ClinVar Miner

List of variants in gene NBN reported as benign

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Gene type:
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Total variants: 58
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HGVS dbSNP
GRCh37/hg19 8q21.3(chr8:90951388-90990121)x1
NM_002485.4(NBN):c.-12G>A rs375584006
NM_002485.4(NBN):c.-26G>A rs201392451
NM_002485.4(NBN):c.-37G>A rs543890002
NM_002485.4(NBN):c.102G>A (p.Leu34=) rs1063045
NM_002485.4(NBN):c.1035C>T (p.Gly345=) rs146605798
NM_002485.4(NBN):c.1089C>T (p.Tyr363=) rs121908974
NM_002485.4(NBN):c.1124+11_1124+13del rs747584990
NM_002485.4(NBN):c.1124+18C>T rs2234744
NM_002485.4(NBN):c.1124+19C>T rs13312903
NM_002485.4(NBN):c.1124+20G>A rs201436502
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1197T>C (p.Asp399=) rs709816
NM_002485.4(NBN):c.1222A>G (p.Lys408Glu) rs34120922
NM_002485.4(NBN):c.1262T>C (p.Leu421Ser) rs104895032
NM_002485.4(NBN):c.1317A>G (p.Ile439Met) rs28538230
NM_002485.4(NBN):c.1398-18dup rs587780555
NM_002485.4(NBN):c.1398-19C>T rs201495716
NM_002485.4(NBN):c.1489A>G (p.Thr497Ala) rs3026268
NM_002485.4(NBN):c.1690G>A (p.Glu564Lys) rs72550742
NM_002485.4(NBN):c.171+133A>G
NM_002485.4(NBN):c.1720T>A (p.Leu574Ile) rs142334798
NM_002485.4(NBN):c.1809C>A (p.Phe603Leu) rs192236678
NM_002485.4(NBN):c.1882G>A (p.Glu628Lys) rs115321485
NM_002485.4(NBN):c.1914+10G>A rs577706448
NM_002485.4(NBN):c.1914+9C>T rs13312938
NM_002485.4(NBN):c.1915-7A>G rs2308962
NM_002485.4(NBN):c.2016A>G (p.Pro672=) rs1061302
NM_002485.4(NBN):c.2071-30A>T rs3736639
NM_002485.4(NBN):c.2082T>G (p.Pro694=) rs7823648
NM_002485.4(NBN):c.2146A>G (p.Asn716Asp) rs72563785
NM_002485.4(NBN):c.2196A>G (p.Gln732=) rs587780780
NM_002485.4(NBN):c.2202A>G (p.Ala734=) rs200452212
NM_002485.4(NBN):c.2220T>C (p.Ala740=) rs147494981
NM_002485.4(NBN):c.2235-172C>T
NM_002485.4(NBN):c.2235-18C>T rs138106214
NM_002485.4(NBN):c.279G>A (p.Ser93=) rs587780781
NM_002485.4(NBN):c.283G>A (p.Asp95Asn) rs61753720
NM_002485.4(NBN):c.320+200C>A
NM_002485.4(NBN):c.321-17C>G rs763878712
NM_002485.4(NBN):c.321-224T>C
NM_002485.4(NBN):c.37+10G>C rs369408590
NM_002485.4(NBN):c.37+11A>G rs115032431
NM_002485.4(NBN):c.37+5G>A rs116735828
NM_002485.4(NBN):c.38-10T>A rs556807466
NM_002485.4(NBN):c.381T>C (p.Ala127=) rs61754795
NM_002485.4(NBN):c.426T>C (p.Asn142=) rs143070291
NM_002485.4(NBN):c.441C>T (p.Cys147=) rs137857529
NM_002485.4(NBN):c.481-18A>G rs587781092
NM_002485.4(NBN):c.511A>G (p.Ile171Val) rs61754966
NM_002485.4(NBN):c.553G>C (p.Glu185Gln) rs1805794
NM_002485.4(NBN):c.643C>T (p.Arg215Trp) rs34767364
NM_002485.4(NBN):c.703-18G>A rs769418
NM_002485.4(NBN):c.797C>T (p.Pro266Leu) rs769420
NM_002485.4(NBN):c.804G>A (p.Thr268=) rs141443872
NM_002485.4(NBN):c.939G>A (p.Ala313=) rs145750430
NM_002485.4(NBN):c.995-17A>G rs372875251
NM_002485.4:c.703-20insA

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