Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.53810809G>ACA115098NLRP12c.850C>T (p.Arg284Ter)
c.682C>T (p.Arg228Ter)
c.433C>T (p.Arg145Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53810809G>CCA407415661NLRP12c.850C>G (p.Arg284Gly)
c.682C>G (p.Arg228Gly)
c.433C>G (p.Arg145Gly)
ClinVar dbSNP gnomAD v4
19g.53810809G=CA2342536901NLRP12c.850C= (p.Arg284=)
c.682C= (p.Arg228=)
c.433C= (p.Arg145=)
dbSNP

Number of alleles fetched