Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV171662 (NM_005560.5(LAMA5):c.2479C>T (p.Arg827Cys)) Homo sapiens

Symbol: CV171662
Name: NM_005560.5(LAMA5):c.2479C>T (p.Arg827Cys)
Condition: Malignant tumor of prostate [RCV000149172]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LAMA5  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NC_000020.11:g.62335024G>A
NC_000020.10:g.60910080G>A
NM_005560.3:c.2479C>T
NP_005551.3:p.Arg827Cys
NG_050626.1:g.37297C>T
NM_005560.5:c.2479C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh382062,335,024 - 62,335,024CLINVAR
GRCh372060,910,080 - 60,910,080CLINVAR
Cytogenetic Map2020q13.33CLINVAR
Trait Synonyms: Prostate cancer; Prostatic cancer
Age Of Onset: adulthood
Prevalence: 1-9 / 100 000



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9686953
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-10-15
Status: ACTIVE



NHLBI Logo

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