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Variant : CV171588 (NM_014683.4(ULK2):c.514G>T (p.Ala172Ser)) Homo sapiens

Symbol: CV171588
Name: NM_014683.4(ULK2):c.514G>T (p.Ala172Ser)
Condition: Malignant tumor of prostate [RCV000149217]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ULK2  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NC_000017.11:g.19845333C>A
NC_000017.10:g.19748646C>A
NP_055498.3:p.Ala172Ser
NG_047113.1:g.27594G>T
NM_001142610.2:c.514G>T
NM_014683.4:c.514G>T
NM_014683.3:c.514G>T
NP_001136082.1:p.Ala172Ser
Position
Human AssemblyChrPosition (strand)Source
GRCh381719,845,333 - 19,845,333CLINVAR
GRCh371719,748,646 - 19,748,646CLINVAR
Cytogenetic Map1717p11.2CLINVAR
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
 
RGD Object Information
RGD ID: 9686998
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-09-22
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.