ClinVar Miner

List of variants in gene NEFL reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_006158.5(NEFL):c.*1256G>A rs2979704 0.77789
NM_006158.5(NEFL):c.*687G>C rs2976439 0.53745
NM_006158.4(NEFL):c.-176C>A rs2979688 0.53692
NM_006158.5(NEFL):c.*426G>A rs73546943 0.06709
NM_006158.5(NEFL):c.1407G>A (p.Glu469=) rs543609297 0.00777
NM_006158.5(NEFL):c.*1344G>A rs79034217 0.00743
NM_006158.5(NEFL):c.*101A>G rs34505194 0.00356
NM_006158.5(NEFL):c.*244A>G rs78869168 0.00290
NM_006158.5(NEFL):c.*82T>A rs148654058 0.00222
NM_006158.5(NEFL):c.1402G>A (p.Asp468Asn) rs57153321 0.00081
NM_006158.5(NEFL):c.639C>G (p.Ile213Met) rs62636522 0.00065
NM_006158.5(NEFL):c.*1293A>G rs573350915 0.00043
NM_006158.5(NEFL):c.*878A>G rs189452316 0.00034
NM_006158.5(NEFL):c.*1806T>C rs192937928 0.00021
NM_006158.5(NEFL):c.227T>C (p.Val76Ala) rs58907919 0.00013
NM_006158.4(NEFL):c.-183C>G rs62503766
NM_006158.5(NEFL):c.*235A>T rs1059111
NM_006158.5(NEFL):c.*486T>G rs562682645

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