Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.176094614C>GCA10576048HOXD13c.916C>G (p.Arg306Gly)
c.859C>G (p.Arg287Gly)
 ClinVar dbSNP
2g.176094614C>TCA124417HOXD13c.916C>T (p.Arg306Trp)
c.859C>T (p.Arg287Trp)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC

Number of alleles fetched