Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.11105289G>TCA10584893LDLRc.641G>T (p.Cys214Phe)
c.383G>T (p.Cys128Phe)
c.637G>T
c.314-2103G>T (n.314-2103G>T)
c.260G>T (p.Cys87Phe)
c.314-1276G>T (n.314-1276G>T)
n.533G>T
n.500G>T
ClinVar dbSNP
19g.11105289G>CCA16609803LDLRc.641G>C (p.Cys214Ser)
c.383G>C (p.Cys128Ser)
c.637G>C
c.314-2103G>C (n.314-2103G>C)
c.260G>C (p.Cys87Ser)
c.314-1276G>C (n.314-1276G>C)
n.533G>C
n.500G>C
ClinVar dbSNP
19g.11105289G>ACA16602299LDLRc.641G>A (p.Cys214Tyr)
c.383G>A (p.Cys128Tyr)
c.637G>A
c.314-2103G>A (n.314-2103G>A)
c.260G>A (p.Cys87Tyr)
c.314-1276G>A (n.314-1276G>A)
n.533G>A
n.500G>A
ClinVar dbSNP

Number of alleles fetched