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Variant : CV434204 (NM_000527.4(LDLR):c.263G>A (p.Arg88Lys)) Homo sapiens

Symbol: CV434204
Name: NM_000527.4(LDLR):c.263G>A (p.Arg88Lys)
Condition: Familial hypercholesterolemia [RCV000508713]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: LDLR  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: research
HGVS Name(s): LRG_274t1:c.263G>A
LRG_274:g.18356G>A
NG_009060.1:g.18356G>A
NC_000019.10:g.11102736G>A
NC_000019.9:g.11213412G>A
LRG_274p1:p.Arg88Lys
NP_000518.1:p.Arg88Lys
NM_001195799.2:c.190+2391G>A
NM_001195798.2:c.263G>A
NM_001195800.2:c.263G>A
NM_001195803.2:c.263G>A
NP_001182727.1:p.Arg88Lys
NP_001182729.1:p.Arg88Lys
NP_001182732.1:p.Arg88Lys
Position
Human AssemblyChrPosition (strand)Source
GRCh381911,102,736 - 11,102,736CLINVAR
GRCh371911,213,412 - 11,213,412CLINVAR
Cytogenetic Map1919p13.2CLINVAR
Trait Synonyms: Fredrickson type IIa hyperlipoproteinemia; HYPER-LOW-DENSITY-LIPOPROTEINEMIA; HYPERCHOLESTEROLEMIA, FAMILIAL, 1; HYPERCHOLESTEROLEMIA, FAMILIAL, MODIFIER OF; HYPERCHOLESTEROLEMIC XANTHOMATOSIS, FAMILIAL; Hyperlipoproteinemia Type II; Hyperlipoproteinemia Type IIa; LDL RECEPTOR DISORDER



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13437350
Created: 2017-10-10
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.