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Variant : CV89131 (NM_001002918.1(OR8D2):c.642C>T (p.Val214=)) Homo sapiens

Symbol: CV89131
Name: NM_001002918.1(OR8D2):c.642C>T (p.Val214=)
Condition: Malignant melanoma [RCV000069228]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR8D2   OR8G5  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001002918.1:c.642C>T
NC_000011.10:g.124319556G>A
NC_000011.9:g.124189452G>A
NP_001002918.1:p.Val214=
NC_000011.8:g.123694662G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,319,556 - 124,319,556CLINVAR
GRCh3711124,189,452 - 124,189,452CLINVAR
Build 3611123,694,662 - 123,694,662CLINVAR
Cytogenetic Map1111q24.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633915
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.