Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012021_25015415delCA915950806ARXc.196+129_1073+903del
ClinVar
Xg.25013332_25013337dupCA10577657ARXc.665_670dup (p.Thr223_Glu224insGlyThr)
dbSNP gnomAD v3 gnomAD v4
Xg.25013332G>ACA16608870ARXc.663C>T (p.Thr221=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013332G>CCA515947837ARXc.663C>G (p.Thr221=)
ClinVar dbSNP gnomAD v4
Xg.25013332G=CA2420209216ARXc.663C= (p.Thr221=)
Xg.25013332G>TCA515947841ARXc.663C>A (p.Thr221=)
Xg.25013333G>ACA327733050ARXc.662C>T (p.Thr221Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013333G>CCA412612710ARXc.662C>G (p.Thr221Ser)
Xg.25013333G=CA2420209217ARXc.662C= (p.Thr221=)
Xg.25013333G>TCA412612709ARXc.662C>A (p.Thr221Asn)
gnomAD v4
Xg.25013334T>ACA412612711ARXc.661A>T (p.Thr221Ser)
Xg.25013334T>CCA224135ARXc.661A>G (p.Thr221Ala)
dbSNP
Xg.25013334T>GCA412612712ARXc.661A>C (p.Thr221Pro)
Xg.25013334T=CA2420209218ARXc.661A= (p.Thr221=)
Xg.25013335G>ACA515947854ARXc.660C>T (p.Gly220=)
gnomAD v4
Xg.25013335G>CCA515947855ARXc.660C>G (p.Gly220=)
Xg.25013335G>TCA515947853ARXc.660C>A (p.Gly220=)
gnomAD v4
Xg.25013336C>ACA412612713ARXc.659G>T (p.Gly220Val)
Xg.25013336C>GCA412612714ARXc.659G>C (p.Gly220Ala)
ClinVar dbSNP gnomAD v4
Xg.25013336C>TCA412612715ARXc.659G>A (p.Gly220Asp)
ClinVar gnomAD v4
Xg.25013337C>ACA412612716ARXc.658G>T (p.Gly220Cys)
gnomAD v4
Xg.25013337C=CA2420209219ARXc.658G= (p.Gly220=)
Xg.25013337C>GCA412612717ARXc.658G>C (p.Gly220Arg)
Xg.25013337C>TCA412612718ARXc.658G>A (p.Gly220Ser)
dbSNP gnomAD v3 gnomAD v4
Xg.25013338A=CA2420209220ARXc.657T= (p.Gly219=)
Xg.25013338A>CCA515947866ARXc.657T>G (p.Gly219=)
Xg.25013338A>GCA10373889ARXc.657T>C (p.Gly219=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013338A>TCA515947865ARXc.657T>A (p.Gly219=)
gnomAD v4
Xg.25013339C>ACA412612719ARXc.656G>T (p.Gly219Val)
gnomAD v4
Xg.25013339C>GCA412612720ARXc.656G>C (p.Gly219Ala)
Xg.25013339C>TCA412612721ARXc.656G>A (p.Gly219Asp)
Xg.25013340C>ACA412612722ARXc.655G>T (p.Gly219Cys)
Xg.25013340C>GCA412612724ARXc.655G>C (p.Gly219Arg)
Xg.25013340C>TCA412612723ARXc.655G>A (p.Gly219Ser)
gnomAD v4
Xg.25013341A>CCA515947876ARXc.654T>G (p.Gly218=)
Xg.25013341A>GCA515947880ARXc.654T>C (p.Gly218=)
Xg.25013341A>TCA515947879ARXc.654T>A (p.Gly218=)
Xg.25013342C>ACA412612725ARXc.653G>T (p.Gly218Val)
ClinVar
Xg.25013342C=CA2420209221ARXc.653G= (p.Gly218=)
Xg.25013342C>GCA412612726ARXc.653G>C (p.Gly218Ala)
Xg.25013342C>TCA412612727ARXc.653G>A (p.Gly218Asp)
dbSNP gnomAD v4
Xg.25013343C>ACA412612728ARXc.652G>T (p.Gly218Cys)
Xg.25013343C>GCA412612729ARXc.652G>C (p.Gly218Arg)
Xg.25013343C>TCA412612730ARXc.652G>A (p.Gly218Ser)
Xg.25013344C>ACA171160ARXc.651G>T (p.Ala217=)
ClinVar dbSNP gnomAD v4 COSMIC
Xg.25013344C=CA2420209222ARXc.651G= (p.Ala217=)
Xg.25013344C>GCA515947885ARXc.651G>C (p.Ala217=)
Xg.25013344C>TCA515947887ARXc.651G>A (p.Ala217=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013345G>ACA412612731ARXc.650C>T (p.Ala217Val)
dbSNP gnomAD v4
Xg.25013345G>CCA412612732ARXc.650C>G (p.Ala217Gly)

Number of alleles fetched