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Variant : CV590921 (NM_005560.5(LAMA5):c.6101A>G (p.Asp2034Gly)) Homo sapiens

Symbol: CV590921
Name: NM_005560.5(LAMA5):c.6101A>G (p.Asp2034Gly)
Condition: Short stature [RCV000736126]
Clinical Significance: likely pathogenic
Last Evaluated: 11/18/2001
Review Status: no assertion criteria provided
Related Genes: LAMA5  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: case-control
HGVS Name(s): NM_005560.5:c.6101A>G
NG_050626.1:g.49599A>G
NC_000020.11:g.62322722T>C
NM_005560.4:c.6101A>G
NP_005551.3:p.Asp2034Gly
NC_000020.10:g.60897778T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh382062,322,722 - 62,322,722CLINVAR
GRCh372060,897,778 - 60,897,778CLINVAR
Cytogenetic Map2020q13.33CLINVAR
Trait Synonyms: Decreased body height; Height less than 3rd percentile; Small stature; Stature below 3rd percentile



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14349930
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-10-20
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.