Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.179559711G>ACA199102NPHS2c.502C>T (p.Arg168Cys)
c.325C>T (p.Arg109Cys)
c.429C>T (p.Phe143=)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
1g.179559711G=CA1210320283NPHS2c.502C= (p.Arg168=)
c.325C= (p.Arg109=)
c.429C= (p.Phe143=)
 dbSNP

Number of alleles fetched