List of variants in gene TECPR2 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014844.5(TECPR2):c.2330G>A (p.Ser777Asn)	rs144849839	0.00038
NM_014844.5(TECPR2):c.3797G>T (p.Gly1266Val)	rs201704673	0.00012
NM_014844.5(TECPR2):c.1125C>T (p.Val375=)	rs144187959	0.00011
NM_014844.5(TECPR2):c.818G>A (p.Arg273His)	rs144069125	0.00011
NM_014844.5(TECPR2):c.815C>T (p.Pro272Leu)	rs756747141	0.00001
NM_014844.5(TECPR2):c.1249G>A (p.Asp417Asn)
NM_014844.5(TECPR2):c.1417+3A>G	rs2139727319
NM_014844.5(TECPR2):c.1606G>A (p.Gly536Ser)	rs186595127
NM_014844.5(TECPR2):c.1687G>A (p.Glu563Lys)
NM_014844.5(TECPR2):c.2092T>G (p.Trp698Gly)
NM_014844.5(TECPR2):c.3148G>A (p.Val1050Met)	rs2139751290
NM_014844.5(TECPR2):c.4017C>T (p.Val1339=)
NM_014844.5(TECPR2):c.4135C>T (p.Arg1379Trp)

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