ClinVar Miner

List of variants in gene NBN reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
LRG_158t1:c.703-20insA
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.1089C>T (p.Tyr363=) rs121908974
NM_002485.4(NBN):c.1124+11_1124+13delTTC rs747584990
NM_002485.4(NBN):c.1124+20G>A rs201436502
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1398-10dupT 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.1882G>A (p.Glu628Lys) rs115321485
NM_002485.4(NBN):c.1914+10G>A rs577706448
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.2235-18C>T rs138106214
NM_002485.4(NBN):c.279G>A (p.Ser93=) rs587780781
NM_002485.4(NBN):c.321-17C>G rs763878712
NM_002485.4(NBN):c.37+10G>C rs369408590
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.481-18A>G rs587781092
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

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