Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.67752520G>ACA358160ZFYVE26c.7195C>T (p.Gln2399Ter)
c.7213C>T (p.Gln2405Ter)
c.7117C>T (p.Gln2373Ter)
c.7240C>T (p.Gln2414Ter)
n.2458C>T
n.7950C>T
c.*5173C>T (n.*5173C>T)
c.733C>T (p.Gln245Ter)
c.5686C>T (p.Gln1896Ter)
c.4870C>T (p.Gln1624Ter)
c.4777C>T (p.Gln1593Ter)
c.5704C>T (p.Gln1902Ter)
c.4888C>T (p.Gln1630Ter)
c.4795C>T (p.Gln1599Ter)
ClinVar dbSNP
14g.67752520G=CA2144014401ZFYVE26c.7195C= (p.Gln2399=)
c.7213C= (p.Gln2405=)
c.7117C= (p.Gln2373=)
c.7240C= (p.Gln2414=)
n.2458C=
n.7950C=
c.*5173C= (n.*5173C=)
c.733C= (p.Gln245=)
c.5686C= (p.Gln1896=)
c.4870C= (p.Gln1624=)
c.4777C= (p.Gln1593=)
c.5704C= (p.Gln1902=)
c.4888C= (p.Gln1630=)
c.4795C= (p.Gln1599=)
dbSNP

Number of alleles fetched