All variants in the LDLR gene

Information The variants shown are described using the NM_000527.4 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

Protein     

RNA change     

DNA/Legacy     

Predict/MutationTaster     

P-domain     

Predict/PolyPhen     

Predict/SIFT     

Conservation     

Predict/Splice     

Enzyme activity     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+?/+? 13 c.1855T>C p.(Phe619Leu) r.(?) F598L disease causing LDL-receptor class B6 PPII HumDiv benign, 0.401; HumVar possibly damaging, 0.773 Not tolerated; SIFT2 Not tolerated 0.812; (Ch, Rh, D, P, B, H, Rb, Ck, X, Z, S) - - ACGS likely pathogenic g.11230777T>C g.11120101T>C - - LDLR_000570 - PubMed: Sun 1997 - - Germline - not in ExAC, May 2015 - 0 - Sarah Leigh
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