Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.142877011C>TCA4905393CYP11B1,GMLc.595+12G>A (p.=)
c.673+12G>A (p.=)
c.412+12G>A (p.=)
c.214+35786C>T (p.=)
n.628+12G>A
c.808+12G>A (p.=)
c.181+35786C>T (p.=)
ClinVar dbSNP ExAC gnomAD
8g.142877011C>GCA4905394CYP11B1,GMLc.595+12G>C (p.=)
c.673+12G>C (p.=)
c.412+12G>C (p.=)
c.214+35786C>G (p.=)
n.628+12G>C
c.808+12G>C (p.=)
c.181+35786C>G (p.=)
dbSNP ExAC gnomAD

Number of alleles fetched