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Variant : CV109892 (NM_172362.2(KCNH1):c.558+6849G>T) Homo sapiens

Symbol: CV109892
Name: NM_172362.2(KCNH1):c.558+6849G>T
Condition: Lung cancer [RCV000090417]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: KCNH1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_172362.2:c.558+6849G>T
NG_029777.1:g.63185G>T
NC_000001.11:g.211075931C>A
NC_000001.10:g.211249273C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381211,075,931 - 211,075,931CLINVAR
GRCh371211,249,273 - 211,249,273CLINVAR
Cytogenetic Map11q32.2CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8575544
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.