List of variants in gene NBN reported as pathogenic for Breast and/or ovarian cancer

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.37+1G>A	rs574673404	0.00002
NM_002485.5(NBN):c.1393A>T (p.Lys465Ter)	rs1563530658
NM_002485.5(NBN):c.1645A>T (p.Lys549Ter)	rs1810540992
NM_002485.5(NBN):c.188del (p.Ile63fs)	rs876659592
NM_002485.5(NBN):c.5G>A (p.Trp2Ter)	rs1812244679
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650

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