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Variant : CV86919 (NM_020546.2(ADCY2):c.2582C>T (p.Pro861Leu)) Homo sapiens

Symbol: CV86919
Name: NM_020546.2(ADCY2):c.2582C>T (p.Pro861Leu)
Condition: Malignant melanoma [RCV000067010]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: ADCY2  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_020546.2:c.2582C>T
NC_000005.10:g.7789754C>T
NC_000005.9:g.7789867C>T
NP_065433.2:p.Pro861Leu
NC_000005.8:g.7842867C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3857,789,754 - 7,789,754CLINVAR
GRCh3757,789,867 - 7,789,867CLINVAR
Build 3657,842,867 - 7,842,867CLINVAR
Cytogenetic Map55p15.31CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8631713
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.