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Variant : CV87640 (NM_001001659.1(OR2A14):c.246G>A (p.Thr82=)) Homo sapiens

Symbol: CV87640
Name: NM_001001659.1(OR2A14):c.246G>A (p.Thr82=)
Condition: Malignant melanoma [RCV000067732]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR2A14  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001001659.1:c.246G>A
NC_000007.14:g.144129358G>A
NC_000007.13:g.143826451G>A
NP_001001659.1:p.Thr82=
NC_000007.12:g.143457384G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh387144,129,358 - 144,129,358CLINVAR
GRCh377143,826,451 - 143,826,451CLINVAR
Build 367143,457,384 - 143,457,384CLINVAR
Cytogenetic Map77q35CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8632432
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.