ClinVar Miner

List of variants in gene NBN reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_002485.4(NBN):c.1035C>T (p.Gly345=) rs146605798
NM_002485.4(NBN):c.1056A>G (p.Leu352=) rs369092711
NM_002485.4(NBN):c.1107A>G (p.Ser369=)
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1222A>G (p.Lys408Glu) rs34120922
NM_002485.4(NBN):c.1232C>G (p.Ser411Cys) rs551032019
NM_002485.4(NBN):c.1317A>G (p.Ile439Met) rs28538230
NM_002485.4(NBN):c.1338T>C (p.Ala446=) rs1373132755
NM_002485.4(NBN):c.1419A>G (p.Gln473=) rs587780535
NM_002485.4(NBN):c.1690G>A (p.Glu564Lys) rs72550742
NM_002485.4(NBN):c.171+4T>C rs587782290
NM_002485.4(NBN):c.1720T>A (p.Leu574Ile) rs142334798
NM_002485.4(NBN):c.1882G>A (p.Glu628Lys) rs115321485
NM_002485.4(NBN):c.1890A>C (p.Ser630=) rs587780778
NM_002485.4(NBN):c.1914+10G>A rs577706448
NM_002485.4(NBN):c.1915-11C>T
NM_002485.4(NBN):c.1915-6T>C
NM_002485.4(NBN):c.2139T>C (p.Ala713=) rs755274971
NM_002485.4(NBN):c.2185-122T>C
NM_002485.4(NBN):c.2196A>G (p.Gln732=) rs587780780
NM_002485.4(NBN):c.2234+157A>G
NM_002485.4(NBN):c.2234+16C>T rs1563497498
NM_002485.4(NBN):c.2235-18C>T rs138106214
NM_002485.4(NBN):c.283G>A (p.Asp95Asn) rs61753720
NM_002485.4(NBN):c.37+5G>A rs116735828
NM_002485.4(NBN):c.38-10T>A rs556807466
NM_002485.4(NBN):c.38-19A>T rs766849651
NM_002485.4(NBN):c.381T>C (p.Ala127=) rs61754795
NM_002485.4(NBN):c.453C>T (p.Val151=) rs1176879721
NM_002485.4(NBN):c.643C>T (p.Arg215Trp) rs34767364
NM_002485.4(NBN):c.702+9G>A rs748373099
NM_002485.4(NBN):c.703-14C>T rs1411178267
NM_002485.4(NBN):c.897-42G>C
NM_002485.4(NBN):c.939G>A (p.Ala313=) rs145750430
NM_002485.4:c.1124+37C>G
NM_002485.4:c.172-3C>T
NM_002485.4:c.2070+4G>A

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