List of variants in gene CPOX 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_000097.7(CPOX):c.520G>A (p.Ala174Thr)	rs199514514	0.00016
NM_000097.7(CPOX):c.1138C>G (p.Gln380Glu)	rs201231166	0.00003
NM_000097.7(CPOX):c.1253T>C (p.Leu418Ser)	rs2107113916
NM_000097.7(CPOX):c.1277+8G>A
NM_000097.7(CPOX):c.995G>A (p.Arg332Gln)	rs781627991

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