List of variants in gene XRCC4 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003401.5(XRCC4):c.224T>C (p.Leu75Ser)	rs61762970	0.00128
NM_003401.5(XRCC4):c.166G>A (p.Ala56Thr)	rs28383151	0.00051
NM_003401.5(XRCC4):c.894-13T>G	rs369970969	0.00027
NM_003401.5(XRCC4):c.139+7C>T	rs373131654	0.00026
NM_003401.5(XRCC4):c.483-15T>G	rs199551802	0.00024
NM_003401.5(XRCC4):c.140-15T>C	rs375480555	0.00022
NM_003401.5(XRCC4):c.970A>C (p.Asn324His)	rs61749611	0.00019
NM_003401.5(XRCC4):c.140-4A>G	rs143971157	0.00011
NM_003401.5(XRCC4):c.640G>A (p.Glu214Lys)	rs746407658	0.00006
NM_003401.5(XRCC4):c.80C>T (p.Thr27Ile)	rs550773308	0.00006
NM_003401.5(XRCC4):c.943G>A (p.Glu315Lys)	rs780229187	0.00002
NM_003401.5(XRCC4):c.458G>A (p.Arg153Lys)	rs1277864722	0.00001
NM_003401.5(XRCC4):c.628A>T (p.Lys210Ter)	rs991596636	0.00001
NM_003401.5(XRCC4):c.25del (p.His9fs)	rs869320677
NM_003401.5(XRCC4):c.265del (p.Ser89fs)	rs772562216
NM_003401.5(XRCC4):c.356C>T (p.Pro119Leu)	rs768175717

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