ClinVar Miner

List of variants in gene NBN reported by Integrated Genetics/Laboratory Corporation of America

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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP
NM_002485.4(NBN):c.-10A>T rs759094270
NM_002485.4(NBN):c.1009A>G (p.Thr337Ala) rs1554560492
NM_002485.4(NBN):c.1035C>T (p.Gly345=) rs146605798
NM_002485.4(NBN):c.1036G>A (p.Val346Met) rs200297914
NM_002485.4(NBN):c.1056A>G (p.Leu352=) rs369092711
NM_002485.4(NBN):c.1065C>T (p.Ser355=) rs876659205
NM_002485.4(NBN):c.1066G>A (p.Ala356Thr) rs777259845
NM_002485.4(NBN):c.1089C>T (p.Tyr363=) rs121908974
NM_002485.4(NBN):c.1099A>G (p.Thr367Ala) rs1554560363
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1194A>G (p.Gln398=) rs200046373
NM_002485.4(NBN):c.119C>T (p.Ser40Leu) rs587781530
NM_002485.4(NBN):c.1222A>G (p.Lys408Glu) rs34120922
NM_002485.4(NBN):c.1238A>G (p.Asn413Ser) rs529340553
NM_002485.4(NBN):c.1247T>C (p.Met416Thr) rs863224713
NM_002485.4(NBN):c.1262T>C (p.Leu421Ser) rs104895032
NM_002485.4(NBN):c.1282A>G (p.Asn428Asp) rs786202302
NM_002485.4(NBN):c.1313G>T (p.Ser438Ile) rs786203131
NM_002485.4(NBN):c.1317A>G (p.Ile439Met) rs28538230
NM_002485.4(NBN):c.1354A>C (p.Thr452Pro) rs141137543
NM_002485.4(NBN):c.1370A>G (p.Asn457Ser) rs876659312
NM_002485.4(NBN):c.1405G>T (p.Asp469Tyr) rs148205441
NM_002485.4(NBN):c.1484C>T (p.Pro495Leu) rs863224714
NM_002485.4(NBN):c.1515del (p.Glu505fs) rs759232053
NM_002485.4(NBN):c.1520_1523ATCT[1] (p.Ser509fs) rs1554558449
NM_002485.4(NBN):c.156_157del (p.Ser53fs) rs767454740
NM_002485.4(NBN):c.1603T>G (p.Ser535Ala) rs1563526265
NM_002485.4(NBN):c.1628A>G (p.Glu543Gly) rs587781624
NM_002485.4(NBN):c.1666G>A (p.Val556Met) rs771567358
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.1729G>T (p.Asp577Tyr) rs587781881
NM_002485.4(NBN):c.175C>T (p.Gln59Ter) rs1554568427
NM_002485.4(NBN):c.1769G>C (p.Arg590Thr) rs1563524967
NM_002485.4(NBN):c.1809C>A (p.Phe603Leu) rs192236678
NM_002485.4(NBN):c.1816G>A (p.Glu606Lys) rs774324419
NM_002485.4(NBN):c.1882G>A (p.Glu628Lys) rs115321485
NM_002485.4(NBN):c.1925A>G (p.Lys642Arg) rs587781547
NM_002485.4(NBN):c.1930C>A (p.Gln644Lys) rs764050423
NM_002485.4(NBN):c.1995A>G (p.Lys665=) rs1554556540
NM_002485.4(NBN):c.2071-1G>A rs786201965
NM_002485.4(NBN):c.207A>G (p.Lys69=) rs754352569
NM_002485.4(NBN):c.2117C>G (p.Ser706Ter) rs730881857
NM_002485.4(NBN):c.2136T>C (p.His712=) rs1429343146
NM_002485.4(NBN):c.2140C>T (p.Arg714Ter) rs730881864
NM_002485.4(NBN):c.2146A>G (p.Asn716Asp) rs72563785
NM_002485.4(NBN):c.2149A>T (p.Thr717Ser) rs587780093
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.2215C>G (p.Leu739Val) rs370058152
NM_002485.4(NBN):c.278C>T (p.Ser93Leu) rs12721593
NM_002485.4(NBN):c.280G>A (p.Gly94Arg) rs1563580785
NM_002485.4(NBN):c.283G>A (p.Asp95Asn) rs61753720
NM_002485.4(NBN):c.333G>A (p.Glu111=) rs376455714
NM_002485.4(NBN):c.37+6G>C rs540868733
NM_002485.4(NBN):c.384A>G (p.Leu128=) rs587780782
NM_002485.4(NBN):c.425A>G (p.Asn142Ser) rs769414
NM_002485.4(NBN):c.441C>T (p.Cys147=) rs137857529
NM_002485.4(NBN):c.456G>A (p.Met152Ile) rs201816949
NM_002485.4(NBN):c.468A>C (p.Lys156Asn) rs730881858
NM_002485.4(NBN):c.481-2A>T rs751567476
NM_002485.4(NBN):c.483A>G (p.Thr161=) rs758276775
NM_002485.4(NBN):c.505C>T (p.Arg169Cys) rs182756889
NM_002485.4(NBN):c.506G>A (p.Arg169His) rs776134250
NM_002485.4(NBN):c.511A>G (p.Ile171Val) rs61754966
NM_002485.4(NBN):c.517A>G (p.Lys173Glu) rs1563574056
NM_002485.4(NBN):c.547G>A (p.Ala183Thr) rs151070415
NM_002485.4(NBN):c.621T>C (p.Ser207=) rs876658177
NM_002485.4(NBN):c.628G>T (p.Val210Phe) rs61754796
NM_002485.4(NBN):c.643C>T (p.Arg215Trp) rs34767364
NM_002485.4(NBN):c.644G>A (p.Arg215Gln) rs61753718
NM_002485.4(NBN):c.657_661del (p.Lys219fs) rs587776650
NM_002485.4(NBN):c.683T>G (p.Ile228Arg) rs777460725
NM_002485.4(NBN):c.698_701del (p.Lys233fs) rs587780100
NM_002485.4(NBN):c.702+8T>C rs1563561325
NM_002485.4(NBN):c.758C>T (p.Thr253Ile) rs61754967
NM_002485.4(NBN):c.775G>A (p.Glu259Lys) rs201559159
NM_002485.4(NBN):c.804G>A (p.Thr268=) rs141443872
NM_002485.4(NBN):c.832T>G (p.Ser278Ala) rs1225178489
NM_002485.4(NBN):c.897-2A>T rs864622090
NM_002485.4(NBN):c.925G>A (p.Glu309Lys) rs587780101
NM_002485.4(NBN):c.930T>A (p.Ile310=) rs142813526
NM_002485.4(NBN):c.939G>A (p.Ala313=) rs145750430
NM_002485.4(NBN):c.940G>A (p.Val314Met) rs529845940

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