ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 22
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NM_002485.4(NBN):c.1124+1G>C rs1057517209
NM_002485.4(NBN):c.1125-2A>G rs1554559373
NM_002485.4(NBN):c.1397+1_1397+9delinsACA rs876659666
NM_002485.4(NBN):c.163_171+3del rs1057516772
NM_002485.4(NBN):c.1846-1G>A rs61753717
NM_002485.4(NBN):c.2070+2T>G rs786203223
NM_002485.4(NBN):c.2071-1G>A rs786201965
NM_002485.4(NBN):c.2071-1G>C rs786201965
NM_002485.4(NBN):c.2184+1G>A rs756363734
NM_002485.4(NBN):c.2184+1G>T rs756363734
NM_002485.4(NBN):c.2234+2T>G rs142301194
NM_002485.4(NBN):c.320+1G>A rs1364533250
NM_002485.4(NBN):c.320+2T>G rs1563580433
NM_002485.4(NBN):c.37+1G>A rs574673404
NM_002485.4(NBN):c.37+2dup rs876658183
NM_002485.4(NBN):c.481-2A>T rs751567476
NM_002485.4(NBN):c.7A>T (p.Lys3Ter) rs779098734
NM_002485.4(NBN):c.896+1G>A rs778306619
NM_002485.4(NBN):c.896+1G>T rs778306619
NM_002485.4(NBN):c.897-2A>T rs864622090
NM_002485.4(NBN):c.994+1G>T rs1554562083
NM_002485.4(NBN):c.995-2A>G rs876659521

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