ClinVar Miner

List of variants in gene NEXMIF reported by Mendelics

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.1882C>T (p.Arg628Ter)	rs786205208
NM_001008537.3(NEXMIF):c.2869C>T (p.Gln957Ter)	rs2147439880
NM_001008537.3(NEXMIF):c.3689del (p.Ala1230fs)	rs1602210960

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