Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7172363G>ACA124250INSRc.1195C>T (p.Arg399Ter)
n.1170C>T
c.1273C>T (p.Arg425Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.7172363G=CA2320790729INSRc.1195C= (p.Arg399=)
n.1170C=
c.1273C= (p.Arg425=)
 dbSNP

Number of alleles fetched