List of variants in gene CP reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000096.4(CP):c.938C>T (p.Thr313Ile)	rs144401501	0.00037
NM_000096.4(CP):c.1217C>A (p.Ala406Glu)	rs147034302	0.00019
NM_000096.4(CP):c.181G>T (p.Asp61Tyr)	rs1576783306	0.00001
NM_000096.4(CP):c.1100G>A (p.Arg367His)
NM_000096.4(CP):c.1174A>T (p.Ile392Phe)
NM_000096.4(CP):c.2407_2409delinsCAT (p.Glu803His)
NM_000096.4(CP):c.2741T>G (p.Leu914Arg)	rs147434775
NM_000096.4(CP):c.2989C>T (p.His997Tyr)

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