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Variant : CV246064 (NM_000527.4(LDLR):c.1244A>T (p.Asp415Val)) Homo sapiens

Symbol: CV246064
Name: NM_000527.4(LDLR):c.1244A>T (p.Asp415Val)
Condition: Familial hypercholesterolemia [RCV000237518]
Clinical Significance: uncertain significance
Last Evaluated: 03/25/2016
Review Status: criteria provided, single submitter
Related Genes: LDLR  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): LRG_274t1:c.1244A>T
NM_000527.4:c.1244A>T
LRG_274:g.28955A>T
NG_009060.1:g.28955A>T
NC_000019.10:g.11113335A>T
NC_000019.9:g.11224011A>T
c.1244A>T
LRG_274p1:p.Asp415Val
NP_000518.1:p.Asp415Val
NM_001195803.2:c.863A>T
NP_001182729.1:p.Asp247Val
NP_001182732.1:p.Asp288Val
NP_001182728.1:p.Asp374Val
NM_001195799.2:c.1121A>T
NM_001195798.2:c.1244A>T
NM_001195800.2:c.740A>T
NP_001182727.1:p.Asp415Val
Position
Human AssemblyChrPosition (strand)Source
GRCh381911,113,335 - 11,113,335CLINVAR
GRCh371911,224,011 - 11,224,011CLINVAR
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: 11524518
Created: 2016-08-09
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.