ClinVar Miner

List of variants in gene NBN reported as pathogenic for Hereditary cancer-predisposing syndrome

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Gene type:
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Total variants: 74
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HGVS dbSNP
NM_002485.4(NBN):c.1029dup (p.Gln344Thrfs)
NM_002485.4(NBN):c.1030C>T rs767215758
NM_002485.4(NBN):c.1040C>G (p.Ser347Ter) rs876660290
NM_002485.4(NBN):c.1089C>A (p.Tyr363Ter) rs121908974
NM_002485.4(NBN):c.1124G>A (p.Trp375Ter) rs1394437421
NM_002485.4(NBN):c.1142delC (p.Pro381Glnfs) rs587781969
NM_002485.4(NBN):c.1150delA (p.Ile384Serfs) rs1554559348
NM_002485.4(NBN):c.115delC (p.Gln39Serfs) rs864622511
NM_002485.4(NBN):c.1171C>T (p.Gln391Ter) rs1554559323
NM_002485.4(NBN):c.1186delC (p.Leu396Phefs) rs1554559314
NM_002485.4(NBN):c.11delT (p.Leu4Argfs) rs1064793210
NM_002485.4(NBN):c.123delC (p.Ser42Alafs) rs587781891
NM_002485.4(NBN):c.127C>T (p.Arg43Ter) rs200287925
NM_002485.4(NBN):c.1336delG (p.Ala446Leufs) rs1554559083
NM_002485.4(NBN):c.1366delA (p.Arg456Glufs) rs1554559038
NM_002485.4(NBN):c.1396dup (p.Arg466Lysfs) rs1349928568
NM_002485.4(NBN):c.1397+1delG rs1060503467
NM_002485.4(NBN):c.1399G>T (p.Glu467Ter) rs1554558613
NM_002485.4(NBN):c.1419_1431dupAGAAATGTCTTCA (p.Cys478Argfs) rs864622333
NM_002485.4(NBN):c.141_142delGT (p.Leu48Asnfs) rs750375741
NM_002485.4(NBN):c.1474C>T (p.Gln492Ter) rs587782130
NM_002485.4(NBN):c.1483_1484delCCinsA (p.Pro495Metfs) rs764884516
NM_002485.4(NBN):c.1502G>A (p.Trp501Ter) rs1554558472
NM_002485.4(NBN):c.1515delG (p.Glu505Aspfs) rs759232053
NM_002485.4(NBN):c.1550_1551insA (p.Asn517Lysfs) rs587782344
NM_002485.4(NBN):c.1554dup (p.Asp519Argfs) rs1554558423
NM_002485.4(NBN):c.156_157delTT (p.Ser53Cysfs) rs767454740
NM_002485.4(NBN):c.1583delT (p.Leu528Terfs) rs1554558406
NM_002485.4(NBN):c.1612_1696del85 (p.Lys538Tyrfs) rs1554558319
NM_002485.4(NBN):c.1648_1651delAAAA (p.Lys550Glyfs) rs766044684
NM_002485.4(NBN):c.1651dupA (p.Arg551Lysfs) rs766044684
NM_002485.4(NBN):c.1716dupA (p.Glu573Argfs) rs1060503483
NM_002485.4(NBN):c.1723G>T (p.Glu575Ter) rs786201745
NM_002485.4(NBN):c.1747C>T (p.Gln583Ter) rs864622143
NM_002485.4(NBN):c.181_182delGA (p.Asp61Terfs) rs768378152
NM_002485.4(NBN):c.183delT (p.Asp61Glufs) rs587782147
NM_002485.4(NBN):c.1882_1885delGAAG (p.Glu628Thrfs) rs1178384498
NM_002485.4(NBN):c.188delT (p.Ile63Thrfs) rs876659592
NM_002485.4(NBN):c.1903A>T (p.Lys635Ter) rs587782545
NM_002485.4(NBN):c.1940delG (p.Ser647Metfs) rs1554556587
NM_002485.4(NBN):c.1974delA (p.Glu658Aspfs) rs1057516668
NM_002485.4(NBN):c.1986_1999del14 (p.Val663Tyrfs) rs587782653
NM_002485.4(NBN):c.2041C>T (p.Gln681Ter) rs1554556485
NM_002485.4(NBN):c.2056A>T (p.Lys686Ter) rs786203920
NM_002485.4(NBN):c.210_211delTA (p.Asp70Glufs) rs786202494
NM_002485.4(NBN):c.2117C>G (p.Ser706Ter) rs730881857
NM_002485.4(NBN):c.2140C>T (p.Arg714Ter) rs730881864
NM_002485.4(NBN):c.2161G>T (p.Glu721Ter) rs1064795816
NM_002485.4(NBN):c.266_270dup (p.Leu91Glufs)
NM_002485.4(NBN):c.306delT (p.Phe102Leufs) rs587781305
NM_002485.4(NBN):c.328delT (p.Tyr110Metfs) rs1554568029
NM_002485.4(NBN):c.445delC (p.His149Thrfs) rs1554567892
NM_002485.4(NBN):c.535_537delGAAinsT (p.Glu179Phefs) rs1554566678
NM_002485.4(NBN):c.55_56delTT (p.Leu19Aspfs) rs876659305
NM_002485.4(NBN):c.565C>T (p.Gln189Ter) rs1198614767
NM_002485.4(NBN):c.574C>T (p.Gln192Ter) rs1554566613
NM_002485.4(NBN):c.585-1_585delGTinsC rs786203662
NM_002485.4(NBN):c.591_603delCCCACCTCTTGATinsTTG (p.Pro198Trpfs) rs1554564297
NM_002485.4(NBN):c.657_661delACAAA (p.Lys219Asnfs) rs587776650
NM_002485.4(NBN):c.698_701delAACA (p.Lys233Serfs) rs587780100
NM_002485.4(NBN):c.75dup (p.Val26Cysfs) rs1199711768
NM_002485.4(NBN):c.800dup (p.Thr268Asnfs) rs1554563955
NM_002485.4(NBN):c.808_809delGT (p.Val270Cysfs) rs786202490
NM_002485.4(NBN):c.817dupA (p.Thr273Asnfs) rs730881839
NM_002485.4(NBN):c.83_89delGGAAAAA (p.Arg28Thrfs) rs1554569106
NM_002485.4(NBN):c.842T>G rs786205135
NM_002485.4(NBN):c.844dup (p.Ile282Asnfs) rs1554563861
NM_002485.4(NBN):c.88_89delAA (p.Asn30Leufs) rs587781718
NM_002485.4(NBN):c.917delC (p.Pro306Leufs) rs1554562185
NM_002485.4(NBN):c.93_94delTG (p.Ala32Hisfs) rs864622253
NM_002485.4(NBN):c.976C>T (p.Gln326Ter) rs121908973
NM_002485.4:c.1155dup
NM_002485.4:c.448delC
NM_002485.4:c.844del

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