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Variant : CV171633 (NM_144685.5(HIPK4):c.1279G>A (p.Asp427Asn)) Homo sapiens

Symbol: CV171633
Name: NM_144685.5(HIPK4):c.1279G>A (p.Asp427Asn)
Condition: Malignant tumor of prostate [RCV000149343]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: HIPK4  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NC_000019.10:g.40380712C>T
NC_000019.9:g.40886619C>T
NM_144685.3:c.1279G>A
NP_653286.2:p.Asp427Asn
NG_051224.1:g.14510G>A
NM_144685.5:c.1279G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381940,380,712 - 40,380,712CLINVAR
GRCh371940,886,619 - 40,886,619CLINVAR
Cytogenetic Map1919q13.2CLINVAR
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
 
CRRD Object Information
CRRD ID: 9687124
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-10-15
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.