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Variant : CV82085 (NM_001002917.1(OR8D1):c.886G>A (p.Asp296Asn)) Homo sapiens

Symbol: CV82085
Name: NM_001002917.1(OR8D1):c.886G>A (p.Asp296Asn)
Condition: Malignant melanoma [RCV000062164]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR8D1   OR8G5  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_001002917.1:c.886G>A
NC_000011.10:g.124309881C>T
NC_000011.9:g.124179777C>T
NP_001002917.1:p.Asp296Asn
NC_000011.8:g.123684987C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,309,881 - 124,309,881CLINVAR
GRCh3711124,179,777 - 124,179,777CLINVAR
Build 3611123,684,987 - 123,684,987CLINVAR
Cytogenetic Map1111q24.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8626941
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
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.