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Variant : CV120543 (NM_001130065.1(MYO9B):c.840+18695T>G) Homo sapiens

Symbol: CV120543
Name: NM_001130065.1(MYO9B):c.840+18695T>G
Condition: Lung cancer [RCV000101063]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MYO9B  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_001130065.1:c.840+18695T>G
NG_013068.1:g.50472T>G
NC_000019.10:g.17121252T>G
NC_000019.9:g.17232062T>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381917,121,252 - 17,121,252CLINVAR
GRCh371917,232,062 - 17,232,062CLINVAR
Cytogenetic Map1919p13.11CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8585948
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.