List of variants in gene MRE11 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.469A>G (p.Met157Val)	rs147771140	0.00006
NM_005591.4(MRE11):c.1508G>A (p.Arg503His)	rs774057024	0.00003
NM_005591.4(MRE11):c.572G>A (p.Arg191Gln)	rs746932208	0.00002
NM_005591.4(MRE11):c.1715G>A (p.Arg572Gln)	rs200085146	0.00001
NM_005591.4(MRE11):c.310A>T (p.Ser104Cys)	rs748434421	0.00001
NM_005591.4(MRE11):c.463C>T (p.Arg155Cys)	rs587782512	0.00001
NM_005591.4(MRE11):c.1567A>G (p.Met523Val)	rs1555005493
NM_005591.4(MRE11):c.1657C>G (p.Gln553Glu)	rs1945964376
NM_005591.4(MRE11):c.881T>C (p.Met294Thr)	rs1591692940
NM_005591.4(MRE11):c.890A>G (p.His297Arg)	rs762144883

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