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Variant : CV171343 (NM_005683.4(GPR55):c.941C>T (p.Thr314Ile)) Homo sapiens

Symbol: CV171343
Name: NM_005683.4(GPR55):c.941C>T (p.Thr314Ile)
Condition: Malignant tumor of prostate [RCV000149174]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GPR55  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NC_000002.12:g.230910022G>A
NC_000002.11:g.231774737G>A
NP_005674.2:p.Thr314Ile
NG_050956.1:g.56206C>T
NM_005683.4:c.941C>T
NM_005683.3:c.941C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh382230,910,022 - 230,910,022CLINVAR
GRCh372231,774,737 - 231,774,737CLINVAR
Cytogenetic Map22q37.1CLINVAR
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: 9686955
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-02-11
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.