List of variants in gene RAD50 reported as uncertain significance by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln)	rs146370443	0.00026
NM_005732.4(RAD50):c.1211A>G (p.Gln404Arg)	rs200017020	0.00009
NM_005732.4(RAD50):c.1924T>G (p.Leu642Val)	rs201132221	0.00001
NM_005732.4(RAD50):c.2209C>G (p.Gln737Glu)	rs549559726	0.00001
NM_005732.4(RAD50):c.2273A>G (p.Asn758Ser)	rs147568421	0.00001
NM_005732.4(RAD50):c.2287C>T (p.Arg763Cys)	rs369996457	0.00001
NM_005732.4(RAD50):c.3380C>T (p.Thr1127Ile)	rs1395170959	0.00001
NM_005732.4(RAD50):c.353T>C (p.Ile118Thr)	rs200472836	0.00001
NM_005732.4(RAD50):c.1831A>G (p.Ile611Val)	rs138315079
NM_005732.4(RAD50):c.2603A>G (p.Asn868Ser)	rs758941378
NM_005732.4(RAD50):c.547A>G (p.Thr183Ala)	rs1029393718

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