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

Variant : CV80081 (NM_001004691.1(OR2M7):c.516G>A (p.Arg172=)) Homo sapiens

Symbol: CV80081
Name: NM_001004691.1(OR2M7):c.516G>A (p.Arg172=)
Condition: Malignant melanoma [RCV000060157]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OR2M7  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001004691.1:c.516G>A
NC_000001.11:g.248324053C>T
NC_000001.10:g.248487355C>T
NP_001004691.1:p.Arg172=
NC_000001.9:g.246553978C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381248,324,053 - 248,324,053CLINVAR
GRCh371248,487,355 - 248,487,355CLINVAR
Build 361246,553,978 - 246,553,978CLINVAR
Cytogenetic Map11q44CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8624962
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.