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Variant : CV90595 (NM_001005241.3(OR4N4):c.462C>T (p.Val154=)) Homo sapiens

Symbol: CV90595
Name: NM_001005241.3(OR4N4):c.462C>T (p.Val154=)
Condition: Malignant melanoma [RCV000070693]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR4N4  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: synonymous variant|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000015.10:g.22094983C>T
NC_000015.9:g.22382934C>T
NM_001005241.1:c.462C>T
NP_001005241.2:p.Val154=
NM_001005241.3:c.462C>T
NM_001005241.2:c.462C>T
NC_000015.8:g.19884298C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381522,094,983 - 22,094,983CLINVAR
GRCh371522,382,934 - 22,382,934CLINVAR
Build 361519,884,298 - 19,884,298CLINVAR
Cytogenetic Map1515q11.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8635373
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.