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Variant : CV89132 (NM_001005196.1(OR8B4):c.99G>A (p.Gly33=)) Homo sapiens

Symbol: CV89132
Name: NM_001005196.1(OR8B4):c.99G>A (p.Gly33=)
Condition: Malignant melanoma [RCV000069229]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR8B4  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001005196.1:c.99G>A
NC_000011.10:g.124424773C>T
NC_000011.9:g.124294669C>T
NP_001005196.1:p.Gly33=
NC_000011.8:g.123799879C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,424,773 - 124,424,773CLINVAR
GRCh3711124,294,669 - 124,294,669CLINVAR
Build 3611123,799,879 - 123,799,879CLINVAR
Cytogenetic Map1111q24.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633916
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.