List of variants in gene NBN reported as pathogenic for carcinoma

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.1071dup (p.Val358fs)	rs2129745554
NM_002485.5(NBN):c.1147G>T (p.Glu383Ter)	rs772909239
NM_002485.5(NBN):c.1502G>A (p.Trp501Ter)	rs1554558472
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650
NM_002485.5(NBN):c.966C>G (p.Tyr322Ter)	rs748453607

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