Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50627247_50627257delCA2657593856ARSAc.374_384del (p.Lys125ArgfsTer5)
c.116_126del (p.Lys39ArgfsTer5)
n.765_775del
gnomAD v4
22g.50627250G>ACA515391480ARSAc.381C>T (p.His127=)
c.123C>T (p.His41=)
n.772C>T
dbSNP gnomAD v2 gnomAD v4
22g.50627250G>CCA412180700ARSAc.381C>G (p.His127Gln)
c.123C>G (p.His41Gln)
n.772C>G
22g.50627250G=CA2410959509ARSAc.381C= (p.His127=)
c.123C= (p.His41=)
n.772C=
22g.50627250G>TCA412180701ARSAc.381C>A (p.His127Gln)
c.123C>A (p.His41Gln)
n.772C>A
22g.50627251T>ACA412180704ARSAc.380A>T (p.His127Leu)
c.122A>T (p.His41Leu)
n.771A>T
22g.50627251T>CCA412180706ARSAc.380A>G (p.His127Arg)
c.122A>G (p.His41Arg)
n.771A>G
22g.50627251T>GCA412180707ARSAc.380A>C (p.His127Pro)
c.122A>C (p.His41Pro)
n.771A>C
22g.50627252G>ACA412180708ARSAc.379C>T (p.His127Tyr)
c.121C>T (p.His41Tyr)
n.770C>T
22g.50627252G>CCA412180709ARSAc.379C>G (p.His127Asp)
c.121C>G (p.His41Asp)
n.770C>G
22g.50627252G>TCA412180712ARSAc.379C>A (p.His127Asn)
c.121C>A (p.His41Asn)
n.770C>A
22g.50627253C>ACA412180715ARSAc.378G>T (p.Trp126Cys)
c.120G>T (p.Trp40Cys)
n.769G>T
22g.50627253C=CA2410959510ARSAc.378G= (p.Trp126=)
c.120G= (p.Trp40=)
n.769G=
22g.50627253C>GCA412180718ARSAc.378G>C (p.Trp126Cys)
c.120G>C (p.Trp40Cys)
n.769G>C
22g.50627253C>TCA412180720ARSAc.378G>A (p.Trp126Ter)
c.120G>A (p.Trp40Ter)
n.769G>A
ClinVar dbSNP gnomAD v4
22g.50627254C>ACA412180729ARSAc.377G>T (p.Trp126Leu)
c.119G>T (p.Trp40Leu)
n.768G>T
22g.50627254C>GCA412180733ARSAc.377G>C (p.Trp126Ser)
c.119G>C (p.Trp40Ser)
n.768G>C
22g.50627254C>TCA412180722ARSAc.377G>A (p.Trp126Ter)
c.119G>A (p.Trp40Ter)
n.768G>A
22g.50627255A=CA2410959511ARSAc.376T= (p.Trp126=)
c.118T= (p.Trp40=)
n.767T=
22g.50627255A>CCA412180738ARSAc.376T>G (p.Trp126Gly)
c.118T>G (p.Trp40Gly)
n.767T>G
dbSNP
22g.50627255A>GCA412180736ARSAc.376T>C (p.Trp126Arg)
c.118T>C (p.Trp40Arg)
n.767T>C
22g.50627255A>TCA412180737ARSAc.376T>A (p.Trp126Arg)
c.118T>A (p.Trp40Arg)
n.767T>A
gnomAD v4
22g.50627256C>ACA412180740ARSAc.375G>T (p.Lys125Asn)
c.117G>T (p.Lys39Asn)
n.766G>T
22g.50627256C=CA2410959513ARSAc.375G= (p.Lys125=)
c.117G= (p.Lys39=)
n.766G=
22g.50627256C>GCA412180743ARSAc.375G>C (p.Lys125Asn)
c.117G>C (p.Lys39Asn)
n.766G>C
dbSNP gnomAD v3 gnomAD v4
22g.50627256C>TCA515391485ARSAc.375G>A (p.Lys125=)
c.117G>A (p.Lys39=)
n.766G>A
22g.50627256_50627262delinsCTTGCCGCA2410959512ARSAc.369_375delinsCGGCAAG (p.Ala123=)
c.111_117delinsCGGCAAG (p.Ala37=)
n.760_766delinsCGGCAAG
22g.50627257T>ACA412180753ARSAc.374A>T (p.Lys125Met)
c.116A>T (p.Lys39Met)
n.765A>T
22g.50627257T>CCA412180756ARSAc.374A>G (p.Lys125Arg)
c.116A>G (p.Lys39Arg)
n.765A>G
22g.50627257T>GCA412180758ARSAc.374A>C (p.Lys125Thr)
c.116A>C (p.Lys39Thr)
n.765A>C
ClinVar
22g.50627257_50627262delinsCCCAAGGTTCA233479ARSAc.369_374delinsAACCTTGGG (p.Gly124_Lys125delinsThrLeuGly)
c.111_116delinsAACCTTGGG (p.Gly38_Lys39delinsThrLeuGly)
n.760_765delinsAACCTTGGG
ClinVar dbSNP
22g.50627258T>ACA412180763ARSAc.373A>T (p.Lys125Ter)
c.115A>T (p.Lys39Ter)
n.764A>T
22g.50627258T>CCA412180767ARSAc.373A>G (p.Lys125Glu)
c.115A>G (p.Lys39Glu)
n.764A>G
22g.50627258T>GCA412180770ARSAc.373A>C (p.Lys125Gln)
c.115A>C (p.Lys39Gln)
n.764A>C
22g.50627259G>ACA515391487ARSAc.372C>T (p.Gly124=)
c.114C>T (p.Gly38=)
n.763C>T
22g.50627259G>CCA515391488ARSAc.372C>G (p.Gly124=)
c.114C>G (p.Gly38=)
n.763C>G
22g.50627259G>TCA515391489ARSAc.372C>A (p.Gly124=)
c.114C>A (p.Gly38=)
n.763C>A
gnomAD v4
22g.50627260C>ACA412180780ARSAc.371G>T (p.Gly124Val)
c.113G>T (p.Gly38Val)
n.762G>T
22g.50627260C=CA2410959514ARSAc.371G= (p.Gly124=)
c.113G= (p.Gly38=)
n.762G=
22g.50627260C>GCA412180775ARSAc.371G>C (p.Gly124Ala)
c.113G>C (p.Gly38Ala)
n.762G>C
22g.50627260C>TCA412180773ARSAc.371G>A (p.Gly124Asp)
c.113G>A (p.Gly38Asp)
n.762G>A
ClinVar dbSNP gnomAD v4
22g.50627261C>ACA325531581ARSAc.370G>T (p.Gly124Cys)
c.112G>T (p.Gly38Cys)
n.761G>T
ClinVar dbSNP gnomAD v4
22g.50627261C=CA2410959515ARSAc.370G= (p.Gly124=)
c.112G= (p.Gly38=)
n.761G=
22g.50627261C>GCA412180784ARSAc.370G>C (p.Gly124Arg)
c.112G>C (p.Gly38Arg)
n.761G>C
dbSNP gnomAD v4
22g.50627261C>TCA220987ARSAc.370G>A (p.Gly124Ser)
c.112G>A (p.Gly38Ser)
n.761G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50627261_50627262delinsCGCA2410959516ARSAc.369_370delinsCG (p.Ala123=)
c.111_112delinsCG (p.Ala37=)
n.760_761delinsCG
22g.50627262G>ACA10653701ARSAc.369C>T (p.Ala123=)
c.111C>T (p.Ala37=)
n.760C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50627262G>CCA515391492ARSAc.369C>G (p.Ala123=)
c.111C>G (p.Ala37=)
n.760C>G
22g.50627262G=CA2410959517ARSAc.369C= (p.Ala123=)
c.111C= (p.Ala37=)
n.760C=
22g.50627262G>TCA515391494ARSAc.369C>A (p.Ala123=)
c.111C>A (p.Ala37=)
n.760C>A

Number of alleles fetched