Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.151674498T>ACA429243035NEBc.3966A>T (p.Ala1322=)
2g.151674498T>CCA429243036NEBc.3966A>G (p.Ala1322=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.151674498T>GCA429243037NEBc.3966A>C (p.Ala1322=)
2g.151674498T=CA1298292925NEBc.3966A= (p.Ala1322=)
2g.151674499G>ACA348817660NEBc.3965C>T (p.Ala1322Val)
2g.151674499G>CCA348817661NEBc.3965C>G (p.Ala1322Gly)
2g.151674499G>TCA348817662NEBc.3965C>A (p.Ala1322Glu)
2g.151674500C>ACA1910778NEBc.3964G>T (p.Ala1322Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.151674500C=CA1298292930NEBc.3964G= (p.Ala1322=)
2g.151674500C>GCA348817663NEBc.3964G>C (p.Ala1322Pro)
2g.151674500C>TCA348817664NEBc.3964G>A (p.Ala1322Thr)
2g.151674501C>ACA348817666NEBc.3963G>T (p.Lys1321Asn)
2g.151674501C>GCA348817665NEBc.3963G>C (p.Lys1321Asn)
2g.151674501C>TCA429243039NEBc.3963G>A (p.Lys1321=)
2g.151674502T>ACA348817667NEBc.3962A>T (p.Lys1321Met)
2g.151674502T>CCA1910779NEBc.3962A>G (p.Lys1321Arg)
dbSNP ExAC
2g.151674502T>GCA348817668NEBc.3962A>C (p.Lys1321Thr)
2g.151674502T=CA1298292937NEBc.3962A= (p.Lys1321=)
2g.151674503T>ACA348817669NEBc.3961A>T (p.Lys1321Ter)
2g.151674503T>CCA348817670NEBc.3961A>G (p.Lys1321Glu)
2g.151674503T>GCA348817671NEBc.3961A>C (p.Lys1321Gln)
2g.151674504G>ACA429243043NEBc.3960C>T (p.Ala1320=)
2g.151674504G>CCA429243045NEBc.3960C>G (p.Ala1320=)
2g.151674504G>TCA429243046NEBc.3960C>A (p.Ala1320=)
2g.151674505G>ACA348817674NEBc.3959C>T (p.Ala1320Val)
gnomAD v4
2g.151674505G>CCA348817672NEBc.3959C>G (p.Ala1320Gly)
2g.151674505G>TCA348817673NEBc.3959C>A (p.Ala1320Asp)
2g.151674506C>ACA348817675NEBc.3958G>T (p.Ala1320Ser)
2g.151674506C>GCA348817676NEBc.3958G>C (p.Ala1320Pro)
2g.151674506C>TCA348817677NEBc.3958G>A (p.Ala1320Thr)
2g.151674507T>ACA429243048NEBc.3957A>T (p.Ala1319=)
2g.151674507T>CCA429243049NEBc.3957A>G (p.Ala1319=)
2g.151674507T>GCA429243050NEBc.3957A>C (p.Ala1319=)
2g.151674508G>ACA348817678NEBc.3956C>T (p.Ala1319Val)
2g.151674508G>CCA348817679NEBc.3956C>G (p.Ala1319Gly)
2g.151674508G>TCA348817680NEBc.3956C>A (p.Ala1319Glu)
2g.151674509C>ACA348817681NEBc.3955G>T (p.Ala1319Ser)
gnomAD v4
2g.151674509C>GCA348817682NEBc.3955G>C (p.Ala1319Pro)
2g.151674509C>TCA348817683NEBc.3955G>A (p.Ala1319Thr)
2g.151674510A>CCA429243052NEBc.3954T>G (p.Thr1318=)
2g.151674510A>GCA429243053NEBc.3954T>C (p.Thr1318=)
ClinVar dbSNP
2g.151674510A>TCA429243054NEBc.3954T>A (p.Thr1318=)
gnomAD v4
2g.151674511G>ACA348817684NEBc.3953C>T (p.Thr1318Ile)
2g.151674511G>CCA348817685NEBc.3953C>G (p.Thr1318Ser)
2g.151674511G>TCA348817686NEBc.3953C>A (p.Thr1318Asn)
2g.151674512T>ACA348817687NEBc.3952A>T (p.Thr1318Ser)
2g.151674512T>CCA348817689NEBc.3952A>G (p.Thr1318Ala)
2g.151674512T>GCA348817688NEBc.3952A>C (p.Thr1318Pro)
2g.151674513G>ACA429243059NEBc.3951C>T (p.Ile1317=)
2g.151674513G>CCA348817690NEBc.3951C>G (p.Ile1317Met)

Number of alleles fetched