Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.68157629C>TCA13649226IFNGc.366+284G>A (n.366+284G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.68157629C>ACA2043752627IFNGc.366+284G>T (n.366+284G>T)
dbSNP

Number of alleles fetched