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Variant : CV129109 (NM_001258415.1(ARHGAP20):c.896-6231C>T) Homo sapiens

Symbol: CV129109
Name: NM_001258415.1(ARHGAP20):c.896-6231C>T
Condition: Lung cancer [RCV000109596]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP20  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000011.10:g.110598386G>A
NC_000011.9:g.110469110G>A
NM_001258415.1:c.896-6231C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3811110,598,386 - 110,598,386CLINVAR
GRCh3711110,469,110 - 110,469,110CLINVAR
Cytogenetic Map1111q22.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8652534
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.