Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434752G>ACA065105WT1c.609C>T (p.Asn203=)
c.594C>T (p.Asn198=)
n.788C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434752G>CCA16613601WT1c.609C>G (p.Asn203Lys)
c.594C>G (p.Asn198Lys)
n.788C>G
ClinVar dbSNP gnomAD v4
11g.32434752G>TCA379964538WT1c.609C>A (p.Asn203Lys)
c.594C>A (p.Asn198Lys)
n.788C>A
ClinVar dbSNP gnomAD v4
11g.32434752G=CA1962327112WT1c.609C= (p.Asn203=)
c.594C= (p.Asn198=)
n.788C=
dbSNP

Number of alleles fetched