Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.109595182G>ACA210347MVKc.1039+1G>A (p.=)
c.883+1G>A (p.=)
c.*486+1G>A (p.=)
c.*712+1G>A (p.=)
c.196+1G>A (p.=)
n.3272+1G>A
ClinVar dbSNP
12g.109595182G>TCA149770MVKc.1039+1G>T (p.=)
c.883+1G>T (p.=)
c.*486+1G>T (p.=)
c.*712+1G>T (p.=)
c.196+1G>T (p.=)
n.3272+1G>T
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched