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Variant : CV88273 (NM_033105.4(DNAJC5B):c.499G>A (p.Glu167Lys)) Homo sapiens

Symbol: CV88273
Name: NM_033105.4(DNAJC5B):c.499G>A (p.Glu167Lys)
Condition: Malignant melanoma [RCV000068365]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: DNAJC5B  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_033105.4:c.499G>A
NC_000008.11:g.66080542G>A
NC_000008.10:g.66992777G>A
NP_149096.2:p.Glu167Lys
NC_000008.9:g.67155331G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38866,080,542 - 66,080,542CLINVAR
GRCh37866,992,777 - 66,992,777CLINVAR
Build 36867,155,331 - 67,155,331CLINVAR
Cytogenetic Map88q13.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633059
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.