Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47447853G>ACA119256RAPSNc.490C>T (p.Arg164Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.47447853G>CCA380333737RAPSNc.490C>G (p.Arg164Gly)
 ClinVar dbSNP
11g.47447853G=CA1969390440RAPSNc.490C= (p.Arg164=)
 dbSNP

Number of alleles fetched