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Variant : CV90518 (NM_021257.3(NGB):c.276G>A (p.Leu92=)) Homo sapiens

Symbol: CV90518
Name: NM_021257.3(NGB):c.276G>A (p.Leu92=)
Condition: Malignant melanoma [RCV000070616]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: MIR1260A   NGB  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NC_000014.7:g.76804607C>T
NM_021257.3:c.276G>A
NC_000014.9:g.77268511C>T
NC_000014.8:g.77734854C>T
NR_031661.1:c.73+d2221C>T
NP_067080.1:p.Leu92=
Position
Human AssemblyChrPosition (strand)Source
GRCh381477,268,511 - 77,268,511CLINVAR
GRCh371477,734,854 - 77,734,854CLINVAR
Build 361476,804,607 - 76,804,607CLINVAR
Cytogenetic Map1414q24.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8635296
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.