List of variants in gene NBN reported as not provided

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.553G>C (p.Glu185Gln)	rs1805794	0.30329
NM_002485.5(NBN):c.703-29C>T	rs104895034	0.01266
NM_002485.5(NBN):c.797C>T (p.Pro266Leu)	rs769420	0.00955
NM_002485.5(NBN):c.2146A>G (p.Asn716Asp)	rs72563785	0.00830
NM_002485.5(NBN):c.1489A>G (p.Thr497Ala)	rs3026268	0.00711
NM_002485.5(NBN):c.*401C>G	rs104895030	0.00535
NM_002485.5(NBN):c.702+84G>C	rs104895036	0.00405
NM_002485.5(NBN):c.381T>C (p.Ala127=)	rs61754795	0.00266
NM_002485.5(NBN):c.643C>T (p.Arg215Trp)	rs34767364	0.00206
NM_002485.5(NBN):c.283G>A (p.Asp95Asn)	rs61753720	0.00188
NM_002485.5(NBN):c.511A>G (p.Ile171Val)	rs61754966	0.00145
NM_002485.5(NBN):c.172-448A>G	rs104895038	0.00115
NM_002485.5(NBN):c.481-168C>T	rs104895037	0.00096
NM_002485.5(NBN):c.628G>T (p.Val210Phe)	rs61754796	0.00047
NM_002485.5(NBN):c.1720T>A (p.Leu574Ile)	rs142334798	0.00044
NM_002485.5(NBN):c.425A>G (p.Asn142Ser)	rs769414	0.00033
NM_002485.5(NBN):c.1262T>C (p.Leu421Ser)	rs104895032	0.00027
NM_002485.5(NBN):c.1405G>T (p.Asp469Tyr)	rs148205441	0.00025
NM_002485.5(NBN):c.456G>A (p.Met152Ile)	rs201816949	0.00014
NM_002485.5(NBN):c.721G>A (p.Ala241Thr)	rs587781333	0.00004
NM_002485.5(NBN):c.702+126A>T	rs104895035	0.00003
NM_002485.5(NBN):c.2117C>G (p.Ser706Ter)	rs730881857	0.00001
NM_002485.5(NBN):c.2140C>T (p.Arg714Ter)	rs730881864	0.00001
NM_002485.5(NBN):c.520C>A (p.Pro174Thr)	rs587778546	0.00001
NM_002485.5(NBN):c.-40C>T	rs730881843
NM_002485.5(NBN):c.1089C>A (p.Tyr363Ter)	rs121908974
NM_002485.5(NBN):c.1125G>A (p.Trp375Ter)	rs1057519588
NM_002485.5(NBN):c.1142del (p.Pro381fs)	rs587781969
NM_002485.5(NBN):c.115C>A (p.Gln39Lys)	rs377730553
NM_002485.5(NBN):c.1202C>G (p.Pro401Arg)	rs104895033
NM_002485.5(NBN):c.149C>T (p.Ala50Val)	rs1554569035
NM_002485.5(NBN):c.1530G>C (p.Glu510Asp)	rs1283330641
NM_002485.5(NBN):c.1579G>T (p.Asp527Tyr)	rs104895031
NM_002485.5(NBN):c.172-529G>A	rs104895039
NM_002485.5(NBN):c.1769del (p.Arg590fs)	rs1563525004
NM_002485.5(NBN):c.1845+1G>A	rs2129695663
NM_002485.5(NBN):c.321-2A>G	rs587777931
NM_002485.5(NBN):c.330T>G (p.Tyr110Ter)	rs1057519585
NM_002485.5(NBN):c.527_538del (p.Tyr176_Glu179del)	rs1811866878
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650
NM_002485.5(NBN):c.681del (p.Phe227fs)	rs1057519586
NM_002485.5(NBN):c.698_701del (p.Lys233fs)	rs587780100
NM_002485.5(NBN):c.741_742dup (p.Glu248fs)	rs864309670
NM_002485.5(NBN):c.758C>T (p.Thr253Ile)	rs61754967
NM_002485.5(NBN):c.818C>G (p.Thr273Arg)	rs1554563912
NM_002485.5(NBN):c.836_839del (p.Gln279fs)	rs864309668
NM_002485.5(NBN):c.872A>G (p.Gln291Arg)	rs587778547
NM_002485.5(NBN):c.93_94del (p.Ala32fs)	rs864622253
NM_002485.5(NBN):c.976C>T (p.Gln326Ter)	rs121908973

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