Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012021_25015415delCA915950806ARXc.196+129_1073+903del
ClinVar
Xg.25013447A>CCA412612933ARXc.548T>G (p.Val183Gly)
Xg.25013447A>GCA412612934ARXc.548T>C (p.Val183Ala)
gnomAD v4
Xg.25013447A>TCA412612935ARXc.548T>A (p.Val183Glu)
Xg.25013448C>ACA412612936ARXc.547G>T (p.Val183Leu)
gnomAD v4
Xg.25013448C>GCA412612937ARXc.547G>C (p.Val183Leu)
ClinVar
Xg.25013448C>TCA412612938ARXc.547G>A (p.Val183Met)
gnomAD v4
Xg.25013449G>ACA515948284ARXc.546C>T (p.Phe182=)
gnomAD v4
Xg.25013449G>CCA412612940ARXc.546C>G (p.Phe182Leu)
Xg.25013449G>TCA412612939ARXc.546C>A (p.Phe182Leu)
gnomAD v4
Xg.25013450A>CCA412612941ARXc.545T>G (p.Phe182Cys)
Xg.25013450A>GCA412612942ARXc.545T>C (p.Phe182Ser)
gnomAD v4
Xg.25013450A>TCA412612943ARXc.545T>A (p.Phe182Tyr)
gnomAD v4
Xg.25013451delCA2693353702ARXc.545del (p.Phe182SerfsTer?)
gnomAD v4
Xg.25013451A>CCA412612944ARXc.544T>G (p.Phe182Val)
gnomAD v4
Xg.25013451A>GCA412612945ARXc.544T>C (p.Phe182Leu)
gnomAD v4
Xg.25013451A>TCA412612946ARXc.544T>A (p.Phe182Ile)
gnomAD v4
Xg.25013452G>ACA289511ARXc.543C>T (p.Pro181=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25013452G>CCA515948293ARXc.543C>G (p.Pro181=)
Xg.25013452G=CA2420209275ARXc.543C= (p.Pro181=)
Xg.25013452G>TCA515948294ARXc.543C>A (p.Pro181=)
gnomAD v4
Xg.25013453G>ACA412612947ARXc.542C>T (p.Pro181Leu)
gnomAD v4
Xg.25013453G>CCA412612948ARXc.542C>G (p.Pro181Arg)
Xg.25013453G>TCA412612949ARXc.542C>A (p.Pro181His)
gnomAD v4
Xg.25013454G>ACA412612950ARXc.541C>T (p.Pro181Ser)
ClinVar gnomAD v4
Xg.25013454G>CCA412612951ARXc.541C>G (p.Pro181Ala)
gnomAD v4
Xg.25013454G>TCA412612952ARXc.541C>A (p.Pro181Thr)
ClinVar dbSNP gnomAD v4
Xg.25013455C>ACA241831ARXc.540G>T (p.Ala180=)
ClinVar dbSNP gnomAD v4
Xg.25013455C=CA2420209276ARXc.540G= (p.Ala180=)
Xg.25013455C>GCA515947493ARXc.540G>C (p.Ala180=)
dbSNP gnomAD v3 gnomAD v4
Xg.25013455C>TCA515947492ARXc.540G>A (p.Ala180=)
ClinVar dbSNP gnomAD v4
Xg.25013456G>ACA412612954ARXc.539C>T (p.Ala180Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013456G>CCA412612953ARXc.539C>G (p.Ala180Gly)
gnomAD v4
Xg.25013456G=CA2420209277ARXc.539C= (p.Ala180=)
Xg.25013456G>TCA412612955ARXc.539C>A (p.Ala180Glu)
gnomAD v4
Xg.25013457C>ACA412612956ARXc.538G>T (p.Ala180Ser)
gnomAD v4
Xg.25013457C=CA2420209278ARXc.538G= (p.Ala180=)
Xg.25013457C>GCA412612957ARXc.538G>C (p.Ala180Pro)
dbSNP
Xg.25013457C>TCA412612958ARXc.538G>A (p.Ala180Thr)
gnomAD v4
Xg.25013460delCA2693353703ARXc.538del (p.Ala180ArgfsTer?)
gnomAD v4
Xg.25013458C>ACA515947498ARXc.537G>T (p.Gly179=)
gnomAD v4
Xg.25013458C>GCA515947499ARXc.537G>C (p.Gly179=)
gnomAD v4
Xg.25013458C>TCA515947500ARXc.537G>A (p.Gly179=)
gnomAD v4
Xg.25013459C>ACA412612959ARXc.536G>T (p.Gly179Val)
dbSNP gnomAD v2 gnomAD v4
Xg.25013459C=CA2420209279ARXc.536G= (p.Gly179=)
Xg.25013459C>GCA412612960ARXc.536G>C (p.Gly179Ala)
gnomAD v4
Xg.25013459C>TCA412612961ARXc.536G>A (p.Gly179Glu)
gnomAD v4
Xg.25013460C>ACA412612962ARXc.535G>T (p.Gly179Trp)
gnomAD v4
Xg.25013460C=CA2420209280ARXc.535G= (p.Gly179=)
Xg.25013460C>GCA412612963ARXc.535G>C (p.Gly179Arg)
ClinVar dbSNP

Number of alleles fetched