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Variant : CV87641 (NM_001001659.1(OR2A14):c.343G>A (p.Val115Met)) Homo sapiens

Symbol: CV87641
Name: NM_001001659.1(OR2A14):c.343G>A (p.Val115Met)
Condition: Malignant melanoma [RCV000067733]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR2A14  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_001001659.1:c.343G>A
NC_000007.14:g.144129455G>A
NC_000007.13:g.143826548G>A
NP_001001659.1:p.Val115Met
NC_000007.12:g.143457481G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh387144,129,455 - 144,129,455CLINVAR
GRCh377143,826,548 - 143,826,548CLINVAR
Build 367143,457,481 - 143,457,481CLINVAR
Cytogenetic Map77q35CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8632433
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.