List of variants in gene CPA1 reported by PreventionGenetics, part of Exact Sciences

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001868.4(CPA1):c.474C>T (p.Tyr158=)	rs968404	0.13541
NM_001868.4(CPA1):c.321C>T (p.Phe107=)	rs116214014	0.00316
NM_001868.4(CPA1):c.816G>A (p.Ser272=)	rs34843162	0.00217
NM_001868.4(CPA1):c.497G>A (p.Gly166Asp)	rs144546424	0.00209
NM_001868.4(CPA1):c.621C>T (p.Thr207=)	rs61735158	0.00205
NM_001868.4(CPA1):c.371C>T (p.Thr124Ile)	rs150653308	0.00165
NM_001868.4(CPA1):c.5G>A (p.Arg2Gln)	rs145988366	0.00030
NM_001868.4(CPA1):c.492G>A (p.Thr164=)	rs369058363	0.00016
NM_001868.4(CPA1):c.825C>T (p.Tyr275=)	rs782346209	0.00002
NM_001868.4(CPA1):c.165G>C (p.Gly55=)	rs1126899
NM_001868.4(CPA1):c.600C>T (p.Tyr200=)	rs12706927
NM_001868.4(CPA1):c.788-5C>G	rs201705049

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