List of variants in gene LIG4 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_206937.2(LIG4):c.2525C>A (p.Ala842Asp)	rs72660870	0.00129
NM_206937.2(LIG4):c.691C>T (p.Pro231Ser)	rs3093765	0.00048
NM_206937.2(LIG4):c.1705A>G (p.Met569Val)	rs774699419	0.00011
NM_206937.2(LIG4):c.2440C>T (p.Arg814Ter)	rs104894419	0.00007
NM_206937.2(LIG4):c.1882C>T (p.Arg628Trp)	rs755708095	0.00005
NM_206937.2(LIG4):c.381G>C (p.Met127Ile)	rs61752350	0.00005
NM_206937.2(LIG4):c.524T>C (p.Ile175Thr)	rs373262036	0.00001
NM_206937.2(LIG4):c.560T>C (p.Ile187Thr)	rs199854013	0.00001
NM_206937.2(LIG4):c.1271_1275del (p.Lys424fs)	rs772226399
NM_206937.2(LIG4):c.1704_1705delinsCG (p.Met569Val)	rs1878367870

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