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Variant : CV81861 (NM_022343.3(GLIPR2):c.149G>C (p.Arg50Thr)) Homo sapiens

Symbol: CV81861
Name: NM_022343.3(GLIPR2):c.149G>C (p.Arg50Thr)
Condition: Malignant melanoma [RCV000061940]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: GLIPR2  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant|missense variant|non-coding transcript variant
Evidence: literature only|not provided
HGVS Name(s): NC_000009.10:g.36138570G>C
NC_000009.12:g.36148573G>C
NC_000009.11:g.36148570G>C
NP_071738.1:p.Arg50Thr
NM_022343.3:c.149G>C
NM_022343.2:c.149G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh38936,148,573 - 36,148,573CLINVAR
GRCh37936,148,570 - 36,148,570CLINVAR
Build 36936,138,570 - 36,138,570CLINVAR
Cytogenetic Map99p13.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8626717
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.