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Variant : CV115665 (NM_020546.2(ADCY2):c.2628+1827T>A) Homo sapiens

Symbol: CV115665
Name: NM_020546.2(ADCY2):c.2628+1827T>A
Condition: Lung cancer [RCV000096188]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADCY2  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000005.10:g.7791627T>A
NC_000005.9:g.7791740T>A
NM_020546.2:c.2628+1827T>A
Position
Human AssemblyChrPosition (strand)Source
GRCh3857,791,627 - 7,791,627CLINVAR
GRCh3757,791,740 - 7,791,740CLINVAR
Cytogenetic Map55p15.31CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8581228
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.