"Ambry Genetics"[submitter] AND "SERPINF2"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2268817	NM_000934.4(SERPINF2):c.36G>C (p.Trp12Cys)	SERPINF2 (W12C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317638	NM_000934.4(SERPINF2):c.112G>A (p.Gly38Arg)	SERPINF2 (G38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226657	NM_000934.4(SERPINF2):c.116C>T (p.Pro39Leu)	SERPINF2 (P39L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610676	NM_000934.4(SERPINF2):c.170C>G (p.Pro57Arg)	SERPINF2 (P57R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616197	NM_000934.4(SERPINF2):c.196C>A (p.Pro66Thr)	SERPINF2 (P66T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618808	NM_000934.4(SERPINF2):c.224C>A (p.Thr75Asn)	SERPINF2 (T75N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477075	NM_000934.4(SERPINF2):c.248C>G (p.Ala83Gly)	SERPINF2 (A83G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394287	NM_000934.4(SERPINF2):c.251G>A (p.Arg84Gln)	SERPINF2 (R84Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2196993	NM_000934.4(SERPINF2):c.361G>A (p.Ala121Thr)	SERPINF2 (A121T)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3160489	NM_000934.4(SERPINF2):c.472G>A (p.Gly158Ser)	SERPINF2 (G158S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160491	NM_000934.4(SERPINF2):c.498G>A (p.Met166Ile)	SERPINF2 (M166I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317639	NM_000934.4(SERPINF2):c.538G>A (p.Glu180Lys)	SERPINF2 (E116K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207301	NM_000934.4(SERPINF2):c.682G>C (p.Val228Leu)	SERPINF2 (V228L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470463	NM_000934.4(SERPINF2):c.700G>A (p.Ala234Thr)	SERPINF2 (A170T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1137989	NM_000934.4(SERPINF2):c.725G>A (p.Arg242Lys)	SERPINF2 (R178K +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 808193	NM_000934.4(SERPINF2):c.852G>T (p.Glu284Asp)	SERPINF2 (E284D +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3160492	NM_000934.4(SERPINF2):c.856C>G (p.Gln286Glu)	SERPINF2 (Q286E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617195	NM_000934.4(SERPINF2):c.1083G>C (p.Gln361His)	SERPINF2 (Q297H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245747	NM_000934.4(SERPINF2):c.1096C>T (p.Arg366Cys)	SERPINF2 (R302C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568708	NM_000934.4(SERPINF2):c.1161C>G (p.Ser387Arg)	SERPINF2 (S387R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317640	NM_000934.4(SERPINF2):c.1184C>T (p.Ala395Val)	SERPINF2 (A331V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491800	NM_000934.4(SERPINF2):c.1192A>T (p.Ser398Cys)	SERPINF2 (S334C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289513	NM_000934.4(SERPINF2):c.1384G>A (p.Gly462Ser)	SERPINF2 (G462S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160488	NM_000934.4(SERPINF2):c.1393C>T (p.Arg465Cys)	SERPINF2 (R401C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309059	NM_000934.4(SERPINF2):c.1460T>C (p.Phe487Ser)	SERPINF2 (F423S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25