ClinVar Miner

List of variants in gene NBN reported as likely benign by PreventionGenetics

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Gene type:
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Total variants: 16
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HGVS dbSNP
NM_002485.4(NBN):c.1089C>T (p.Tyr363=) rs121908974
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1419A>G (p.Gln473=) rs587780535
NM_002485.4(NBN):c.171+4T>C rs587782290
NM_002485.4(NBN):c.1720T>A (p.Leu574Ile) rs142334798
NM_002485.4(NBN):c.1890A>C (p.Ser630=) rs587780778
NM_002485.4(NBN):c.1914+10G>A rs577706448
NM_002485.4(NBN):c.1915-11C>T
NM_002485.4(NBN):c.2234+16C>T rs1563497498
NM_002485.4(NBN):c.2235-18C>T rs138106214
NM_002485.4(NBN):c.283G>A (p.Asp95Asn) rs61753720
NM_002485.4(NBN):c.38-19A>T rs766849651
NM_002485.4(NBN):c.453C>T (p.Val151=) rs1176879721
NM_002485.4(NBN):c.702+9G>A rs748373099
NM_002485.4(NBN):c.703-14C>T rs1411178267
NM_002485.4(NBN):c.939G>A (p.Ala313=) rs145750430

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