List of variants in gene NEXMIF reported by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.4246C>T (p.Pro1416Ser)	rs143577015	0.00258
NM_001008537.3(NEXMIF):c.2098G>C (p.Val700Leu)	rs141776597	0.00038
NM_001008537.3(NEXMIF):c.3823A>G (p.Ser1275Gly)	rs201434271	0.00012
NM_001008537.3(NEXMIF):c.4422G>A (p.Lys1474=)	rs371190782	0.00009
NM_001008537.3(NEXMIF):c.3222G>A (p.Pro1074=)	rs748567167	0.00001
NM_001008537.3(NEXMIF):c.4363A>C (p.Lys1455Gln)	rs2147438722

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