Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.45967788G>ACA214980FYCO1c.1546C>T (p.Gln516Ter)
n.1761C>T
c.1426C>T (p.Gln476Ter)
c.1402C>T (p.Gln468Ter)
c.946C>T (p.Gln316Ter)
ClinVar dbSNP
3g.45967788G=CA1361904917FYCO1c.1546C= (p.Gln516=)
n.1761C=
c.1426C= (p.Gln476=)
c.1402C= (p.Gln468=)
c.946C= (p.Gln316=)
dbSNP

Number of alleles fetched