List of variants in gene NBN studied for breast carcinoma

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.511A>G (p.Ile171Val)	rs61754966	0.00145
NM_002485.5(NBN):c.1262T>C (p.Leu421Ser)	rs104895032	0.00027
NM_002485.5(NBN):c.445C>T (p.His149Tyr)	rs1161054161	0.00001
NM_002485.5(NBN):c.1154_1155del (p.Lys385fs)	rs748513310
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.93_94del (p.Ala32fs)	rs864622253
NM_002485.5(NBN):c.966C>G (p.Tyr322Ter)	rs748453607

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