ClinVar Miner

List of variants in gene DLL4 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_019074.4(DLL4):c.658+160G>A rs3212278 0.57271
NM_019074.4(DLL4):c.336+173G>C rs12441495 0.08234
NM_019074.4(DLL4):c.1021-46C>T rs2277538 0.07122
NM_019074.4(DLL4):c.659-77C>T rs7174607 0.03386
NM_019074.4(DLL4):c.67-20C>T rs3212277 0.02146
NM_019074.4(DLL4):c.1074T>C (p.His358=) rs28568593 0.01647
NM_019074.4(DLL4):c.1239C>T (p.Asn413=) rs35748882 0.01422
NM_019074.4(DLL4):c.369C>T (p.His123=) rs187700175 0.00244
NM_019074.4(DLL4):c.516G>C (p.Arg172=) rs202138470 0.00125
NM_019074.4(DLL4):c.672G>A (p.Ser224=) rs61757617 0.00125
NM_019074.4(DLL4):c.336+17C>T rs369890870 0.00118
NM_019074.4(DLL4):c.762C>T (p.Ile254=) rs76686366 0.00089
NM_019074.4(DLL4):c.337-20C>T rs200269380 0.00082
NM_019074.4(DLL4):c.395-18G>C rs377573739 0.00050
NM_019074.4(DLL4):c.1561G>A (p.Val521Met) rs189323864 0.00036
NM_019074.4(DLL4):c.897G>A (p.Thr299=) rs374507826 0.00033
NM_019074.4(DLL4):c.39A>T (p.Leu13=) rs202204117 0.00021
NM_019074.4(DLL4):c.720-10T>C rs200244751 0.00017
NM_019074.4(DLL4):c.1431G>A (p.Val477=) rs540754224
NM_019074.4(DLL4):c.1497C>T (p.Leu499=)
NM_019074.4(DLL4):c.1572G>A (p.Pro524=)
NM_019074.4(DLL4):c.1864C>G (p.Leu622Val)
NM_019074.4(DLL4):c.659-89G>T rs3212279
NM_019074.4(DLL4):c.851-209dup rs561583510
NM_019074.4(DLL4):c.851-307G>A rs111258544

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