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Variant : CV90365 (NM_001004712.1(OR4K14):c.880G>A (p.Glu294Lys)) Homo sapiens

Symbol: CV90365
Name: NM_001004712.1(OR4K14):c.880G>A (p.Glu294Lys)
Condition: Malignant melanoma [RCV000070463]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR4K14  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_001004712.1:c.880G>A
NC_000014.9:g.20014314C>T
NC_000014.8:g.20482473C>T
NP_001004712.1:p.Glu294Lys
NC_000014.7:g.19552313C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381420,014,314 - 20,014,314CLINVAR
GRCh371420,482,473 - 20,482,473CLINVAR
Build 361419,552,313 - 19,552,313CLINVAR
Cytogenetic Map1414q11.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8635143
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.