List of variants in gene DDX41 reported as pathogenic by Baylor Genetics

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)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.415_418dup (p.Asp140delinsGlyTer)	rs762890562	0.00007
NM_016222.4(DDX41):c.142C>T (p.Gln48Ter)	rs377745714	0.00005
NM_016222.4(DDX41):c.121C>T (p.Gln41Ter)	rs746278774	0.00001
NM_016222.4(DDX41):c.475C>T (p.Arg159Ter)	rs754907965	0.00001
NM_016222.4(DDX41):c.931C>T (p.Arg311Ter)	rs899399494	0.00001
NM_016222.4(DDX41):c.946_947del (p.Met316fs)	rs1411544367	0.00001
NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs)	rs866179648
NM_016222.4(DDX41):c.434+1G>C	rs1170971274
NM_016222.4(DDX41):c.847del (p.Leu283fs)	rs1761145210

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