Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.43047635C>TCA003615BRCA1c.5467+8G>A (p.=)
c.5326+8G>A (p.=)
c.2155+8G>A (p.=)
c.2081+8G>A (p.=)
c.5530+8G>A (p.=)
n.5603+8G>A
c.2041+8G>A (p.=)
c.*5250+8G>A (p.=)
c.397+8G>A (p.=)
c.940+8G>A (p.=)
c.166+8G>A (p.=)
ClinVar dbSNP ExAC gnomAD
17g.43047635C>ACA003616BRCA1c.5467+8G>T (p.=)
c.5326+8G>T (p.=)
c.2155+8G>T (p.=)
c.2081+8G>T (p.=)
c.5530+8G>T (p.=)
n.5603+8G>T
c.2041+8G>T (p.=)
c.*5250+8G>T (p.=)
c.397+8G>T (p.=)
c.940+8G>T (p.=)
c.166+8G>T (p.=)
ClinVar dbSNP

Number of alleles fetched