List of variants in gene NEXMIF reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.2332_2333delinsTG (p.Glu778Trp)	rs1556016488
NM_001008537.3(NEXMIF):c.3041G>C (p.Cys1014Ser)
NM_001008537.3(NEXMIF):c.3321C>G (p.Asp1107Glu)
NM_001008537.3(NEXMIF):c.620T>A (p.Phe207Tyr)	rs2147441516
NM_001008537.3(NEXMIF):c.938G>A (p.Arg313Gln)	rs1247214773

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