ClinVar Miner

List of variants in gene DDX39A reported as likely pathogenic by Department Of Translational Genomics (developmental Genetics Section), King Faisal Specialist Hospital & Research Centre

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_005804.4(DDX39A):c.677T>A (p.Phe226Tyr)	rs786205516

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