Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.43047705T>ACA003573BRCA1c.5407-2A>T (p.=)
c.5266-2A>T (p.=)
c.2095-2A>T (p.=)
c.2021-2A>T (p.=)
c.5470-2A>T (p.=)
n.5543-2A>T
c.1981-2A>T (p.=)
c.*5190-2A>T (p.=)
c.337-2A>T (p.=)
c.880-2A>T (p.=)
c.106-2A>T (p.=)
ClinVar dbSNP
17g.43047705T>CCA003572BRCA1c.5407-2A>G (p.=)
c.5266-2A>G (p.=)
c.2095-2A>G (p.=)
c.2021-2A>G (p.=)
c.5470-2A>G (p.=)
n.5543-2A>G
c.1981-2A>G (p.=)
c.*5190-2A>G (p.=)
c.337-2A>G (p.=)
c.880-2A>G (p.=)
c.106-2A>G (p.=)
ClinVar dbSNP

Number of alleles fetched