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Variant : CV171651 (NM_024704.5(KIF16B):c.1979G>A (p.Arg660His)) Homo sapiens

Symbol: CV171651
Name: NM_024704.5(KIF16B):c.1979G>A (p.Arg660His)
Condition: Malignant tumor of prostate [RCV000149102]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: KIF16B  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NG_028043.1:g.198412G>A
NC_000020.11:g.16380023C>T
NC_000020.10:g.16360668C>T
NP_078980.3:p.Arg660His
NP_001186795.1:p.Arg660His
NM_001199866.2:c.1979G>A
NM_024704.5:c.1979G>A
NG_028043.2:g.198412G>A
NM_001199866.1:c.1979G>A
NP_001186794.1:p.Arg660His
NM_001199865.2:c.1979G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382016,380,023 - 16,380,023CLINVAR
GRCh372016,360,668 - 16,360,668CLINVAR
Cytogenetic Map2020p12.1CLINVAR
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
 
RGD Object Information
RGD ID: 9686884
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-07-21
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.