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Variant : CV89130 (NM_001002917.1(OR8D1):c.204C>T (p.Phe68=)) Homo sapiens

Symbol: CV89130
Name: NM_001002917.1(OR8D1):c.204C>T (p.Phe68=)
Condition: Malignant melanoma [RCV000069227]
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:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001002917.1:c.204C>T
NC_000011.10:g.124310563G>A
NC_000011.9:g.124180459G>A
NP_001002917.1:p.Phe68=
NC_000011.8:g.123685669G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,310,563 - 124,310,563CLINVAR
GRCh3711124,180,459 - 124,180,459CLINVAR
Build 3611123,685,669 - 123,685,669CLINVAR
Cytogenetic Map1111q24.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633914
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.