ClinVar Miner

List of variants in gene NEXMIF reported by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.1349del (p.Tyr450fs)	rs2147441024
NM_001008537.3(NEXMIF):c.4165A>G (p.Thr1389Ala)	rs2147438917
NM_001008537.3(NEXMIF):c.644G>A (p.Gly215Glu)	rs2147441499

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