List of variants in gene CLPP 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006012.4(CLPP):c.497T>C (p.Met166Thr)	rs140102092	0.00001
NM_006012.4(CLPP):c.598A>G (p.Lys200Glu)	rs1057519233	0.00001
NM_006012.4(CLPP):c.343A>T (p.Ile115Phe)
NM_006012.4(CLPP):c.395T>C (p.Ile132Thr)

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