List of variants in gene DDX41 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.465G>A (p.Met155Ile)	rs199697328	0.00031
NM_016222.4(DDX41):c.3G>A (p.Met1Ile)	rs141601766	0.00012
NM_016222.4(DDX41):c.1436G>A (p.Arg479Gln)	rs200307685	0.00010
NM_016222.4(DDX41):c.764G>A (p.Arg255His)	rs775735135	0.00002
NM_016222.4(DDX41):c.707C>T (p.Thr236Met)	rs747256985	0.00001
NM_016222.4(DDX41):c.798G>A (p.Ser266=)	rs750013130	0.00001
NM_016222.4(DDX41):c.1099-12C>A
NM_016222.4(DDX41):c.1549+3A>G
NM_016222.4(DDX41):c.305_306del (p.Lys102fs)	rs760059747
NM_016222.4(DDX41):c.445C>T (p.Pro149Ser)
NM_016222.4(DDX41):c.798+11C>T

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