List of variants in gene PTPN14 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005401.5(PTPN14):c.1079A>C (p.His360Pro)	rs112523432	0.00547
NM_005401.5(PTPN14):c.1253G>A (p.Ser418Asn)	rs141247660	0.00447
NM_005401.5(PTPN14):c.1200G>A (p.Ser400=)	rs12404313	0.00373
NM_005401.5(PTPN14):c.2002C>T (p.Arg668Cys)	rs61749334	0.00237
NM_005401.5(PTPN14):c.1059C>T (p.Thr353=)	rs116652390	0.00203
NM_005401.5(PTPN14):c.581+5G>A	rs143408016	0.00132
NM_005401.5(PTPN14):c.3137C>G (p.Thr1046Arg)

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