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Variant : CV118437 (NM_002788.3(PSMA3):c.544-13T>G) Homo sapiens

Symbol: CV118437
Name: NM_002788.3(PSMA3):c.544-13T>G
Condition: Lung cancer [RCV000098957]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PSMA3   PSMA3-AS1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000014.9:g.58267461T>G
NC_000014.8:g.58734179T>G
NM_002788.3:c.544-13T>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381458,267,461 - 58,267,461CLINVAR
GRCh371458,734,179 - 58,734,179CLINVAR
Cytogenetic Map1414q23.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8583870
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.