Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.150376328C>GCA3511103TCOF1c.2140C>G (p.Gln714Glu)
c.1909C>G (p.Gln637Glu)
c.1428C>G
n.940C>G
n.3394C>G
c.342+8411C>G (n.342+8411C>G)
n.2185C>G
n.2187C>G
dbSNP ExAC gnomAD v2
5g.150376328C>TCA16618140TCOF1c.2140C>T (p.Gln714Ter)
c.1909C>T (p.Gln637Ter)
c.1428C>T
n.940C>T
n.3394C>T
c.342+8411C>T (n.342+8411C>T)
n.2185C>T
n.2187C>T
ClinVar dbSNP

Number of alleles fetched