Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.24285390G>ACA4190742NPYc.150G>A (p.Ser50=)
c.42-29691C>T (n.42-29691C>T)
n.473+33967C>T
n.345-88361C>T
n.345-29691C>T
ClinVar dbSNP ExAC gnomAD
7g.24285390G>CCA155829098NPYc.150G>C (p.Ser50=)
c.42-29691C>G (n.42-29691C>G)
n.473+33967C>G
n.345-88361C>G
n.345-29691C>G
dbSNP
7g.24285390G>TCA4190743NPYc.150G>T (p.Ser50=)
c.42-29691C>A (n.42-29691C>A)
n.473+33967C>A
n.345-88361C>A
n.345-29691C>A
dbSNP ExAC gnomAD

Number of alleles fetched