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)     

RNA change     

Protein     

P-domain     

Enzyme activity     

Predict-BioInf     

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     
+?/+? 14 c.2119G>T r.(?) p.(Asp707Tyr) EGF-like 3 - PolyphenII: probably damaging, 1, HumVar probably damaging, 0.980; SIFT: Not tolerated, SIFT2 Not tolerated; MutationTaster: disease causing; conservation: 0.914 (Ch, Rh, D, P, B, M, Ra, H, Rb, Ck, X, Z, S) ACGS likely pathogenic g.11231177G>T g.11120501G>T D686N - LDLR_001603 - PubMed: Alonso 2009 - - Germline - not in ExAC, September 2015 - - - Sarah Leigh
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