List of variants in gene CLDN14 reported as likely benign 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001146079.2(CLDN14):c.*10G>C	rs139628442	0.00336
NM_001146079.2(CLDN14):c.690C>T (p.His230=)	rs149733854	0.00050
NM_001146079.2(CLDN14):c.102G>A (p.Ala34=)	rs146395322	0.00045
NM_001146079.2(CLDN14):c.294C>T (p.Ala98=)	rs374400022	0.00010
NM_001146079.2(CLDN14):c.591G>A (p.Pro197=)	rs374840285	0.00010
NM_001146079.2(CLDN14):c.525C>T (p.Leu175=)	rs373226526	0.00002
NM_001146079.2(CLDN14):c.105C>T (p.His35=)	rs560763542	0.00001
NM_001146079.2(CLDN14):c.681G>A (p.Ser227=)	rs763085148	0.00001
NM_001146079.2(CLDN14):c.91C>A (p.Arg31=)

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