List of variants in gene RAD21 studied for not specified

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_006265.3(RAD21):c.1440T>C (p.Ala480=)	rs1050838	0.13625
NM_006265.3(RAD21):c.688+8G>A	rs2921787	0.11506
NM_006265.3(RAD21):c.938-11T>C	rs200333487	0.00399
NM_006265.3(RAD21):c.-32-1G>A	rs16889042	0.00125
NM_006265.3(RAD21):c.735C>T (p.Pro245=)	rs199767556	0.00029
NM_006265.3(RAD21):c.1185G>A (p.Pro395=)	rs138247094	0.00026
NM_006265.3(RAD21):c.93T>C (p.His31=)	rs761516272	0.00002
NM_006265.3(RAD21):c.-51A>T	rs16889189
NM_006265.3(RAD21):c.1162-6del	rs369816312
NM_006265.3(RAD21):c.1252A>C (p.Lys418Gln)	rs1812375108
NM_006265.3(RAD21):c.1348C>T (p.Arg450Cys)
NM_006265.3(RAD21):c.1454C>G (p.Pro485Arg)
NM_006265.3(RAD21):c.1895A>G (p.Ter632=)	rs1315026169
NM_006265.3(RAD21):c.269G>A (p.Arg90Gln)	rs1554612086
NM_006265.3(RAD21):c.785A>T (p.Asp262Val)	rs2130467945
NM_006265.3(RAD21):c.815-6_815-5del	rs35902828

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