Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.11105517G>TCA10585012LDLRc.869G>T (p.Cys290Phe)
c.611G>T (p.Cys204Phe)
c.865G>T
c.314-1875G>T (n.314-1875G>T)
c.488G>T (p.Cys163Phe)
c.314-1048G>T (n.314-1048G>T)
c.211G>T
n.761G>T
n.728G>T
ClinVar dbSNP
19g.11105517G>CCA10585011LDLRc.869G>C (p.Cys290Ser)
c.611G>C (p.Cys204Ser)
c.865G>C
c.314-1875G>C (n.314-1875G>C)
c.488G>C (p.Cys163Ser)
c.314-1048G>C (n.314-1048G>C)
c.211G>C
n.761G>C
n.728G>C
ClinVar dbSNP
19g.11105517G>ACA10585010LDLRc.869G>A (p.Cys290Tyr)
c.611G>A (p.Cys204Tyr)
c.865G>A
c.314-1875G>A (n.314-1875G>A)
c.488G>A (p.Cys163Tyr)
c.314-1048G>A (n.314-1048G>A)
c.211G>A
n.761G>A
n.728G>A
ClinVar dbSNP

Number of alleles fetched