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Variant : CV89128 (NM_001002905.1(OR8G1):c.855G>A (p.Leu285=)) Homo sapiens

Symbol: CV89128
Name: NM_001002905.1(OR8G1):c.855G>A (p.Leu285=)
Condition: Malignant melanoma [RCV000069225]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR8G1   OR8G5  
Variant Type: single nucleotide variant (SO:0001619)
Source: CLINVAR
Molecular Consequence: synonymous variant|non-coding transcript variant
Evidence: literature only|not provided
HGVS Name(s): NM_001002905.1:c.855G>A
NC_000011.10:g.124250530G>A
NC_000011.9:g.124121277G>A
NC_000011.8:g.123626487G>A
NP_001002905.1:p.Leu285=
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,250,530 - 124,250,530CLINVAR
GRCh3711124,121,277 - 124,121,277CLINVAR
Build 3611123,626,487 - 123,626,487CLINVAR
Cytogenetic Map1111q24.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633912
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.