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Variant : CV171495 (NM_020809.3(ARHGAP20):c.464T>C (p.Val155Ala)) Homo sapiens

Symbol: CV171495
Name: NM_020809.3(ARHGAP20):c.464T>C (p.Val155Ala)
Condition: Malignant tumor of prostate [RCV000149273]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP20  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NM_020809.3:c.464T>C
NC_000011.10:g.110624201A>G
NC_000011.9:g.110494925A>G
NM_020809.2:c.464T>C
NP_065860.2:p.Val155Ala
NP_001245346.1:p.Val119Ala
NP_001245347.1:p.Val119Ala
NP_001245345.1:p.Val129Ala
NP_001245344.1:p.Val132Ala
NG_051657.1:g.93989T>C
NM_001258417.1:c.356T>C
NM_001258418.1:c.356T>C
NM_001258416.1:c.386T>C
NM_001258415.2:c.395T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh3811110,624,201 - 110,624,201CLINVAR
GRCh3711110,494,925 - 110,494,925CLINVAR
Cytogenetic Map1111q23.1CLINVAR
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: 9687054
Created: 2015-02-10
Species: Homo sapiens
Last Modified: 2020-05-19
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.