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

Variant : CV171652 (NM_024704.5(KIF16B):c.1588G>A (p.Val530Met)) Homo sapiens

Symbol: CV171652
Name: NM_024704.5(KIF16B):c.1588G>A (p.Val530Met)
Condition: Malignant tumor of prostate [RCV000149101]
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.151307G>A
NC_000020.11:g.16427128C>T
NC_000020.10:g.16407773C>T
NP_078980.3:p.Val530Met
NP_001186795.1:p.Val530Met
NM_001199865.2:c.1588G>A
NG_028043.2:g.151307G>A
NM_001199866.1:c.1588G>A
NP_001186794.1:p.Val530Met
NM_001199866.2:c.1588G>A
NM_024704.5:c.1588G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382016,427,128 - 16,427,128CLINVAR
GRCh372016,407,773 - 16,407,773CLINVAR
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: 9686883
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-07-21
Status: ACTIVE



NHLBI Logo

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