ClinVar Miner

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

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Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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NM_024408.4(NOTCH2):c.1315G>A (p.Ala439Thr) rs199565938
NM_024408.4(NOTCH2):c.2026+6G>T rs587731563
NM_024408.4(NOTCH2):c.2042T>A (p.Ile681Asn) rs74882029
NM_024408.4(NOTCH2):c.2585C>T (p.Ala862Val) rs35656321
NM_024408.4(NOTCH2):c.3519C>T (p.Cys1173=) rs115325955
NM_024408.4(NOTCH2):c.3625T>G (p.Phe1209Val) rs147223770
NM_024408.4(NOTCH2):c.3980A>G (p.Asp1327Gly) rs61752484
NM_024408.4(NOTCH2):c.4238T>A (p.Leu1413His) rs41313282
NM_024408.4(NOTCH2):c.4305G>A (p.Arg1435=) rs6692009
NM_024408.4(NOTCH2):c.4311C>T (p.Gly1437=) rs34561092
NM_024408.4(NOTCH2):c.6094C>A (p.His2032Asn) rs143236410
NM_024408.4(NOTCH2):c.6479A>G (p.Tyr2160Cys) rs35216058
NM_024408.4(NOTCH2):c.6924G>A (p.Gln2308=)
NM_024408.4(NOTCH2):c.7042T>C (p.Leu2348=) rs61734328
NM_024408.4(NOTCH2):c.7075C>G (p.Pro2359Ala) rs75831573
NM_024408.4(NOTCH2):c.7341T>A (p.Gly2447=) rs6685892

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