C>A (n.-7C>A)
 dbSNP COSMIC
Xg.47566732C=CA2427968733ARAFc.651C= (p.Asn217=)
c.660C= (p.Asn220=)
c.666C= (p.Asn222=)
c.-7C= (n.-7C=)
Xg.47566732C>GCA412813412ARAFc.651C>G (p.Asn217Lys)
c.660C>G (p.Asn220Lys)
c.666C>G (p.Asn222Lys)
c.-7C>G (n.-7C>G)
Xg.47566732C>TCA515989200ARAFc.651C>T (p.Asn217=)
c.660C>T (p.Asn220=)
c.666C>T (p.Asn222=)
c.-7C>T (n.-7C>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566733G>ACA412813414ARAFc.652G>A (p.Val218Ile)
c.661G>A (p.Val221Ile)
c.667G>A (p.Val223Ile)
c.-6G>A (n.-6G>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566733G>CCA412813416ARAFc.652G>C (p.Val218Leu)
c.661G>C (p.Val221Leu)
c.667G>C (p.Val223Leu)
c.-6G>C (n.-6G>C)
 dbSNP
Xg.47566733G=CA2427968734ARAFc.652G= (p.Val218=)
c.661G= (p.Val221=)
c.667G= (p.Val223=)
c.-6G= (n.-6G=)
Xg.47566733G>TCA412813415ARAFc.652G>T (p.Val218Phe)
c.661G>T (p.Val221Phe)
c.667G>T (p.Val223Phe)
c.-6G>T (n.-6G>T)
Xg.47566736_47566744delCA645603174ARAFc.655_663del (p.His219_Val221del)
c.664_672del (p.His222_Val224del)
c.670_678del (p.His224_Val226del)
c.-3_6del
 COSMIC
Xg.47566734T>ACA412813417ARAFc.653T>A (p.Val218Asp)
c.662T>A (p.Val221Asp)
c.668T>A (p.Val223Asp)
c.-5T>A (n.-5T>A)
Xg.47566734T>CCA412813418ARAFc.653T>C (p.Val218Ala)
c.662T>C (p.Val221Ala)
c.668T>C (p.Val223Ala)
c.-5T>C (n.-5T>C)
Xg.47566734T>GCA412813419ARAFc.653T>G (p.Val218Gly)
c.662T>G (p.Val221Gly)
c.668T>G (p.Val223Gly)
c.-5T>G (n.-5T>G)
Xg.47566735C>ACA515989204ARAFc.654C>A (p.Val218=)
c.663C>A (p.Val221=)
c.669C>A (p.Val223=)
c.-4C>A (n.-4C>A)
Xg.47566735C>GCA515989205ARAFc.654C>G (p.Val218=)
c.663C>G (p.Val221=)
c.669C>G (p.Val223=)
c.-4C>G (n.-4C>G)
 dbSNP
Xg.47566735C>TCA515989207ARAFc.654C>T (p.Val218=)
c.663C>T (p.Val221=)
c.669C>T (p.Val223=)
c.-4C>T (n.-4C>T)
Xg.47566736C>ACA412813420ARAFc.655C>A (p.His219Asn)
c.664C>A (p.His222Asn)
c.670C>A (p.His224Asn)
c.-3C>A (n.-3C>A)
 dbSNP
Xg.47566736C>GCA412813421ARAFc.655C>G (p.His219Asp)
c.664C>G (p.His222Asp)
c.670C>G (p.His224Asp)
c.-3C>G (n.-3C>G)
Xg.47566736C>TCA412813422ARAFc.655C>T (p.His219Tyr)
c.664C>T (p.His222Tyr)
c.670C>T (p.His224Tyr)
c.-3C>T (n.-3C>T)
Xg.47566737A=CA2427968735ARAFc.656A= (p.His219=)
c.665A= (p.His222=)
c.671A= (p.His224=)
c.-2A= (n.-2A=)
Xg.47566737A>CCA412813423ARAFc.656A>C (p.His219Pro)
c.665A>C (p.His222Pro)
c.671A>C (p.His224Pro)
c.-2A>C (n.-2A>C)
Xg.47566737A>GCA412813424ARAFc.656A>G (p.His219Arg)
c.665A>G (p.His222Arg)
c.671A>G (p.His224Arg)
c.-2A>G (n.-2A>G)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566737A>TCA412813426ARAFc.656A>T (p.His219Leu)
c.665A>T (p.His222Leu)
c.671A>T (p.His224Leu)
c.-2A>T (n.-2A>T)
Xg.47566738T>ACA412813427ARAFc.657T>A (p.His219Gln)
c.666T>A (p.His222Gln)
c.672T>A (p.His224Gln)
c.-1T>A (n.-1T>A)
Xg.47566738T>CCA515989212ARAFc.657T>C (p.His219=)
c.666T>C (p.His222=)
c.672T>C (p.His224=)
c.-1T>C (n.-1T>C)
Xg.47566738T>GCA412813428ARAFc.657T>G (p.His219Gln)
c.666T>G (p.His222Gln)
c.672T>G (p.His224Gln)
c.-1T>G (n.-1T>G)
Xg.47566739A>CCA412813432ARAFc.658A>C (p.Met220Leu)
c.667A>C (p.Met223Leu)
c.673A>C (p.Met225Leu)
c.1A>C (p.Met1Leu)
Xg.47566739A>GCA412813431ARAFc.658A>G (p.Met220Val)
c.667A>G (p.Met223Val)
c.673A>G (p.Met225Val)
c.1A>G (p.Met1Val)
 gnomAD v4
Xg.47566739A>TCA412813430ARAFc.658A>T (p.Met220Leu)
c.667A>T (p.Met223Leu)
c.673A>T (p.Met225Leu)
c.1A>T (p.Met1Leu)
Xg.47566740T>ACA412813433ARAFc.659T>A (p.Met220Lys)
c.668T>A (p.Met223Lys)
c.674T>A (p.Met225Lys)
c.2T>A (p.Met1Lys)
Xg.47566740T>CCA412813435ARAFc.659T>C (p.Met220Thr)
c.668T>C (p.Met223Thr)
c.674T>C (p.Met225Thr)
c.2T>C (p.Met1Thr)
Xg.47566740T>GCA412813437ARAFc.659T>G (p.Met220Arg)
c.668T>G (p.Met223Arg)
c.674T>G (p.Met225Arg)
c.2T>G (p.Met1Arg)
Xg.47566741G>ACA412813439ARAFc.660G>A (p.Met220Ile)
c.669G>A (p.Met223Ile)
c.675G>A (p.Met225Ile)
c.3G>A (p.Met1Ile)
Xg.47566741G>CCA412813440ARAFc.660G>C (p.Met220Ile)
c.669G>C (p.Met223Ile)
c.675G>C (p.Met225Ile)
c.3G>C (p.Met1Ile)
Xg.47566741G>TCA412813442ARAFc.660G>T (p.Met220Ile)
c.669G>T (p.Met223Ile)
c.675G>T (p.Met225Ile)
c.3G>T (p.Met1Ile)
Xg.47566742delCA2738526601ARAFc.661del (p.Val221SerfsTer?)
c.670del (p.Val224SerfsTer?)
c.676del (p.Val226SerfsTer?)
c.4del (p.Val2SerfsTer?)
 dbSNP
Xg.47566742G>ACA412813444ARAFc.661G>A (p.Val221Ile)
c.670G>A (p.Val224Ile)
c.676G>A (p.Val226Ile)
c.4G>A (p.Val2Ile)
Xg.47566742G>CCA412813446ARAFc.661G>C (p.Val221Leu)
c.670G>C (p.Val224Leu)
c.676G>C (p.Val226Leu)
c.4G>C (p.Val2Leu)
 dbSNP
Xg.47566742G>TCA412813447ARAFc.661G>T (p.Val221Phe)
c.670G>T (p.Val224Phe)
c.676G>T (p.Val226Phe)
c.4G>T (p.Val2Phe)
Xg.47566743T>ACA412813449ARAFc.662T>A (p.Val221Asp)
c.671T>A (p.Val224Asp)
c.677T>A (p.Val226Asp)
c.5T>A (p.Val2Asp)
 dbSNP
Xg.47566743T>CCA412813451ARAFc.662T>C (p.Val221Ala)
c.671T>C (p.Val224Ala)
c.677T>C (p.Val226Ala)
c.5T>C (p.Val2Ala)
Xg.47566743T>GCA412813452ARAFc.662T>G (p.Val221Gly)
c.671T>G (p.Val224Gly)
c.677T>G (p.Val226Gly)
c.5T>G (p.Val2Gly)
Xg.47566744C>ACA515989223ARAFc.663C>A (p.Val221=)
c.672C>A (p.Val224=)
c.678C>A (p.Val226=)
c.6C>A (p.Val2=)
 gnomAD v4
Xg.47566744C>GCA515989224ARAFc.663C>G (p.Val221=)
c.672C>G (p.Val224=)
c.678C>G (p.Val226=)
c.6C>G (p.Val2=)
Xg.47566744C>TCA515989222ARAFc.663C>T (p.Val221=)
c.672C>T (p.Val224=)
c.678C>T (p.Val226=)
c.6C>T (p.Val2=)
Xg.47566746_47566751dupCA2693580434ARAFc.665_670dup (p.Thr223_Thr224insSerThr)
c.674_679dup (p.Thr226_Thr227insSerThr)
c.680_685dup (p.Thr228_Thr229insSerThr)
c.8_13dup (p.Thr4_Thr5insSerThr)
 gnomAD v4
Xg.47566745A>CCA412813454ARAFc.664A>C (p.Ser222Arg)
c.673A>C (p.Ser225Arg)
c.679A>C (p.Ser227Arg)
c.7A>C (p.Ser3Arg)
Xg.47566745A>GCA412813457ARAFc.664A>G (p.Ser222Gly)
c.673A>G (p.Ser225Gly)
c.679A>G (p.Ser227Gly)
c.7A>G (p.Ser3Gly)
Xg.47566745A>TCA412813455ARAFc.664A>T (p.Ser222Cys)
c.673A>T (p.Ser225Cys)
c.679A>T (p.Ser227Cys)
c.7A>T (p.Ser3Cys)
Xg.47566746G>ACA10398057ARAFc.665G>A (p.Ser222Asn)
c.674G>A (p.Ser225Asn)
c.680G>A (p.Ser227Asn)
c.8G>A (p.Ser3Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566746G>CCA412813460ARAFc.665G>C (p.Ser222Thr)
c.674G>C (p.Ser225Thr)
c.680G>C (p.Ser227Thr)
c.8G>C (p.Ser3Thr)
Xg.47566746G=CA2427968736ARAFc.665G= (p.Ser222=)
c.674G= (p.Ser225=)
c.680G= (p.Ser227=)
c.8G= (p.Ser3=)
Xg.47566746G>TCA412813459ARAFc.665G>T (p.Ser222Ile)
c.674G>T (p.Ser225Ile)
c.680G>T (p.Ser227Ile)
c.8G>T (p.Ser3Ile)
 dbSNP
Xg.47566747C>ACA412813461ARAFc.666C>A (p.Ser222Arg)
c.675C>A (p.Ser225Arg)
c.681C>A (p.Ser227Arg)
c.9C>A (p.Ser3Arg)
Xg.47566747C>GCA412813462ARAFc.666C>G (p.Ser222Arg)
c.675C>G (p.Ser225Arg)
c.681C>G (p.Ser227Arg)
c.9C>G (p.Ser3Arg)
Xg.47566747C>TCA515989225ARAFc.666C>T (p.Ser222=)
c.675C>T (p.Ser225=)
c.681C>T (p.Ser227=)
c.9C>T (p.Ser3=)
 dbSNP
Xg.47566748A>CCA412813464ARAFc.667A>C (p.Thr223Pro)
c.676A>C (p.Thr226Pro)
c.682A>C (p.Thr228Pro)
c.10A>C (p.Thr4Pro)
Xg.47566748A>GCA412813465ARAFc.667A>G (p.Thr223Ala)
c.676A>G (p.Thr226Ala)
c.682A>G (p.Thr228Ala)
c.10A>G (p.Thr4Ala)
Xg.47566748A>TCA412813467ARAFc.667A>T (p.Thr223Ser)
c.676A>T (p.Thr226Ser)
c.682A>T (p.Thr228Ser)
c.10A>T (p.Thr4Ser)
Xg.47566749C>ACA412813469ARAFc.668C>A (p.Thr223Asn)
c.677C>A (p.Thr226Asn)
c.683C>A (p.Thr228Asn)
c.11C>A (p.Thr4Asn)
Xg.47566749C>GCA412813470ARAFc.668C>G (p.Thr223Ser)
c.677C>G (p.Thr226Ser)
c.683C>G (p.Thr228Ser)
c.11C>G (p.Thr4Ser)
Xg.47566749C>TCA412813472ARAFc.668C>T (p.Thr223Ile)
c.677C>T (p.Thr226Ile)
c.683C>T (p.Thr228Ile)
c.11C>T (p.Thr4Ile)
Xg.47566750C>ACA515989229ARAFc.669C>A (p.Thr223=)
c.678C>A (p.Thr226=)
c.684C>A (p.Thr228=)
c.12C>A (p.Thr4=)
 gnomAD v4
Xg.47566750C>GCA515989231ARAFc.669C>G (p.Thr223=)
c.678C>G (p.Thr226=)
c.684C>G (p.Thr228=)
c.12C>G (p.Thr4=)
Xg.47566750C>TCA515989230ARAFc.669C>T (p.Thr223=)
c.678C>T (p.Thr226=)
c.684C>T (p.Thr228=)
c.12C>T (p.Thr4=)
Xg.47566751A>CCA412813473ARAFc.670A>C (p.Thr224Pro)
c.679A>C (p.Thr227Pro)
c.685A>C (p.Thr229Pro)
c.13A>C (p.Thr5Pro)
 dbSNP
Xg.47566751A>GCA412813474ARAFc.670A>G (p.Thr224Ala)
c.679A>G (p.Thr227Ala)
c.685A>G (p.Thr229Ala)
c.13A>G (p.Thr5Ala)
Xg.47566751A>TCA412813476ARAFc.670A>T (p.Thr224Ser)
c.679A>T (p.Thr227Ser)
c.685A>T (p.Thr229Ser)
c.13A>T (p.Thr5Ser)
Xg.47566752C>ACA412813477ARAFc.671C>A (p.Thr224Lys)
c.680C>A (p.Thr227Lys)
c.686C>A (p.Thr229Lys)
c.14C>A (p.Thr5Lys)
Xg.47566752C>GCA412813479ARAFc.671C>G (p.Thr224Arg)
c.680C>G (p.Thr227Arg)
c.686C>G (p.Thr229Arg)
c.14C>G (p.Thr5Arg)
Xg.47566752C>TCA412813481ARAFc.671C>T (p.Thr224Met)
c.680C>T (p.Thr227Met)
c.686C>T (p.Thr229Met)
c.14C>T (p.Thr5Met)
 dbSNP gnomAD v4 COSMIC
Xg.47566753G>ACA10398058ARAFc.672G>A (p.Thr224=)
c.681G>A (p.Thr227=)
c.687G>A (p.Thr229=)
c.15G>A (p.Thr5=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566753G>CCA515989237ARAFc.672G>C (p.Thr224=)
c.681G>C (p.Thr227=)
c.687G>C (p.Thr229=)
c.15G>C (p.Thr5=)
Xg.47566753G=CA2427968737ARAFc.672G= (p.Thr224=)
c.681G= (p.Thr227=)
c.687G= (p.Thr229=)
c.15G= (p.Thr5=)
Xg.47566753G>TCA515989238ARAFc.672G>T (p.Thr224=)
c.681G>T (p.Thr227=)
c.687G>T (p.Thr229=)
c.15G>T (p.Thr5=)
 dbSNP
Xg.47566754G>ACA412813483ARAFc.673G>A (p.Ala225Thr)
c.682G>A (p.Ala228Thr)
c.688G>A (p.Ala230Thr)
c.16G>A (p.Ala6Thr)
 COSMIC
Xg.47566754G>CCA412813485ARAFc.673G>C (p.Ala225Pro)
c.682G>C (p.Ala228Pro)
c.688G>C (p.Ala230Pro)
c.16G>C (p.Ala6Pro)
Xg.47566754G=CA2427968738ARAFc.673G= (p.Ala225=)
c.682G= (p.Ala228=)
c.688G= (p.Ala230=)
c.16G= (p.Ala6=)
Xg.47566754G>TCA412813487ARAFc.673G>T (p.Ala225Ser)
c.682G>T (p.Ala228Ser)
c.688G>T (p.Ala230Ser)
c.16G>T (p.Ala6Ser)
 dbSNP
Xg.47566755C>ACA412813488ARAFc.674C>A (p.Ala225Asp)
c.683C>A (p.Ala228Asp)
c.689C>A (p.Ala230Asp)
c.17C>A (p.Ala6Asp)
 dbSNP gnomAD v4
Xg.47566755C=CA2427968739ARAFc.674C= (p.Ala225=)
c.683C= (p.Ala228=)
c.689C= (p.Ala230=)
c.17C= (p.Ala6=)
Xg.47566755C>GCA412813490ARAFc.674C>G (p.Ala225Gly)
c.683C>G (p.Ala228Gly)
c.689C>G (p.Ala230Gly)
c.17C>G (p.Ala6Gly)
Xg.47566755C>TCA412813492ARAFc.674C>T (p.Ala225Val)
c.683C>T (p.Ala228Val)
c.689C>T (p.Ala230Val)
c.17C>T (p.Ala6Val)
Xg.47566759delCA2693580435ARAFc.678del (p.Met227TrpfsTer?)
c.687del (p.Met230TrpfsTer?)
c.693del (p.Met232TrpfsTer?)
c.21del (p.Met8TrpfsTer?)
 gnomAD v4
Xg.47566756C>ACA515989239ARAFc.675C>A (p.Ala225=)
c.684C>A (p.Ala228=)
c.690C>A (p.Ala230=)
c.18C>A (p.Ala6=)
Xg.47566756C>GCA515989240ARAFc.675C>G (p.Ala225=)
c.684C>G (p.Ala228=)
c.690C>G (p.Ala230=)
c.18C>G (p.Ala6=)
Xg.47566756C>TCA515989241ARAFc.675C>T (p.Ala225=)
c.684C>T (p.Ala228=)
c.690C>T (p.Ala230=)
c.18C>T (p.Ala6=)
Xg.47566757C>ACA412813493ARAFc.676C>A (p.Pro226Thr)
c.685C>A (p.Pro229Thr)
c.691C>A (p.Pro231Thr)
c.19C>A (p.Pro7Thr)
 gnomAD v4
Xg.47566757C=CA2427968740ARAFc.676C= (p.Pro226=)
c.685C= (p.Pro229=)
c.691C= (p.Pro231=)
c.19C= (p.Pro7=)
Xg.47566757C>GCA412813495ARAFc.676C>G (p.Pro226Ala)
c.685C>G (p.Pro229Ala)
c.691C>G (p.Pro231Ala)
c.19C>G (p.Pro7Ala)
Xg.47566757C>TCA412813496ARAFc.676C>T (p.Pro226Ser)
c.685C>T (p.Pro229Ser)
c.691C>T (p.Pro231Ser)
c.19C>T (p.Pro7Ser)
 dbSNP gnomAD v4
Xg.47566758C>ACA412813498ARAFc.677C>A (p.Pro226His)
c.686C>A (p.Pro229His)
c.692C>A (p.Pro231His)
c.20C>A (p.Pro7His)
Xg.47566758C=CA2427968741ARAFc.677C= (p.Pro226=)
c.686C= (p.Pro229=)
c.692C= (p.Pro231=)
c.20C= (p.Pro7=)
Xg.47566758C>GCA412813500ARAFc.677C>G (p.Pro226Arg)
c.686C>G (p.Pro229Arg)
c.692C>G (p.Pro231Arg)
c.20C>G (p.Pro7Arg)
Xg.47566758C>TCA412813502ARAFc.677C>T (p.Pro226Leu)
c.686C>T (p.Pro229Leu)
c.692C>T (p.Pro231Leu)
c.20C>T (p.Pro7Leu)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566759C>ACA515989244ARAFc.678C>A (p.Pro226=)
c.687C>A (p.Pro229=)
c.693C>A (p.Pro231=)
c.21C>A (p.Pro7=)
Xg.47566759C>GCA515989245ARAFc.678C>G (p.Pro226=)
c.687C>G (p.Pro229=)
c.693C>G (p.Pro231=)
c.21C>G (p.Pro7=)
Xg.47566759C>TCA515989246ARAFc.678C>T (p.Pro226=)
c.687C>T (p.Pro229=)
c.693C>T (p.Pro231=)
c.21C>T (p.Pro7=)
Xg.47566760A=CA2427968742ARAFc.679A= (p.Met227=)
c.688A= (p.Met230=)
c.694A= (p.Met232=)
c.22A= (p.Met8=)
Xg.47566760A>CCA412813505ARAFc.679A>C (p.Met227Leu)
c.688A>C (p.Met230Leu)
c.694A>C (p.Met232Leu)
c.22A>C (p.Met8Leu)
Xg.47566760A>GCA10398059ARAFc.679A>G (p.Met227Val)
c.688A>G (p.Met230Val)
c.694A>G (p.Met232Val)
c.22A>G (p.Met8Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566760A>TCA412813503ARAFc.679A>T (p.Met227Leu)
c.688A>T (p.Met230Leu)
c.694A>T (p.Met232Leu)
c.22A>T (p.Met8Leu)
Xg.47566761T>ACA412813507ARAFc.680T>A (p.Met227Lys)
c.689T>A (p.Met230Lys)
c.695T>A (p.Met232Lys)
c.23T>A (p.Met8Lys)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566761T>CCA412813510ARAFc.680T>C (p.Met227Thr)
c.689T>C (p.Met230Thr)
c.695T>C (p.Met232Thr)
c.23T>C (p.Met8Thr)
Xg.47566761T>GCA412813512ARAFc.680T>G (p.Met227Arg)
c.689T>G (p.Met230Arg)
c.695T>G (p.Met232Arg)
c.23T>G (p.Met8Arg)
 gnomAD v4
Xg.47566761T=CA2427968743ARAFc.680T= (p.Met227=)
c.689T= (p.Met230=)
c.695T= (p.Met232=)
c.23T= (p.Met8=)
Xg.47566762G>ACA412813514ARAFc.681G>A (p.Met227Ile)
c.690G>A (p.Met230Ile)
c.696G>A (p.Met232Ile)
c.24G>A (p.Met8Ile)
 gnomAD v4
Xg.47566762G>CCA412813516ARAFc.681G>C (p.Met227Ile)
c.690G>C (p.Met230Ile)
c.696G>C (p.Met232Ile)
c.24G>C (p.Met8Ile)
Xg.47566762G>TCA412813517ARAFc.681G>T (p.Met227Ile)
c.690G>T (p.Met230Ile)
c.696G>T (p.Met232Ile)
c.24G>T (p.Met8Ile)
Xg.47566763G>ACA412813522ARAFc.682G>A (p.Asp228Asn)
c.691G>A (p.Asp231Asn)
c.697G>A (p.Asp233Asn)
c.25G>A (p.Asp9Asn)
 dbSNP
Xg.47566763G>CCA412813519ARAFc.682G>C (p.Asp228His)
c.691G>C (p.Asp231His)
c.697G>C (p.Asp233His)
c.25G>C (p.Asp9His)
 dbSNP
Xg.47566763G=CA2427968744ARAFc.682G= (p.Asp228=)
c.691G= (p.Asp231=)
c.697G= (p.Asp233=)
c.25G= (p.Asp9=)
Xg.47566763G>TCA412813520ARAFc.682G>T (p.Asp228Tyr)
c.691G>T (p.Asp231Tyr)
c.697G>T (p.Asp233Tyr)
c.25G>T (p.Asp9Tyr)
Xg.47566764A>CCA412813524ARAFc.683A>C (p.Asp228Ala)
c.692A>C (p.Asp231Ala)
c.698A>C (p.Asp233Ala)
c.26A>C (p.Asp9Ala)
Xg.47566764A>GCA412813526ARAFc.683A>G (p.Asp228Gly)
c.692A>G (p.Asp231Gly)
c.698A>G (p.Asp233Gly)
c.26A>G (p.Asp9Gly)
Xg.47566764A>TCA412813527ARAFc.683A>T (p.Asp228Val)
c.692A>T (p.Asp231Val)
c.698A>T (p.Asp233Val)
c.26A>T (p.Asp9Val)
 COSMIC
Xg.47566765C>ACA412813529ARAFc.684C>A (p.Asp228Glu)
c.693C>A (p.Asp231Glu)
c.699C>A (p.Asp233Glu)
c.27C>A (p.Asp9Glu)
Xg.47566765C>GCA412813530ARAFc.684C>G (p.Asp228Glu)
c.693C>G (p.Asp231Glu)
c.699C>G (p.Asp233Glu)
c.27C>G (p.Asp9Glu)
Xg.47566765C>TCA515989254ARAFc.684C>T (p.Asp228=)
c.693C>T (p.Asp231=)
c.699C>T (p.Asp233=)
c.27C>T (p.Asp9=)
Xg.47566766T>ACA412813532ARAFc.685T>A (p.Ser229Thr)
c.694T>A (p.Ser232Thr)
c.700T>A (p.Ser234Thr)
c.28T>A (p.Ser10Thr)
Xg.47566766T>CCA412813534ARAFc.685T>C (p.Ser229Pro)
c.694T>C (p.Ser232Pro)
c.700T>C (p.Ser234Pro)
c.28T>C (p.Ser10Pro)
Xg.47566766T>GCA412813533ARAFc.685T>G (p.Ser229Ala)
c.694T>G (p.Ser232Ala)
c.700T>G (p.Ser234Ala)
c.28T>G (p.Ser10Ala)
Xg.47566767C>ACA412813536ARAFc.686C>A (p.Ser229Tyr)
c.695C>A (p.Ser232Tyr)
c.701C>A (p.Ser234Tyr)
c.29C>A (p.Ser10Tyr)
Xg.47566767C>GCA412813537ARAFc.686C>G (p.Ser229Cys)
c.695C>G (p.Ser232Cys)
c.701C>G (p.Ser234Cys)
c.29C>G (p.Ser10Cys)
Xg.47566767C>TCA412813538ARAFc.686C>T (p.Ser229Phe)
c.695C>T (p.Ser232Phe)
c.701C>T (p.Ser234Phe)
c.29C>T (p.Ser10Phe)
 gnomAD v4
Xg.47566768C>ACA515989260ARAFc.687C>A (p.Ser229=)
c.696C>A (p.Ser232=)
c.702C>A (p.Ser234=)
c.30C>A (p.Ser10=)
Xg.47566768C>GCA515989261ARAFc.687C>G (p.Ser229=)
c.696C>G (p.Ser232=)
c.702C>G (p.Ser234=)
c.30C>G (p.Ser10=)
Xg.47566768C>TCA515989262ARAFc.687C>T (p.Ser229=)
c.696C>T (p.Ser232=)
c.702C>T (p.Ser234=)
c.30C>T (p.Ser10=)
Xg.47566769A>CCA412813539ARAFc.688A>C (p.Asn230His)
c.697A>C (p.Asn233His)
c.703A>C (p.Asn235His)
c.31A>C (p.Asn11His)
Xg.47566769A>GCA412813541ARAFc.688A>G (p.Asn230Asp)
c.697A>G (p.Asn233Asp)
c.703A>G (p.Asn235Asp)
c.31A>G (p.Asn11Asp)
Xg.47566769A>TCA412813542ARAFc.688A>T (p.Asn230Tyr)
c.697A>T (p.Asn233Tyr)
c.703A>T (p.Asn235Tyr)
c.31A>T (p.Asn11Tyr)
Xg.47566770A>CCA412813544ARAFc.689A>C (p.Asn230Thr)
c.698A>C (p.Asn233Thr)
c.704A>C (p.Asn235Thr)
c.32A>C (p.Asn11Thr)
Xg.47566770A>GCA412813546ARAFc.689A>G (p.Asn230Ser)
c.698A>G (p.Asn233Ser)
c.704A>G (p.Asn235Ser)
c.32A>G (p.Asn11Ser)
 gnomAD v4
Xg.47566770A>TCA412813547ARAFc.689A>T (p.Asn230Ile)
c.698A>T (p.Asn233Ile)
c.704A>T (p.Asn235Ile)
c.32A>T (p.Asn11Ile)
Xg.47566771C>ACA10398060ARAFc.690C>A (p.Asn230Lys)
c.699C>A (p.Asn233Lys)
c.705C>A (p.Asn235Lys)
c.33C>A (p.Asn11Lys)
 dbSNP ExAC gnomAD v2
Xg.47566771C=CA2427968745ARAFc.690C= (p.Asn230=)
c.699C= (p.Asn233=)
c.705C= (p.Asn235=)
c.33C= (p.Asn11=)
Xg.47566771C>GCA412813549ARAFc.690C>G (p.Asn230Lys)
c.699C>G (p.Asn233Lys)
c.705C>G (p.Asn235Lys)
c.33C>G (p.Asn11Lys)
Xg.47566771C>TCA515989267ARAFc.690C>T (p.Asn230=)
c.699C>T (p.Asn233=)
c.705C>T (p.Asn235=)
c.33C>T (p.Asn11=)
Xg.47566772C>ACA412813554ARAFc.691C>A (p.Leu231Ile)
c.700C>A (p.Leu234Ile)
c.706C>A (p.Leu236Ile)
c.34C>A (p.Leu12Ile)
 gnomAD v4
Xg.47566772C=CA2427968746ARAFc.691C= (p.Leu231=)
c.700C= (p.Leu234=)
c.706C= (p.Leu236=)
c.34C= (p.Leu12=)
Xg.47566772C>GCA412813553ARAFc.691C>G (p.Leu231Val)
c.700C>G (p.Leu234Val)
c.706C>G (p.Leu236Val)
c.34C>G (p.Leu12Val)
Xg.47566772C>TCA412813551ARAFc.691C>T (p.Leu231Phe)
c.700C>T (p.Leu234Phe)
c.706C>T (p.Leu236Phe)
c.34C>T (p.Leu12Phe)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566773T>ACA412813555ARAFc.692T>A (p.Leu231His)
c.701T>A (p.Leu234His)
c.707T>A (p.Leu236His)
c.35T>A (p.Leu12His)
 dbSNP
Xg.47566773T>CCA412813559ARAFc.692T>C (p.Leu231Pro)
c.701T>C (p.Leu234Pro)
c.707T>C (p.Leu236Pro)
c.35T>C (p.Leu12Pro)
Xg.47566773T>GCA412813557ARAFc.692T>G (p.Leu231Arg)
c.701T>G (p.Leu234Arg)
c.707T>G (p.Leu236Arg)
c.35T>G (p.Leu12Arg)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566773T=CA2427968747ARAFc.692T= (p.Leu231=)
c.701T= (p.Leu234=)
c.707T= (p.Leu236=)
c.35T= (p.Leu12=)
Xg.47566774C>ACA515989271ARAFc.693C>A (p.Leu231=)
c.702C>A (p.Leu234=)
c.708C>A (p.Leu236=)
c.36C>A (p.Leu12=)
 dbSNP
Xg.47566774C>GCA515989272ARAFc.693C>G (p.Leu231=)
c.702C>G (p.Leu234=)
c.708C>G (p.Leu236=)
c.36C>G (p.Leu12=)
Xg.47566774C>TCA515989273ARAFc.693C>T (p.Leu231=)
c.702C>T (p.Leu234=)
c.708C>T (p.Leu236=)
c.36C>T (p.Leu12=)
Xg.47566775A=CA2427968748ARAFc.694A= (p.Ile232=)
c.703A= (p.Ile235=)
c.709A= (p.Ile237=)
c.37A= (p.Ile13=)
Xg.47566775A>CCA412813561ARAFc.694A>C (p.Ile232Leu)
c.703A>C (p.Ile235Leu)
c.709A>C (p.Ile237Leu)
c.37A>C (p.Ile13Leu)
 dbSNP gnomAD v4
Xg.47566775A>GCA412813562ARAFc.694A>G (p.Ile232Val)
c.703A>G (p.Ile235Val)
c.709A>G (p.Ile237Val)
c.37A>G (p.Ile13Val)
 gnomAD v4
Xg.47566775A>TCA412813564ARAFc.694A>T (p.Ile232Phe)
c.703A>T (p.Ile235Phe)
c.709A>T (p.Ile237Phe)
c.37A>T (p.Ile13Phe)
 gnomAD v4
Xg.47566776T>ACA412813565ARAFc.695T>A (p.Ile232Asn)
c.704T>A (p.Ile235Asn)
c.710T>A (p.Ile237Asn)
c.38T>A (p.Ile13Asn)
Xg.47566776T>CCA412813566ARAFc.695T>C (p.Ile232Thr)
c.704T>C (p.Ile235Thr)
c.710T>C (p.Ile237Thr)
c.38T>C (p.Ile13Thr)
Xg.47566776T>GCA412813568ARAFc.695T>G (p.Ile232Ser)
c.704T>G (p.Ile235Ser)
c.710T>G (p.Ile237Ser)
c.38T>G (p.Ile13Ser)
Xg.47566777C>ACA515989275ARAFc.696C>A (p.Ile232=)
c.705C>A (p.Ile235=)
c.711C>A (p.Ile237=)
c.39C>A (p.Ile13=)
 COSMIC
Xg.47566777C=CA2427968749ARAFc.696C= (p.Ile232=)
c.705C= (p.Ile235=)
c.711C= (p.Ile237=)
c.39C= (p.Ile13=)
Xg.47566777C>GCA10398061ARAFc.696C>G (p.Ile232Met)
c.705C>G (p.Ile235Met)
c.711C>G (p.Ile237Met)
c.39C>G (p.Ile13Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566777C>TCA515989277ARAFc.696C>T (p.Ile232=)
c.705C>T (p.Ile235=)
c.711C>T (p.Ile237=)
c.39C>T (p.Ile13=)
 gnomAD v4
Xg.47566778C>ACA412813570ARAFc.697C>A (p.Gln233Lys)
c.706C>A (p.Gln236Lys)
c.712C>A (p.Gln238Lys)
c.40C>A (p.Gln14Lys)
Xg.47566778C>GCA412813572ARAFc.697C>G (p.Gln233Glu)
c.706C>G (p.Gln236Glu)
c.712C>G (p.Gln238Glu)
c.40C>G (p.Gln14Glu)
 dbSNP
Xg.47566778C>TCA412813573ARAFc.697C>T (p.Gln233Ter)
c.706C>T (p.Gln236Ter)
c.712C>T (p.Gln238Ter)
c.40C>T (p.Gln14Ter)
Xg.47566779A>CCA412813575ARAFc.698A>C (p.Gln233Pro)
c.707A>C (p.Gln236Pro)
c.713A>C (p.Gln238Pro)
c.41A>C (p.Gln14Pro)
Xg.47566779A>GCA412813576ARAFc.698A>G (p.Gln233Arg)
c.707A>G (p.Gln236Arg)
c.713A>G (p.Gln238Arg)
c.41A>G (p.Gln14Arg)
Xg.47566779A>TCA412813577ARAFc.698A>T (p.Gln233Leu)
c.707A>T (p.Gln236Leu)
c.713A>T (p.Gln238Leu)
c.41A>T (p.Gln14Leu)
Xg.47566780G>ACA515989280ARAFc.699G>A (p.Gln233=)
c.708G>A (p.Gln236=)
c.714G>A (p.Gln238=)
c.42G>A (p.Gln14=)
Xg.47566780G>CCA412813578ARAFc.699G>C (p.Gln233His)
c.708G>C (p.Gln236His)
c.714G>C (p.Gln238His)
c.42G>C (p.Gln14His)
Xg.47566780G>TCA412813580ARAFc.699G>T (p.Gln233His)
c.708G>T (p.Gln236His)
c.714G>T (p.Gln238His)
c.42G>T (p.Gln14His)
Xg.47566781G>ACA412813582ARAFc.699+1G>A (n.699+1G>A)
c.708+1G>A (n.708+1G>A)
c.714+1G>A (n.714+1G>A)
c.42+1G>A (n.42+1G>A)
Xg.47566781G>CCA412813583ARAFc.699+1G>C (n.699+1G>C)
c.708+1G>C (n.708+1G>C)
c.714+1G>C (n.714+1G>C)
c.42+1G>C (n.42+1G>C)
 dbSNP
Xg.47566781G>TCA412813584ARAFc.699+1G>T (n.699+1G>T)
c.708+1G>T (n.708+1G>T)
c.714+1G>T (n.714+1G>T)
c.42+1G>T (n.42+1G>T)
Xg.47566782T>ACA412813586ARAFc.699+2T>A (n.699+2T>A)
c.708+2T>A (n.708+2T>A)
c.714+2T>A (n.714+2T>A)
c.42+2T>A (n.42+2T>A)
Xg.47566782T>CCA412813588ARAFc.699+2T>C (n.699+2T>C)
c.708+2T>C (n.708+2T>C)
c.714+2T>C (n.714+2T>C)
c.42+2T>C (n.42+2T>C)
Xg.47566782T>GCA412813589ARAFc.699+2T>G (n.699+2T>G)
c.708+2T>G (n.708+2T>G)
c.714+2T>G (n.714+2T>G)
c.42+2T>G (n.42+2T>G)
Xg.47566784G>CCA329053225ARAFc.699+4G>C (n.699+4G>C)
c.708+4G>C (n.708+4G>C)
c.714+4G>C (n.714+4G>C)
c.42+4G>C (n.42+4G>C)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566784G=CA2427968750ARAFc.699+4G= (n.699+4G=)
c.708+4G= (n.708+4G=)
c.714+4G= (n.714+4G=)
c.42+4G= (n.42+4G=)
Xg.47566785G>ACA2738526844ARAFc.699+5G>A (n.699+5G>A)
c.708+5G>A (n.708+5G>A)
c.714+5G>A (n.714+5G>A)
c.42+5G>A (n.42+5G>A)
 dbSNP
Xg.47566787G>ACA2738363408ARAFc.699+7G>A (n.699+7G>A)
c.708+7G>A (n.708+7G>A)
c.714+7G>A (n.714+7G>A)
c.42+7G>A (n.42+7G>A)
 dbSNP
Xg.47566787G=CA2427968751ARAFc.699+7G= (n.699+7G=)
c.708+7G= (n.708+7G=)
c.714+7G= (n.714+7G=)
c.42+7G= (n.42+7G=)
Xg.47566787G>TCA10398062ARAFc.699+7G>T (n.699+7G>T)
c.708+7G>T (n.708+7G>T)
c.714+7G>T (n.714+7G>T)
c.42+7G>T (n.42+7G>T)
 dbSNP ExAC gnomAD v2
Xg.47566788C>ACA2693580436ARAFc.699+8C>A (n.699+8C>A)
c.708+8C>A (n.708+8C>A)
c.714+8C>A (n.714+8C>A)
c.42+8C>A (n.42+8C>A)
 gnomAD v4
Xg.47566788C>GCA2738526960ARAFc.699+8C>G (n.699+8C>G)
c.708+8C>G (n.708+8C>G)
c.714+8C>G (n.714+8C>G)
c.42+8C>G (n.42+8C>G)
 dbSNP
Xg.47566788C>TCA2738526990ARAFc.699+8C>T (n.699+8C>T)
c.708+8C>T (n.708+8C>T)
c.714+8C>T (n.714+8C>T)
c.42+8C>T (n.42+8C>T)
 dbSNP
Xg.47566789T>CCA10398063ARAFc.699+9T>C (n.699+9T>C)
c.708+9T>C (n.708+9T>C)
c.714+9T>C (n.714+9T>C)
c.42+9T>C (n.42+9T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566789T>GCA2693580437ARAFc.699+9T>G (n.699+9T>G)
c.708+9T>G (n.708+9T>G)
c.714+9T>G (n.714+9T>G)
c.42+9T>G (n.42+9T>G)
 gnomAD v4
Xg.47566789T=CA2427968752ARAFc.699+9T= (n.699+9T=)
c.708+9T= (n.708+9T=)
c.714+9T= (n.714+9T=)
c.42+9T= (n.42+9T=)
Xg.47566790G>ACA10398064ARAFc.699+10G>A (n.699+10G>A)
c.708+10G>A (n.708+10G>A)
c.714+10G>A (n.714+10G>A)
c.42+10G>A (n.42+10G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566790G=CA2427968753ARAFc.699+10G= (n.699+10G=)
c.708+10G= (n.708+10G=)
c.714+10G= (n.714+10G=)
c.42+10G= (n.42+10G=)
Xg.47566791T>GCA2738526995ARAFc.699+11T>G (n.699+11T>G)
c.708+11T>G (n.708+11T>G)
c.714+11T>G (n.714+11T>G)
c.42+11T>G (n.42+11T>G)
 dbSNP
Xg.47566792G>ACA2738526996ARAFc.699+12G>A (n.699+12G>A)
c.708+12G>A (n.708+12G>A)
c.714+12G>A (n.714+12G>A)
c.42+12G>A (n.42+12G>A)
 dbSNP
Xg.47566792G>CCA2693580438ARAFc.699+12G>C (n.699+12G>C)
c.708+12G>C (n.708+12G>C)
c.714+12G>C (n.714+12G>C)
c.42+12G>C (n.42+12G>C)
 dbSNP gnomAD v4
Xg.47566792G>TCA2738526997ARAFc.699+12G>T (n.699+12G>T)
c.708+12G>T (n.708+12G>T)
c.714+12G>T (n.714+12G>T)
c.42+12G>T (n.42+12G>T)
 dbSNP
Xg.47566796delCA2579596415ARAFc.699+16del (n.699+16del)
c.708+16del (n.708+16del)
c.714+16del (n.714+16del)
c.42+16del (n.42+16del)
Xg.47566793G>ACA2738527028ARAFc.699+13G>A (n.699+13G>A)
c.708+13G>A (n.708+13G>A)
c.714+13G>A (n.714+13G>A)
c.42+13G>A (n.42+13G>A)
 dbSNP
Xg.47566793G>TCA2738527010ARAFc.699+13G>T (n.699+13G>T)
c.708+13G>T (n.708+13G>T)
c.714+13G>T (n.714+13G>T)
c.42+13G>T (n.42+13G>T)
 dbSNP
Xg.47566794G>ACA2693580439ARAFc.699+14G>A (n.699+14G>A)
c.708+14G>A (n.708+14G>A)
c.714+14G>A (n.714+14G>A)
c.42+14G>A (n.42+14G>A)
 dbSNP gnomAD v4
Xg.47566794G>CCA2738527030ARAFc.699+14G>C (n.699+14G>C)
c.708+14G>C (n.708+14G>C)
c.714+14G>C (n.714+14G>C)
c.42+14G>C (n.42+14G>C)
 dbSNP
Xg.47566794G>TCA2738527031ARAFc.699+14G>T (n.699+14G>T)
c.708+14G>T (n.708+14G>T)
c.714+14G>T (n.714+14G>T)
c.42+14G>T (n.42+14G>T)
 dbSNP
Xg.47566795G>ACA2427968755ARAFc.699+15G>A (n.699+15G>A)
c.708+15G>A (n.708+15G>A)
c.714+15G>A (n.714+15G>A)
c.42+15G>A (n.42+15G>A)
 dbSNP gnomAD v4
Xg.47566795G=CA2427968754ARAFc.699+15G= (n.699+15G=)
c.708+15G= (n.708+15G=)
c.714+15G= (n.714+15G=)
c.42+15G= (n.42+15G=)
Xg.47566795G>TCA2693580440ARAFc.699+15G>T (n.699+15G>T)
c.708+15G>T (n.708+15G>T)
c.714+15G>T (n.714+15G>T)
c.42+15G>T (n.42+15G>T)
 dbSNP gnomAD v4
Xg.47566796G>ACA2693580441ARAFc.699+16G>A (n.699+16G>A)
c.708+16G>A (n.708+16G>A)
c.714+16G>A (n.714+16G>A)
c.42+16G>A (n.42+16G>A)
 gnomAD v4
Xg.47566796G>CCA2693580442ARAFc.699+16G>C (n.699+16G>C)
c.708+16G>C (n.708+16G>C)
c.714+16G>C (n.714+16G>C)
c.42+16G>C (n.42+16G>C)
 gnomAD v4
Xg.47566796G>TCA2693580443ARAFc.699+16G>T (n.699+16G>T)
c.708+16G>T (n.708+16G>T)
c.714+16G>T (n.714+16G>T)
c.42+16G>T (n.42+16G>T)
 gnomAD v4
Xg.47566797delCA2738527072ARAFc.699+17del (n.699+17del)
c.708+17del (n.708+17del)
c.714+17del (n.714+17del)
c.42+17del (n.42+17del)
 dbSNP
Xg.47566797A>GCA2738527059ARAFc.699+17A>G (n.699+17A>G)
c.708+17A>G (n.708+17A>G)
c.714+17A>G (n.714+17A>G)
c.42+17A>G (n.42+17A>G)
 dbSNP
Xg.47566797A>TCA2738527071ARAFc.699+17A>T (n.699+17A>T)
c.708+17A>T (n.708+17A>T)
c.714+17A>T (n.714+17A>T)
c.42+17A>T (n.42+17A>T)
 dbSNP
Xg.47566798C=CA2427968756ARAFc.699+18C= (n.699+18C=)
c.708+18C= (n.708+18C=)
c.714+18C= (n.714+18C=)
c.42+18C= (n.42+18C=)
Xg.47566798C>GCA2738363570ARAFc.699+18C>G (n.699+18C>G)
c.708+18C>G (n.708+18C>G)
c.714+18C>G (n.714+18C>G)
c.42+18C>G (n.42+18C>G)
 dbSNP
Xg.47566798C>TCA10398065ARAFc.699+18C>T (n.699+18C>T)
c.708+18C>T (n.708+18C>T)
c.714+18C>T (n.714+18C>T)
c.42+18C>T (n.42+18C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566800A>GCA2693580444ARAFc.699+20A>G (n.699+20A>G)
c.708+20A>G (n.708+20A>G)
c.714+20A>G (n.714+20A>G)
c.42+20A>G (n.42+20A>G)
 gnomAD v4
Xg.47566800A>TCA2738527089ARAFc.699+20A>T (n.699+20A>T)
c.708+20A>T (n.708+20A>T)
c.714+20A>T (n.714+20A>T)
c.42+20A>T (n.42+20A>T)
 dbSNP
Xg.47566801T>CCA2738527102ARAFc.699+21T>C (n.699+21T>C)
c.708+21T>C (n.708+21T>C)
c.714+21T>C (n.714+21T>C)
c.42+21T>C (n.42+21T>C)
 dbSNP
Xg.47566801T>GCA2738527101ARAFc.699+21T>G (n.699+21T>G)
c.708+21T>G (n.708+21T>G)
c.714+21T>G (n.714+21T>G)
c.42+21T>G (n.42+21T>G)
 dbSNP
Xg.47566803C>ACA2738527105ARAFc.699+23C>A (n.699+23C>A)
c.708+23C>A (n.708+23C>A)
c.714+23C>A (n.714+23C>A)
c.42+23C>A (n.42+23C>A)
 dbSNP
Xg.47566803C>GCA2738527171ARAFc.699+23C>G (n.699+23C>G)
c.708+23C>G (n.708+23C>G)
c.714+23C>G (n.714+23C>G)
c.42+23C>G (n.42+23C>G)
 dbSNP
Xg.47566803C>TCA2738527170ARAFc.699+23C>T (n.699+23C>T)
c.708+23C>T (n.708+23C>T)
c.714+23C>T (n.714+23C>T)
c.42+23C>T (n.42+23C>T)
 dbSNP
Xg.47566804C=CA2427968757ARAFc.699+24C= (n.699+24C=)
c.708+24C= (n.708+24C=)
c.714+24C= (n.714+24C=)
c.42+24C= (n.42+24C=)
Xg.47566804C>TCA10398066ARAFc.699+24C>T (n.699+24C>T)
c.708+24C>T (n.708+24C>T)
c.714+24C>T (n.714+24C>T)
c.42+24C>T (n.42+24C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566805G>ACA10398067ARAFc.699+25G>A (n.699+25G>A)
c.708+25G>A (n.708+25G>A)
c.714+25G>A (n.714+25G>A)
c.42+25G>A (n.42+25G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566805G>CCA2693580445ARAFc.699+25G>C (n.699+25G>C)
c.708+25G>C (n.708+25G>C)
c.714+25G>C (n.714+25G>C)
c.42+25G>C (n.42+25G>C)
 dbSNP gnomAD v4
Xg.47566805G=CA2427968758ARAFc.699+25G= (n.699+25G=)
c.708+25G= (n.708+25G=)
c.714+25G= (n.714+25G=)
c.42+25G= (n.42+25G=)
Xg.47566805G>TCA329053277ARAFc.699+25G>T (n.699+25G>T)
c.708+25G>T (n.708+25G>T)
c.714+25G>T (n.714+25G>T)
c.42+25G>T (n.42+25G>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566806G>ACA2427968760ARAFc.699+26G>A (n.699+26G>A)
c.708+26G>A (n.708+26G>A)
c.714+26G>A (n.714+26G>A)
c.42+26G>A (n.42+26G>A)
 dbSNP
Xg.47566806G>CCA2738386015ARAFc.699+26G>C (n.699+26G>C)
c.708+26G>C (n.708+26G>C)
c.714+26G>C (n.714+26G>C)
c.42+26G>C (n.42+26G>C)
 dbSNP
Xg.47566806G=CA2427968759ARAFc.699+26G= (n.699+26G=)
c.708+26G= (n.708+26G=)
c.714+26G= (n.714+26G=)
c.42+26G= (n.42+26G=)
Xg.47566806G>TCA2693580446ARAFc.699+26G>T (n.699+26G>T)
c.708+26G>T (n.708+26G>T)
c.714+26G>T (n.714+26G>T)
c.42+26G>T (n.42+26G>T)
 dbSNP gnomAD v4
Xg.47566807G>ACA10398068ARAFc.699+27G>A (n.699+27G>A)
c.708+27G>A (n.708+27G>A)
c.714+27G>A (n.714+27G>A)
c.42+27G>A (n.42+27G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566807G=CA2427968761ARAFc.699+27G= (n.699+27G=)
c.708+27G= (n.708+27G=)
c.714+27G= (n.714+27G=)
c.42+27G= (n.42+27G=)
Xg.47566808G>ACA2738362094ARAFc.699+28G>A (n.699+28G>A)
c.708+28G>A (n.708+28G>A)
c.714+28G>A (n.714+28G>A)
c.42+28G>A (n.42+28G>A)
 dbSNP
Xg.47566808G>CCA329053278ARAFc.699+28G>C (n.699+28G>C)
c.708+28G>C (n.708+28G>C)
c.714+28G>C (n.714+28G>C)
c.42+28G>C (n.42+28G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566808G=CA2427968762ARAFc.699+28G= (n.699+28G=)
c.708+28G= (n.708+28G=)
c.714+28G= (n.714+28G=)
c.42+28G= (n.42+28G=)
Xg.47566808G>TCA2738362093ARAFc.699+28G>T (n.699+28G>T)
c.708+28G>T (n.708+28G>T)
c.714+28G>T (n.714+28G>T)
c.42+28G>T (n.42+28G>T)
 dbSNP
Xg.47566809A=CA2427968763ARAFc.699+29A= (n.699+29A=)
c.708+29A= (n.708+29A=)
c.714+29A= (n.714+29A=)
c.42+29A= (n.42+29A=)
Xg.47566809A>GCA10398069ARAFc.699+29A>G (n.699+29A>G)
c.708+29A>G (n.708+29A>G)
c.714+29A>G (n.714+29A>G)
c.42+29A>G (n.42+29A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566809A>TCA2427968764ARAFc.699+29A>T (n.699+29A>T)
c.708+29A>T (n.708+29A>T)
c.714+29A>T (n.714+29A>T)
c.42+29A>T (n.42+29A>T)
 dbSNP
Xg.47566810C>ACA2738527187ARAFc.699+30C>A (n.699+30C>A)
c.708+30C>A (n.708+30C>A)
c.714+30C>A (n.714+30C>A)
c.42+30C>A (n.42+30C>A)
 dbSNP
Xg.47566810C>GCA2738527175ARAFc.699+30C>G (n.699+30C>G)
c.708+30C>G (n.708+30C>G)
c.714+30C>G (n.714+30C>G)
c.42+30C>G (n.42+30C>G)
 dbSNP
Xg.47566810C>TCA2693580447ARAFc.699+30C>T (n.699+30C>T)
c.708+30C>T (n.708+30C>T)
c.714+30C>T (n.714+30C>T)
c.42+30C>T (n.42+30C>T)
 dbSNP gnomAD v4
Xg.47566811C>ACA2738372240ARAFc.699+31C>A (n.699+31C>A)
c.708+31C>A (n.708+31C>A)
c.714+31C>A (n.714+31C>A)
c.42+31C>A (n.42+31C>A)
 dbSNP
Xg.47566811C=CA2427968765ARAFc.699+31C= (n.699+31C=)
c.708+31C= (n.708+31C=)
c.714+31C= (n.714+31C=)
c.42+31C= (n.42+31C=)
Xg.47566811C>TCA641900829ARAFc.699+31C>T (n.699+31C>T)
c.708+31C>T (n.708+31C>T)
c.714+31C>T (n.714+31C>T)
c.42+31C>T (n.42+31C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566812A=CA2427968766ARAFc.699+32A= (n.699+32A=)
c.708+32A= (n.708+32A=)
c.714+32A= (n.714+32A=)
c.42+32A= (n.42+32A=)
Xg.47566812A>GCA329053296ARAFc.699+32A>G (n.699+32A>G)
c.708+32A>G (n.708+32A>G)
c.714+32A>G (n.714+32A>G)
c.42+32A>G (n.42+32A>G)
 dbSNP
Xg.47566813C>ACA2738527211ARAFc.699+33C>A (n.699+33C>A)
c.708+33C>A (n.708+33C>A)
c.714+33C>A (n.714+33C>A)
c.42+33C>A (n.42+33C>A)
 dbSNP
Xg.47566813C>TCA2738527271ARAFc.699+33C>T (n.699+33C>T)
c.708+33C>T (n.708+33C>T)
c.714+33C>T (n.714+33C>T)
c.42+33C>T (n.42+33C>T)
 dbSNP
Xg.47566814A>GCA2693580448ARAFc.699+34A>G (n.699+34A>G)
c.708+34A>G (n.708+34A>G)
c.714+34A>G (n.714+34A>G)
c.42+34A>G (n.42+34A>G)
 gnomAD v4
Xg.47566814A>TCA2738527315ARAFc.699+34A>T (n.699+34A>T)
c.708+34A>T (n.708+34A>T)
c.714+34A>T (n.714+34A>T)
c.42+34A>T (n.42+34A>T)
 dbSNP
Xg.47566815G>ACA2738527317ARAFc.699+35G>A (n.699+35G>A)
c.708+35G>A (n.708+35G>A)
c.714+35G>A (n.714+35G>A)
c.42+35G>A (n.42+35G>A)
 dbSNP
Xg.47566815G>TCA2738527316ARAFc.699+35G>T (n.699+35G>T)
c.708+35G>T (n.708+35G>T)
c.714+35G>T (n.714+35G>T)
c.42+35G>T (n.42+35G>T)
 dbSNP
Xg.47566816G>ACA2738527319ARAFc.699+36G>A (n.699+36G>A)
c.708+36G>A (n.708+36G>A)
c.714+36G>A (n.714+36G>A)
c.42+36G>A (n.42+36G>A)
 dbSNP
Xg.47566817G>ACA2693580449ARAFc.699+37G>A (n.699+37G>A)
c.708+37G>A (n.708+37G>A)
c.714+37G>A (n.714+37G>A)
c.42+37G>A (n.42+37G>A)
 dbSNP gnomAD v4
Xg.47566818C>GCA2738527322ARAFc.699+38C>G (n.699+38C>G)
c.708+38C>G (n.708+38C>G)
c.714+38C>G (n.714+38C>G)
c.42+38C>G (n.42+38C>G)
 dbSNP
Xg.47566818C>TCA2738527363ARAFc.699+38C>T (n.699+38C>T)
c.708+38C>T (n.708+38C>T)
c.714+38C>T (n.714+38C>T)
c.42+38C>T (n.42+38C>T)
 dbSNP
Xg.47566820G>ACA2693580450ARAFc.699+40G>A (n.699+40G>A)
c.708+40G>A (n.708+40G>A)
c.714+40G>A (n.714+40G>A)
c.42+40G>A (n.42+40G>A)
 gnomAD v4
Xg.47566820G>CCA2693580451ARAFc.699+40G>C (n.699+40G>C)
c.708+40G>C (n.708+40G>C)
c.714+40G>C (n.714+40G>C)
c.42+40G>C (n.42+40G>C)
 dbSNP gnomAD v4
Xg.47566822G>ACA10398070ARAFc.699+42G>A (n.699+42G>A)
c.708+42G>A (n.708+42G>A)
c.714+42G>A (n.714+42G>A)
c.42+42G>A (n.42+42G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566822G=CA2427968767ARAFc.699+42G= (n.699+42G=)
c.708+42G= (n.708+42G=)
c.714+42G= (n.714+42G=)
c.42+42G= (n.42+42G=)
Xg.47566823G>ACA2738527391ARAFc.699+43G>A (n.699+43G>A)
c.708+43G>A (n.708+43G>A)
c.714+43G>A (n.714+43G>A)
c.42+43G>A (n.42+43G>A)
 dbSNP
Xg.47566823G>TCA2738527413ARAFc.699+43G>T (n.699+43G>T)
c.708+43G>T (n.708+43G>T)
c.714+43G>T (n.714+43G>T)
c.42+43G>T (n.42+43G>T)
 dbSNP
Xg.47566824G>ACA2738527418ARAFc.699+44G>A (n.699+44G>A)
c.708+44G>A (n.708+44G>A)
c.714+44G>A (n.714+44G>A)
c.42+44G>A (n.42+44G>A)
 dbSNP
Xg.47566825T>ACA2738386017ARAFc.699+45T>A (n.699+45T>A)
c.708+45T>A (n.708+45T>A)
c.714+45T>A (n.714+45T>A)
c.42+45T>A (n.42+45T>A)
 dbSNP
Xg.47566825T>CCA2738386016ARAFc.699+45T>C (n.699+45T>C)
c.708+45T>C (n.708+45T>C)
c.714+45T>C (n.714+45T>C)
c.42+45T>C (n.42+45T>C)
 dbSNP
Xg.47566825T>GCA1132891793ARAFc.699+45T>G (n.699+45T>G)
c.708+45T>G (n.708+45T>G)
c.714+45T>G (n.714+45T>G)
c.42+45T>G (n.42+45T>G)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566825T=CA2427968768ARAFc.699+45T= (n.699+45T=)
c.708+45T= (n.708+45T=)
c.714+45T= (n.714+45T=)
c.42+45T= (n.42+45T=)
Xg.47566826A=CA2427968769ARAFc.699+46A= (n.699+46A=)
c.708+46A= (n.708+46A=)
c.714+46A= (n.714+46A=)
c.42+46A= (n.42+46A=)
Xg.47566826A>CCA2693580452ARAFc.699+46A>C (n.699+46A>C)
c.708+46A>C (n.708+46A>C)
c.714+46A>C (n.714+46A>C)
c.42+46A>C (n.42+46A>C)
 gnomAD v4
Xg.47566826A>GCA329053301ARAFc.699+46A>G (n.699+46A>G)
c.708+46A>G (n.708+46A>G)
c.714+46A>G (n.714+46A>G)
c.42+46A>G (n.42+46A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566826A>TCA2738364918ARAFc.699+46A>T (n.699+46A>T)
c.708+46A>T (n.708+46A>T)
c.714+46A>T (n.714+46A>T)
c.42+46A>T (n.42+46A>T)
 dbSNP
Xg.47566827G>ACA2693580453ARAFc.699+47G>A (n.699+47G>A)
c.708+47G>A (n.708+47G>A)
c.714+47G>A (n.714+47G>A)
c.42+47G>A (n.42+47G>A)
 dbSNP gnomAD v4
Xg.47566828A>GCA2738527420ARAFc.699+48A>G (n.699+48A>G)
c.708+48A>G (n.708+48A>G)
c.714+48A>G (n.714+48A>G)
c.42+48A>G (n.42+48A>G)
 dbSNP
Xg.47566828A>TCA2738527422ARAFc.699+48A>T (n.699+48A>T)
c.708+48A>T (n.708+48A>T)
c.714+48A>T (n.714+48A>T)
c.42+48A>T (n.42+48A>T)
 dbSNP
Xg.47566829G>ACA2738527433ARAFc.699+49G>A (n.699+49G>A)
c.708+49G>A (n.708+49G>A)
c.714+49G>A (n.714+49G>A)
c.42+49G>A (n.42+49G>A)
 dbSNP
Xg.47566829G>CCA2579596416ARAFc.699+49G>C (n.699+49G>C)
c.708+49G>C (n.708+49G>C)
c.714+49G>C (n.714+49G>C)
c.42+49G>C (n.42+49G>C)
 dbSNP
Xg.47566829G>TCA2738527432ARAFc.699+49G>T (n.699+49G>T)
c.708+49G>T (n.708+49G>T)
c.714+49G>T (n.714+49G>T)
c.42+49G>T (n.42+49G>T)
 dbSNP
Xg.47566830C>ACA2738527463ARAFc.699+50C>A (n.699+50C>A)
c.708+50C>A (n.708+50C>A)
c.714+50C>A (n.714+50C>A)
c.42+50C>A (n.42+50C>A)
 dbSNP
Xg.47566830C>GCA2738527435ARAFc.699+50C>G (n.699+50C>G)
c.708+50C>G (n.708+50C>G)
c.714+50C>G (n.714+50C>G)
c.42+50C>G (n.42+50C>G)
 dbSNP
Xg.47566830C>TCA2738527484ARAFc.699+50C>T (n.699+50C>T)
c.708+50C>T (n.708+50C>T)
c.714+50C>T (n.714+50C>T)
c.42+50C>T (n.42+50C>T)
 dbSNP
Xg.47566831C>ACA2738527534ARAFc.699+51C>A (n.699+51C>A)
c.708+51C>A (n.708+51C>A)
c.714+51C>A (n.714+51C>A)
c.42+51C>A (n.42+51C>A)
 dbSNP
Xg.47566831C>TCA2738527526ARAFc.699+51C>T (n.699+51C>T)
c.708+51C>T (n.708+51C>T)
c.714+51C>T (n.714+51C>T)
c.42+51C>T (n.42+51C>T)
 dbSNP
Xg.47566832A=CA2427968771ARAFc.700-52A= (n.700-52A=)
c.709-52A= (n.709-52A=)
c.715-52A= (n.715-52A=)
c.43-52A= (n.43-52A=)
Xg.47566832A>CCA2738386019ARAFc.700-52A>C (n.700-52A>C)
c.709-52A>C (n.709-52A>C)
c.715-52A>C (n.715-52A>C)
c.43-52A>C (n.43-52A>C)
 dbSNP
Xg.47566832A>GCA2427968772ARAFc.700-52A>G (n.700-52A>G)
c.709-52A>G (n.709-52A>G)
c.715-52A>G (n.715-52A>G)
c.43-52A>G (n.43-52A>G)
 dbSNP
Xg.47566832A>TCA2738386018ARAFc.700-52A>T (n.700-52A>T)
c.709-52A>T (n.709-52A>T)
c.715-52A>T (n.715-52A>T)
c.43-52A>T (n.43-52A>T)
 dbSNP
Xg.47566832_47566837delinsATCCCTCA2427968770ARAFc.700-52_700-47delinsATCCCT (n.700-52_700-47delinsATCCCT)
c.709-52_709-47delinsATCCCT (n.709-52_709-47delinsATCCCT)
c.715-52_715-47delinsATCCCT (n.715-52_715-47delinsATCCCT)
c.43-52_43-47delinsATCCCT (n.43-52_43-47delinsATCCCT)

Number of alleles fetched