Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
2g.151674513G>TCA429243060NEBc.3951C>A (p.Ile1317=)
2g.151674514A=CA1298292943NEBc.3950T= (p.Ile1317=)
2g.151674514A>CCA348817691NEBc.3950T>G (p.Ile1317Ser)
2g.151674514A>GCA348817692NEBc.3950T>C (p.Ile1317Thr)
dbSNP gnomAD v3 gnomAD v4
2g.151674514A>TCA348817693NEBc.3950T>A (p.Ile1317Asn)
2g.151674515T>ACA348817694NEBc.3949A>T (p.Ile1317Phe)
2g.151674515T>CCA1910780NEBc.3949A>G (p.Ile1317Val)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.151674515T>GCA348817695NEBc.3949A>C (p.Ile1317Leu)
2g.151674515T=CA1298292946NEBc.3949A= (p.Ile1317=)
2g.151674516G>ACA429243064NEBc.3948C>T (p.Pro1316=)
2g.151674516G>CCA429243065NEBc.3948C>G (p.Pro1316=)
2g.151674516G>TCA429243066NEBc.3948C>A (p.Pro1316=)
2g.151674517G>ACA348817696NEBc.3947C>T (p.Pro1316Leu)
2g.151674517G>CCA348817697NEBc.3947C>G (p.Pro1316Arg)
2g.151674517G>TCA348817698NEBc.3947C>A (p.Pro1316His)
2g.151674518G>ACA348817699NEBc.3946C>T (p.Pro1316Ser)
dbSNP gnomAD v4
2g.151674518G>CCA348817700NEBc.3946C>G (p.Pro1316Ala)
gnomAD v4
2g.151674518G=CA1298292948NEBc.3946C= (p.Pro1316=)
2g.151674518G>TCA348817701NEBc.3946C>A (p.Pro1316Thr)
2g.151674518_151674519insCCCA2661470371NEBc.3945_3946insGG (p.Pro1316GlyfsTer?)
gnomAD v4
2g.151674519A>CCA348817702NEBc.3945T>G (p.Ile1315Met)
2g.151674519A>GCA429243070NEBc.3945T>C (p.Ile1315=)
2g.151674519A>TCA429243071NEBc.3945T>A (p.Ile1315=)
2g.151674519_151674521delinsCCACA2580064127NEBc.3943_3945delinsTGG (p.Ile1315Trp)
ClinVar
2g.151674520A>CCA348817703NEBc.3944T>G (p.Ile1315Ser)
2g.151674520A>GCA348817704NEBc.3944T>C (p.Ile1315Thr)
2g.151674520A>TCA348817705NEBc.3944T>A (p.Ile1315Asn)
2g.151674521_151674522delCA2661470372NEBc.3943_3944del (p.Ile1315SerfsTer14)
gnomAD v4
2g.151674521T>ACA348817706NEBc.3943A>T (p.Ile1315Phe)
2g.151674521T>CCA348817707NEBc.3943A>G (p.Ile1315Val)
ClinVar gnomAD v4
2g.151674521T>GCA348817708NEBc.3943A>C (p.Ile1315Leu)
gnomAD v4
2g.151674522A=CA1298292950NEBc.3942T= (p.Ala1314=)
2g.151674522A>CCA429243076NEBc.3942T>G (p.Ala1314=)
2g.151674522A>GCA429243074NEBc.3942T>C (p.Ala1314=)
2g.151674522A>TCA429243075NEBc.3942T>A (p.Ala1314=)
dbSNP
2g.151674523G>ACA348817709NEBc.3941C>T (p.Ala1314Val)

Number of alleles fetched