Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.132921362C>ACA008101c.737+1G>T (p.=)
n.933+1G>T
c.584+1G>T (p.=)
c.374+1G>T (p.=)
c.737+1G>T
ClinVar dbSNP
9g.132921362C>TCA008095c.737+1G>A (p.=)
n.933+1G>A
c.584+1G>A (p.=)
c.374+1G>A (p.=)
c.737+1G>A
ClinVar dbSNP COSMIC

Number of alleles fetched