Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.55957191C>GCA6620069PMELc.1112G>C (p.Ser371Thr)
c.950G>C (p.Ser317Thr)
c.665G>C (p.Ser222Thr)
c.774G>C
n.152G>C
c.358+1282G>C (n.358+1282G>C)
c.854G>C (p.Ser285Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.55957191C>TCA385217271PMELc.1112G>A (p.Ser371Asn)
c.950G>A (p.Ser317Asn)
c.665G>A (p.Ser222Asn)
c.774G>A
n.152G>A
c.358+1282G>A (n.358+1282G>A)
c.854G>A (p.Ser285Asn)
dbSNP gnomAD v2 gnomAD v4
12g.55957191C=CA2038181288PMELc.1112G= (p.Ser371=)
c.950G= (p.Ser317=)
c.665G= (p.Ser222=)
c.774G=
n.152G=
c.358+1282G= (n.358+1282G=)
c.854G= (p.Ser285=)
dbSNP

Number of alleles fetched