Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012021_25015415delCA915950806ARXc.196+129_1073+903del
ClinVar
Xg.25013352_25013381delinsGGGCGCTGCCCGGGCCGCCGGCCACGCCGACA2420209227ARXc.614_643delinsTCGGCGTGGCCGGCGGCCCGGGCAGCGCCC (p.Leu205=)
Xg.25013359_25013387delCA10605871ARXc.614_642del (p.Leu205ProfsTer23)
ClinVar dbSNP
Xg.25013381A>CCA412612801ARXc.614T>G (p.Leu205Arg)
Xg.25013381A>GCA412612802ARXc.614T>C (p.Leu205Pro)
Xg.25013381A>TCA412612803ARXc.614T>A (p.Leu205His)
Xg.25013382G>ACA207632ARXc.613C>T (p.Leu205Phe)
ClinVar dbSNP gnomAD v4
Xg.25013382G>CCA412612804ARXc.613C>G (p.Leu205Val)
Xg.25013382G=CA2420209242ARXc.613C= (p.Leu205=)
Xg.25013382G>TCA412612805ARXc.613C>A (p.Leu205Ile)
Xg.25013383G>ACA515948069ARXc.612C>T (p.Arg204=)
Xg.25013383G>CCA515948070ARXc.612C>G (p.Arg204=)
Xg.25013383G>TCA515948071ARXc.612C>A (p.Arg204=)
gnomAD v4
Xg.25013384C>ACA412612806ARXc.611G>T (p.Arg204Leu)
ClinVar dbSNP gnomAD v4
Xg.25013384C=CA2420209243ARXc.611G= (p.Arg204=)
Xg.25013384C>GCA412612807ARXc.611G>C (p.Arg204Pro)
ClinVar gnomAD v4
Xg.25013384C>TCA10373892ARXc.611G>A (p.Arg204His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013385G>ACA412612808ARXc.610C>T (p.Arg204Cys)
ClinVar gnomAD v4
Xg.25013385G>CCA412612809ARXc.610C>G (p.Arg204Gly)
gnomAD v4
Xg.25013385G=CA2420209244ARXc.610C= (p.Arg204=)
Xg.25013385G>TCA10373893ARXc.610C>A (p.Arg204Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013386C>ACA412612810ARXc.609G>T (p.Glu203Asp)
gnomAD v4
Xg.25013386C>GCA412612811ARXc.609G>C (p.Glu203Asp)
Xg.25013386C>TCA515948086ARXc.609G>A (p.Glu203=)
Xg.25013387T>ACA412612812ARXc.608A>T (p.Glu203Val)
Xg.25013387T>CCA412612813ARXc.608A>G (p.Glu203Gly)
gnomAD v4
Xg.25013387T>GCA412612814ARXc.608A>C (p.Glu203Ala)
Xg.25013388C>ACA412612815ARXc.607G>T (p.Glu203Ter)
gnomAD v4
Xg.25013388C>GCA412612816ARXc.607G>C (p.Glu203Gln)
Xg.25013388C>TCA412612817ARXc.607G>A (p.Glu203Lys)
gnomAD v4
Xg.25013389C>ACA412612819ARXc.606G>T (p.Glu202Asp)
gnomAD v4
Xg.25013389C>GCA412612818ARXc.606G>C (p.Glu202Asp)
ClinVar
Xg.25013389C>TCA515948103ARXc.606G>A (p.Glu202=)
Xg.25013390T>ACA412612820ARXc.605A>T (p.Glu202Val)
Xg.25013390T>CCA412612821ARXc.605A>G (p.Glu202Gly)
Xg.25013390T>GCA412612822ARXc.605A>C (p.Glu202Ala)
Xg.25013391C>ACA412612823ARXc.604G>T (p.Glu202Ter)
Xg.25013391C>GCA412612824ARXc.604G>C (p.Glu202Gln)
Xg.25013391C>TCA412612825ARXc.604G>A (p.Glu202Lys)
Xg.25013392C>ACA515948113ARXc.603G>T (p.Pro201=)
gnomAD v4
Xg.25013392C=CA2420209245ARXc.603G= (p.Pro201=)
Xg.25013392C>GCA515948114ARXc.603G>C (p.Pro201=)
Xg.25013392C>TCA515948117ARXc.603G>A (p.Pro201=)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25013393G>ACA412612828ARXc.602C>T (p.Pro201Leu)
dbSNP
Xg.25013393G>CCA412612827ARXc.602C>G (p.Pro201Arg)
Xg.25013393G=CA2420209246ARXc.602C= (p.Pro201=)
Xg.25013393G>TCA412612826ARXc.602C>A (p.Pro201Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25013394G>ACA412612829ARXc.601C>T (p.Pro201Ser)
Xg.25013394G>CCA412612830ARXc.601C>G (p.Pro201Ala)
Xg.25013394G=CA2420209247ARXc.601C= (p.Pro201=)

Number of alleles fetched