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Variant : CV403585 (NM_000527.4(LDLR):c.1562C>T (p.Ala521Val)) Homo sapiens

Symbol: CV403585
Name: NM_000527.4(LDLR):c.1562C>T (p.Ala521Val)
Condition: Familial hypercholesterolemia [RCV000475963]
Clinical Significance: uncertain significance
Last Evaluated: 10/22/2016
Review Status: criteria provided, single submitter
Related Genes: LDLR  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NP_001182732.1:p.Ala394Val
NP_001182728.1:p.Ala480Val
NP_001182727.1:p.Ala521Val
LRG_274t1:c.1562C>T
NM_000527.4:c.1562C>T
LRG_274:g.29358C>T
NG_009060.1:g.29358C>T
NC_000019.10:g.11113738C>T
NC_000019.9:g.11224414C>T
LRG_274p1:p.Ala521Val
NP_000518.1:p.Ala521Val
NM_001195800.2:c.1058C>T
NM_000527.4:c.1562C>T
NM_001195798.2:c.1562C>T
NP_001182729.1:p.Ala353Val
NM_001195803.2:c.1181C>T
NM_001195799.2:c.1439C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381911,113,738 - 11,113,738CLINVAR
GRCh371911,224,414 - 11,224,414CLINVAR
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
Prevalence: 1-9 / 1 000 000



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12891112
Created: 2017-05-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.