ClinVar Miner

List of variants in gene NOTCH2 reported as likely benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 14
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NM_024408.4(NOTCH2):c.1443G>A (p.Leu481=) rs587674318
NM_024408.4(NOTCH2):c.1541A>G (p.Asn514Ser) rs34308573
NM_024408.4(NOTCH2):c.1681+9C>A rs192886452
NM_024408.4(NOTCH2):c.3441G>A (p.Glu1147=) rs371875533
NM_024408.4(NOTCH2):c.4122C>T (p.Cys1374=) rs74117504
NM_024408.4(NOTCH2):c.4897G>A (p.Val1633Ile) rs116321057
NM_024408.4(NOTCH2):c.4999G>A (p.Val1667Ile) rs17024517
NM_024408.4(NOTCH2):c.4999G>T (p.Val1667Phe) rs17024517
NM_024408.4(NOTCH2):c.6223G>A (p.Val2075Met) rs150516342
NM_024408.4(NOTCH2):c.6486C>T (p.Ser2162=) rs372865598
NM_024408.4(NOTCH2):c.6516C>T (p.Ser2172=) rs587733506
NM_024408.4(NOTCH2):c.6997G>C (p.Ala2333Pro) rs143506822
NM_024408.4(NOTCH2):c.7086C>T (p.Asp2362=) rs150657714
NM_024408.4(NOTCH2):c.7223T>A (p.Leu2408His) rs35586704

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