Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.64813377C>ACA275110EYSc.3443+1G>T (n.3443+1G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.64813377C>TCA364786663EYSc.3443+1G>A (n.3443+1G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.64813377C=CA1633921274EYSc.3443+1G= (n.3443+1G=)
dbSNP

Number of alleles fetched