Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.44375168C>TCA1543137049FGF10c.325+13190G>A (n.325+13190G>A)
dbSNP
5g.44375168C>GCA118168754FGF10c.325+13190G>C (n.325+13190G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.44375168C>ACA1543137050FGF10c.325+13190G>T (n.325+13190G>T)
dbSNP

Number of alleles fetched