List of variants in gene RAD50 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.1534G>T (p.Ala512Ser)	rs147366706	0.00079
NM_005732.4(RAD50):c.3036+5G>A	rs181016343	0.00078
NM_005732.4(RAD50):c.260G>A (p.Arg87His)	rs374561375	0.00042
NM_005732.4(RAD50):c.2397G>C (p.Gln799His)	rs61749630	0.00036
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln)	rs146370443	0.00026
NM_005732.4(RAD50):c.2288G>A (p.Arg763His)	rs141989813	0.00026
NM_005732.4(RAD50):c.2177G>A (p.Arg726His)	rs28903092	0.00025
NM_005732.4(RAD50):c.1336A>G (p.Lys446Glu)	rs149217423	0.00024
NM_005732.4(RAD50):c.1677C>T (p.His559=)	rs142619269	0.00022
NM_005732.4(RAD50):c.2525T>C (p.Val842Ala)	rs28903093	0.00020
NM_005732.4(RAD50):c.1277A>G (p.Gln426Arg)	rs145428112	0.00015
NM_005732.4(RAD50):c.2688T>C (p.Thr896=)	rs537257801	0.00015
NM_005732.4(RAD50):c.2548C>T (p.Arg850Cys)	rs181961360	0.00010
NM_005732.4(RAD50):c.1911T>A (p.Asp637Glu)	rs144749616	0.00007
NM_005732.4(RAD50):c.130-10A>G	rs200760698	0.00006
NM_005732.4(RAD50):c.1663A>G (p.Ile555Val)	rs201120953	0.00006
NM_005732.4(RAD50):c.2173C>T (p.Arg725Trp)	rs369560280	0.00006
NM_005732.4(RAD50):c.610A>G (p.Lys204Glu)	rs202197835	0.00006
NM_005732.4(RAD50):c.2445G>A (p.Lys815=)	rs183510397	0.00002
NM_005732.4(RAD50):c.1605T>C (p.Arg535=)	rs878854785	0.00001
NM_005732.4(RAD50):c.2209C>G (p.Gln737Glu)	rs549559726	0.00001
NM_005732.4(RAD50):c.2409A>G (p.Lys803=)	rs762456674	0.00001
NM_005732.4(RAD50):c.2468G>A (p.Arg823Gln)	rs572533256	0.00001
NM_005732.4(RAD50):c.2472T>G (p.Thr824=)	rs1358470664	0.00001
NM_005732.4(RAD50):c.2530A>C (p.Ser844Arg)	rs373817937	0.00001
NM_005732.4(RAD50):c.323A>G (p.Lys108Arg)	rs542347773	0.00001
NM_005732.4(RAD50):c.353T>C (p.Ile118Thr)	rs200472836	0.00001
NM_005732.4(RAD50):c.927C>T (p.His309=)	rs758239327	0.00001
NM_005732.4(RAD50):c.1311T>C (p.Thr437=)	rs786202706
NM_005732.4(RAD50):c.1689A>G (p.Leu563=)	rs1580994836
NM_005732.4(RAD50):c.1875C>T (p.Tyr625=)	rs149201802
NM_005732.4(RAD50):c.2655G>A (p.Gln885=)	rs1554099195
NM_005732.4(RAD50):c.36G>A (p.Val12=)	rs1580974379

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