Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2160825G>ACA5818186INS,INS-IGF2c.147C>T (p.Phe49=)
n.206C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2160825G>CCA123073INS,INS-IGF2c.147C>G (p.Phe49Leu)
n.206C>G
ClinVar dbSNP gnomAD v4

Number of alleles fetched