Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV89295 (NM_001004727.1(OR4X2):c.660G>A (p.Trp220Ter)) Homo sapiens

Symbol: CV89295
Name: NM_001004727.1(OR4X2):c.660G>A (p.Trp220Ter)
Condition: Malignant melanoma [RCV000069392]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR4X2  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: stop-gain|nonsense
Evidence: literature only|not provided
HGVS Name(s): NM_001004727.1:c.660G>A
NC_000011.10:g.48245763G>A
NC_000011.9:g.48267315G>A
NP_001004727.1:p.Trp220Ter
NC_000011.8:g.48223891G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381148,245,763 - 48,245,763CLINVAR
GRCh371148,267,315 - 48,267,315CLINVAR
Build 361148,223,891 - 48,223,891CLINVAR
Cytogenetic Map1111p11.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8634077
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.