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Variant : CV130037 (NM_139319.2(SLC17A8):c.101+10967A>G) Homo sapiens

Symbol: CV130037
Name: NM_139319.2(SLC17A8):c.101+10967A>G
Condition: Lung cancer [RCV000110524]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SLC17A8  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_139319.2:c.101+10967A>G
NG_021175.1:g.16381A>G
NC_000012.12:g.100368459A>G
NC_000012.11:g.100762237A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh3812100,368,459 - 100,368,459CLINVAR
GRCh3712100,762,237 - 100,762,237CLINVAR
Cytogenetic Map1212q23.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8653462
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.