Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25004210_25005726delCA2573158583ARXc.1449-816_*460del
ClinVar
Xg.25004734_25004841delCA2558513964ARXc.1521_1628del (p.Val508_Ala543del)
Xg.25004788G>ACA412610736ARXc.1571C>T (p.Ala524Val)
Xg.25004788G>CCA412610737ARXc.1571C>G (p.Ala524Gly)
Xg.25004788G>TCA412610738ARXc.1571C>A (p.Ala524Asp)
gnomAD v4
Xg.25004789C>ACA412610740ARXc.1570G>T (p.Ala524Ser)
gnomAD v4
Xg.25004789C>GCA412610741ARXc.1570G>C (p.Ala524Pro)
Xg.25004789C>TCA412610739ARXc.1570G>A (p.Ala524Thr)
Xg.25004790C>ACA515748067ARXc.1569G>T (p.Ala523=)
gnomAD v4
Xg.25004790C=CA2420205928ARXc.1569G= (p.Ala523=)
Xg.25004790C>GCA515748065ARXc.1569G>C (p.Ala523=)
ClinVar dbSNP
Xg.25004790C>TCA515748063ARXc.1569G>A (p.Ala523=)
ClinVar
Xg.25004791G>ACA412610742ARXc.1568C>T (p.Ala523Val)
ClinVar dbSNP gnomAD v4
Xg.25004791G>CCA412610743ARXc.1568C>G (p.Ala523Gly)
Xg.25004791G=CA2420205929ARXc.1568C= (p.Ala523=)
Xg.25004791G>TCA412610744ARXc.1568C>A (p.Ala523Glu)
gnomAD v4
Xg.25004792_25004796dupCA2695233367ARXc.1564_1568dup (p.Ala524ArgfsTer11)
Xg.25004792C>ACA412610745ARXc.1567G>T (p.Ala523Ser)
gnomAD v4
Xg.25004792C>GCA412610746ARXc.1567G>C (p.Ala523Pro)
gnomAD v4
Xg.25004792C>TCA412610747ARXc.1567G>A (p.Ala523Thr)
gnomAD v4
Xg.25004793C>ACA515748068ARXc.1566G>T (p.Thr522=)
gnomAD v4
Xg.25004793C=CA2420205930ARXc.1566G= (p.Thr522=)
Xg.25004793C>GCA515748070ARXc.1566G>C (p.Thr522=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25004793C>TCA515748069ARXc.1566G>A (p.Thr522=)
dbSNP gnomAD v3 gnomAD v4
Xg.25004794G>ACA412610748ARXc.1565C>T (p.Thr522Met)
gnomAD v4
Xg.25004794G>CCA412610750ARXc.1565C>G (p.Thr522Arg)
Xg.25004794G>TCA412610749ARXc.1565C>A (p.Thr522Lys)
gnomAD v4
Xg.25004795T>ACA412610751ARXc.1564A>T (p.Thr522Ser)
Xg.25004795T>CCA412610752ARXc.1564A>G (p.Thr522Ala)
dbSNP gnomAD v2 gnomAD v4
Xg.25004795T>GCA412610753ARXc.1564A>C (p.Thr522Pro)
Xg.25004795T=CA2420205931ARXc.1564A= (p.Thr522=)
Xg.25004796G>ACA10373767ARXc.1563C>T (p.Ala521=)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.25004796G>CCA515748071ARXc.1563C>G (p.Ala521=)
Xg.25004796G=CA2420205932ARXc.1563C= (p.Ala521=)
Xg.25004796G>TCA515748072ARXc.1563C>A (p.Ala521=)
gnomAD v4
Xg.25004797G>ACA412610754ARXc.1562C>T (p.Ala521Val)
gnomAD v4
Xg.25004797G>CCA412610756ARXc.1562C>G (p.Ala521Gly)
Xg.25004797G>TCA412610755ARXc.1562C>A (p.Ala521Asp)
Xg.25004798C>ACA412610757ARXc.1561G>T (p.Ala521Ser)
gnomAD v4
Xg.25004798C=CA2420205934ARXc.1561G= (p.Ala521=)
Xg.25004798C>GCA412610758ARXc.1561G>C (p.Ala521Pro)
gnomAD v4
Xg.25004798C>TCA206413ARXc.1561G>A (p.Ala521Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25004798_25004839delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGGCA2420205933ARXc.1520_1561delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG (p.Ala507=)
Xg.25004799C>ACA515748073ARXc.1560G>T (p.Pro520=)
gnomAD v4
Xg.25004799C=CA2420205935ARXc.1560G= (p.Pro520=)
Xg.25004799C>GCA515748074ARXc.1560G>C (p.Pro520=)
Xg.25004799C>TCA515748075ARXc.1560G>A (p.Pro520=)
dbSNP gnomAD v2
Xg.25004804_25004844delCA891843837ARXc.1520_1560del (p.Ala507GlyfsTer11)
ClinVar dbSNP
Xg.25004800G>ACA412610759ARXc.1559C>T (p.Pro520Leu)
dbSNP gnomAD v2 gnomAD v4
Xg.25004800G>CCA412610761ARXc.1559C>G (p.Pro520Arg)

Number of alleles fetched