List of variants in gene CLDN14 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_001146079.2(CLDN14):c.243C>T (p.Arg81=)	rs219779	0.25678
NM_001146079.2(CLDN14):c.687G>A (p.Thr229=)	rs219780	0.20318
NM_001146079.2(CLDN14):c.11C>T (p.Thr4Met)	rs113831133	0.04508
NM_001146079.2(CLDN14):c.63G>A (p.Thr21=)	rs117560775	0.02306
NM_001146079.2(CLDN14):c.621C>T (p.Thr207=)	rs139437157	0.00444
NM_001146079.2(CLDN14):c.*10G>C	rs139628442	0.00336
NM_001146079.2(CLDN14):c.300C>T (p.Ile100=)	rs113350364	0.00136
NM_001146079.2(CLDN14):c.406G>A (p.Val136Ile)	rs140918123	0.00112
NM_001146079.2(CLDN14):c.363C>T (p.Gly121=)	rs763411863	0.00004
NM_001146079.2(CLDN14):c.167G>A (p.Trp56Ter)	rs371100799	0.00003
NM_001146079.2(CLDN14):c.242G>A (p.Arg81His)	rs368027306	0.00001
NM_001146079.2(CLDN14):c.450G>A (p.Pro150=)	rs746102559

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