ClinVar Miner

List of variants in gene NBN reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_002485.4(NBN):c.-2C>A rs202104448
NM_002485.4(NBN):c.1036G>A (p.Val346Met) rs200297914
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.1247T>C (p.Met416Thr) rs863224713
NM_002485.4(NBN):c.1262T>C (p.Leu421Ser) rs104895032
NM_002485.4(NBN):c.1313G>T (p.Ser438Ile) rs786203131
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.1373A>G (p.Tyr458Cys) rs544909538
NM_002485.4(NBN):c.1430C>T (p.Ser477Leu) rs767123014
NM_002485.4(NBN):c.1484C>T (p.Pro495Leu) rs863224714
NM_002485.4(NBN):c.153_155delinsGTG (p.Asn51_Phe52delinsLysCys) rs1064794651
NM_002485.4(NBN):c.1588T>C (p.Ser530Pro) rs1554558401
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.1720T>A (p.Leu574Ile) rs142334798
NM_002485.4(NBN):c.1729G>T (p.Asp577Tyr) rs587781881
NM_002485.4(NBN):c.1769G>C (p.Arg590Thr) rs1563524967
NM_002485.4(NBN):c.1777C>G (p.Pro593Ala) rs146989944
NM_002485.4(NBN):c.1842A>G (p.Ile614Met) rs770345026
NM_002485.4(NBN):c.1888T>C (p.Ser630Pro) rs377132067
NM_002485.4(NBN):c.1914+10G>A rs577706448
NM_002485.4(NBN):c.1925A>G (p.Lys642Arg) rs587781547
NM_002485.4(NBN):c.2038G>A (p.Gly680Ser) rs200564603
NM_002485.4(NBN):c.2071-4A>G rs746994234
NM_002485.4(NBN):c.207A>G (p.Lys69=) rs754352569
NM_002485.4(NBN):c.2136T>C (p.His712=) rs1429343146
NM_002485.4(NBN):c.2149A>T (p.Thr717Ser) rs587780093
NM_002485.4(NBN):c.2234+9T>G rs1446505128
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.340G>T (p.Val114Phe) rs771034958
NM_002485.4(NBN):c.425A>G (p.Asn142Ser) rs769414
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.483A>G (p.Thr161=) rs758276775
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.572C>T (p.Pro191Leu) rs876661071
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.702+8T>C rs1563561325
NM_002485.4(NBN):c.702+9G>A rs748373099
NM_002485.4(NBN):c.73G>A (p.Val25Ile) rs587781748
NM_002485.4(NBN):c.775G>A (p.Glu259Lys) rs201559159
NM_002485.4(NBN):c.788T>C (p.Phe263Ser) rs147626427
NM_002485.4(NBN):c.803C>T (p.Thr268Met) rs535602436
NM_002485.4(NBN):c.804G>A (p.Thr268=) rs141443872
NM_002485.4(NBN):c.940G>A (p.Val314Met) rs529845940
NM_002485.4(NBN):c.968G>A (p.Cys323Tyr) rs730881848

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