"PreventionGenetics, part of Exact Sciences"[submitter] AND "SERPINF2" - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 256836	NM_000934.4(SERPINF2):c.5C>T (p.Ala2Val)	SERPINF2 (A2V)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 256837	NM_000934.4(SERPINF2):c.97C>T (p.Arg33Trp)	SERPINF2 (R33W)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 3039899	NM_000934.4(SERPINF2):c.103-5C>T	SERPINF2	Single nucleotide variant (intron variant)	SERPINF2-related disorder	GLikely benign
Select item 256835	NM_000934.4(SERPINF2):c.186C>T (p.Ala62=)	SERPINF2	Single nucleotide variant (synonymous variant +1 more)	not specified	GBenign
Select item 724613	NM_000934.4(SERPINF2):c.412G>A (p.Ala138Thr)	SERPINF2 (A138T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3038248	NM_000934.4(SERPINF2):c.473G>A (p.Gly158Asp)	SERPINF2 (G158D +1 more)	Single nucleotide variant (missense variant)	SERPINF2-related disorder	GLikely benign
Select item 3047785	NM_000934.4(SERPINF2):c.511+6C>T	SERPINF2	Single nucleotide variant (intron variant)	SERPINF2-related disorder	GLikely benign
Select item 3028949	NM_000934.4(SERPINF2):c.699C>T (p.Asn233=)	SERPINF2	Single nucleotide variant (synonymous variant)	SERPINF2-related disorder	GLikely benign
Select item 808192	NM_000934.4(SERPINF2):c.815C>T (p.Thr272Met)	SERPINF2 (T272M +1 more)	Single nucleotide variant (missense variant)	SERPINF2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 256833	NM_000934.4(SERPINF2):c.1107C>T (p.Ser369=)	SERPINF2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3053153	NM_000934.4(SERPINF2):c.1287C>T (p.Phe429=)	SERPINF2	Single nucleotide variant (synonymous variant)	SERPINF2-related disorder	GLikely benign
Select item 256834	NM_000934.4(SERPINF2):c.1301G>A (p.Arg434Lys)	SERPINF2 (R434K +1 more)	Single nucleotide variant (missense variant)	not specified	GBenign