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Variant : CV85383 (NM_005683.3(GPR55):c.93C>T (p.Phe31=)) Homo sapiens

Symbol: CV85383
Name: NM_005683.3(GPR55):c.93C>T (p.Phe31=)
Condition: Malignant melanoma [RCV000065465]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: GPR55  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_005683.3:c.93C>T
NC_000002.12:g.230910870G>A
NC_000002.11:g.231775585G>A
NP_005674.2:p.Phe31=
NC_000002.10:g.231483829G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382230,910,870 - 230,910,870CLINVAR
GRCh372231,775,585 - 231,775,585CLINVAR
Build 362231,483,829 - 231,483,829CLINVAR
Cytogenetic Map22q37.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8630236
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.