List of variants in gene NBN reported as uncertain significance for breast 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: 25

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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.1317A>G (p.Ile439Met)	rs28538230	0.00114
NM_002485.5(NBN):c.628G>T (p.Val210Phe)	rs61754796	0.00047
NM_002485.5(NBN):c.425A>G (p.Asn142Ser)	rs769414	0.00033
NM_002485.5(NBN):c.266G>C (p.Arg89Pro)	rs747315554	0.00014
NM_002485.5(NBN):c.456G>A (p.Met152Ile)	rs201816949	0.00014
NM_002485.5(NBN):c.1036G>A (p.Val346Met)	rs200297914	0.00011
NM_002485.5(NBN):c.-2C>T	rs202104448	0.00010
NM_002485.5(NBN):c.1398-10T>A	rs539960851	0.00006
NM_002485.5(NBN):c.278C>T (p.Ser93Leu)	rs12721593	0.00004
NM_002485.5(NBN):c.139G>A (p.Val47Met)	rs876658446	0.00003
NM_002485.5(NBN):c.702+9G>A	rs748373099	0.00003
NM_002485.5(NBN):c.1591A>G (p.Ile531Val)	rs587782330	0.00002
NM_002485.5(NBN):c.1667T>A (p.Val556Glu)	rs558023830	0.00002
NM_002485.5(NBN):c.1465C>G (p.Leu489Val)	rs143948240	0.00001
NM_002485.5(NBN):c.1754A>G (p.Glu585Gly)	rs763926389	0.00001
NM_002485.5(NBN):c.2196A>G (p.Gln732=)	rs587780780	0.00001
NM_002485.5(NBN):c.445C>T (p.His149Tyr)	rs1161054161	0.00001
NM_002485.5(NBN):c.798G>A (p.Pro266=)	rs368786672	0.00001
NM_002485.5(NBN):c.938C>T (p.Ala313Val)	rs730881862	0.00001
NM_002485.5(NBN):c.1264G>T (p.Ala422Ser)	rs1336243918
NM_002485.5(NBN):c.1516C>G (p.Gln506Glu)	rs876658535
NM_002485.5(NBN):c.1946T>C (p.Met649Thr)	rs1554556582
NM_002485.5(NBN):c.350CTT[1] (p.Ser118del)	rs730881841
NM_002485.5(NBN):c.832T>G (p.Ser278Ala)	rs1225178489

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