Details for LDLR:c.939C>A, p.Cys313Ter

CHROMOSOME 19
GENOMIC COORDINATES
hg19hg38
1121818911107513
VARIANT EFFECT nonsense
ANNOTATION FLAG automatically_attributed
GENE LDLR
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_000527.4
CDNA CHANGE c.939C>A
PROTEIN CHANGE p.Cys313Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.478926Disease causing
DBSNP ID rs13306512
1 combination linked to LDLR:c.939C>A, p.Cys313Ter OLI820
1 disease linked to LDLR:c.939C>A, p.Cys313Ter NON RARE IN EUROPE: Heterozygous familial hypercholesterolemia

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