List of variants reported as uncertain significance for benign neoplasm by Revvity Omics, Revvity

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005401.5(PTPN14):c.*6320C>T
NM_005401.5(PTPN14):c.-154-22749A>G
NM_005401.5(PTPN14):c.-154-42562G>A
NM_005401.5(PTPN14):c.679G>T (p.Gly227Ter)

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