Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.70853148C>ACA516759766TEX11c.411G>T (p.Leu137=)
c.456G>T (p.Leu152=)
Xg.70853148C>GCA516759767TEX11c.411G>C (p.Leu137=)
c.456G>C (p.Leu152=)
Xg.70853148C>TCA516759768TEX11c.411G>A (p.Leu137=)
c.456G>A (p.Leu152=)
Xg.70853149A>CCA413607992TEX11c.410T>G (p.Leu137Arg)
c.455T>G (p.Leu152Arg)
Xg.70853149A>GCA413607993TEX11c.410T>C (p.Leu137Pro)
c.455T>C (p.Leu152Pro)
Xg.70853149A>TCA413607994TEX11c.410T>A (p.Leu137Gln)
c.455T>A (p.Leu152Gln)
Xg.70853150G>ACA10442904TEX11c.409C>T (p.Leu137=)
c.454C>T (p.Leu152=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853150G>CCA413607995TEX11c.409C>G (p.Leu137Val)
c.454C>G (p.Leu152Val)
gnomAD v4
Xg.70853150G=CA2436261239TEX11c.409C= (p.Leu137=)
c.454C= (p.Leu152=)
Xg.70853150G>TCA413607996TEX11c.409C>A (p.Leu137Met)
c.454C>A (p.Leu152Met)
Xg.70853151A>CCA413607997TEX11c.408T>G (p.Ser136Arg)
c.453T>G (p.Ser151Arg)
Xg.70853151A>GCA516759793TEX11c.408T>C (p.Ser136=)
c.453T>C (p.Ser151=)
Xg.70853151A>TCA413607998TEX11c.408T>A (p.Ser136Arg)
c.453T>A (p.Ser151Arg)
Xg.70853152C>ACA413608001TEX11c.407G>T (p.Ser136Ile)
c.452G>T (p.Ser151Ile)
Xg.70853152C>GCA413608000TEX11c.407G>C (p.Ser136Thr)
c.452G>C (p.Ser151Thr)
Xg.70853152C>TCA413607999TEX11c.407G>A (p.Ser136Asn)
c.452G>A (p.Ser151Asn)
Xg.70853153T>ACA413608002TEX11c.406A>T (p.Ser136Cys)
c.451A>T (p.Ser151Cys)
Xg.70853153T>CCA413608003TEX11c.406A>G (p.Ser136Gly)
c.451A>G (p.Ser151Gly)
Xg.70853153T>GCA413608004TEX11c.406A>C (p.Ser136Arg)
c.451A>C (p.Ser151Arg)
Xg.70853154C>ACA413608005TEX11c.406-1G>T (n.406-1G>T)
c.451-1G>T (n.451-1G>T)
Xg.70853154C>GCA413608006TEX11c.406-1G>C (n.406-1G>C)
c.451-1G>C (n.451-1G>C)
Xg.70853154C>TCA413608007TEX11c.406-1G>A (n.406-1G>A)
c.451-1G>A (n.451-1G>A)
Xg.70853155T>ACA413608008TEX11c.406-2A>T (n.406-2A>T)
c.451-2A>T (n.451-2A>T)
Xg.70853155T>CCA413608009TEX11c.406-2A>G (n.406-2A>G)
c.451-2A>G (n.451-2A>G)
Xg.70853155T>GCA413608010TEX11c.406-2A>C (n.406-2A>C)
c.451-2A>C (n.451-2A>C)
Xg.70853160A=CA2436261240TEX11c.406-7T= (n.406-7T=)
c.451-7T= (n.451-7T=)
Xg.70853160A>GCA877775999TEX11c.406-7T>C (n.406-7T>C)
c.451-7T>C (n.451-7T>C)
dbSNP gnomAD v4
Xg.70853161A=CA2436261241TEX11c.406-8T= (n.406-8T=)
c.451-8T= (n.451-8T=)
Xg.70853161A>TCA2436261242TEX11c.406-8T>A (n.406-8T>A)
c.451-8T>A (n.451-8T>A)
dbSNP
Xg.70853162T>CCA10442905TEX11c.406-9A>G (n.406-9A>G)
c.451-9A>G (n.451-9A>G)
dbSNP ExAC
Xg.70853162T=CA2436261243TEX11c.406-9A= (n.406-9A=)
c.451-9A= (n.451-9A=)
Xg.70853165A=CA2436261244TEX11c.406-12T= (n.406-12T=)
c.451-12T= (n.451-12T=)
Xg.70853165A>GCA642470359TEX11c.406-12T>C (n.406-12T>C)
c.451-12T>C (n.451-12T>C)
dbSNP gnomAD v2 gnomAD v4
Xg.70853168dupCA2694012961TEX11c.406-13dup (n.406-13dup)
c.451-13dup (n.451-13dup)
gnomAD v4
Xg.70853169A=CA2436261245TEX11c.406-16T= (n.406-16T=)
c.451-16T= (n.451-16T=)
Xg.70853169A>CCA2436261246TEX11c.406-16T>G (n.406-16T>G)
c.451-16T>G (n.451-16T>G)
dbSNP gnomAD v4
Xg.70853172G>ACA2579637143TEX11c.406-19C>T (n.406-19C>T)
c.451-19C>T (n.451-19C>T)
gnomAD v4
Xg.70853174A>GCA2694012962TEX11c.406-21T>C (n.406-21T>C)
c.451-21T>C (n.451-21T>C)
gnomAD v4
Xg.70853177_70853178delinsATCA2436261247TEX11c.406-25_406-24delinsAT (n.406-25_406-24delinsAT)
c.451-25_451-24delinsAT (n.451-25_451-24delinsAT)
Xg.70853178delCA642470360TEX11c.406-25del (n.406-25del)
c.451-25del (n.451-25del)
dbSNP gnomAD v2 gnomAD v4
Xg.70853183C>ACA642470361TEX11c.406-30G>T (n.406-30G>T)
c.451-30G>T (n.451-30G>T)
dbSNP gnomAD v2 gnomAD v4
Xg.70853183C=CA2436261248TEX11c.406-30G= (n.406-30G=)
c.451-30G= (n.451-30G=)
Xg.70853184A=CA2436261249TEX11c.406-31T= (n.406-31T=)
c.451-31T= (n.451-31T=)
Xg.70853184A>CCA331002040TEX11c.406-31T>G (n.406-31T>G)
c.451-31T>G (n.451-31T>G)
dbSNP gnomAD v2 gnomAD v4
Xg.70853184A>TCA2436261250TEX11c.406-31T>A (n.406-31T>A)
c.451-31T>A (n.451-31T>A)
dbSNP
Xg.70853185A>GCA2694012963TEX11c.406-32T>C (n.406-32T>C)
c.451-32T>C (n.451-32T>C)
gnomAD v4
Xg.70853186T>CCA2579637144TEX11c.406-33A>G (n.406-33A>G)
c.451-33A>G (n.451-33A>G)
Xg.70853189G>ACA642470362TEX11c.406-36C>T (n.406-36C>T)
c.451-36C>T (n.451-36C>T)
dbSNP gnomAD v2 gnomAD v4
Xg.70853189G=CA2436261251TEX11c.406-36C= (n.406-36C=)
c.451-36C= (n.451-36C=)
Xg.70853189_70853192delinsGAATCA2436261252TEX11c.406-39_406-36delinsATTC (n.406-39_406-36delinsATTC)
c.451-39_451-36delinsATTC (n.451-39_451-36delinsATTC)

Number of alleles fetched