"Ambry Genetics"[submitter] AND "SERPINE2"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2370092	NM_001136528.2(SERPINE2):c.871G>T (p.Val291Leu)	SERPINE2 (V303L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160474	NM_001136528.2(SERPINE2):c.684T>G (p.Cys228Trp)	SERPINE2 (C228W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593425	NM_001136528.2(SERPINE2):c.634G>A (p.Gly212Arg)	SERPINE2 (G212R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160473	NM_001136528.2(SERPINE2):c.620T>C (p.Phe207Ser)	SERPINE2 (F219S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337430	NM_001136528.2(SERPINE2):c.547C>T (p.Leu183Phe)	SERPINE2 (L183F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407085	NM_001136528.2(SERPINE2):c.421G>A (p.Val141Met)	SERPINE2 (V141M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320336	NM_001136528.2(SERPINE2):c.383C>G (p.Thr128Arg)	SERPINE2 (T128R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395919	NM_001136528.2(SERPINE2):c.340G>A (p.Val114Met)	SERPINE2 (V126M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546521	NM_001136528.2(SERPINE2):c.305A>G (p.Lys102Arg)	SERPINE2 (K114R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160472	NM_001136528.2(SERPINE2):c.298G>A (p.Val100Ile)	SERPINE2 (V100I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160471	NM_001136528.2(SERPINE2):c.290A>G (p.Lys97Arg)	SERPINE2 (K109R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557201	NM_001136528.2(SERPINE2):c.253G>A (p.Val85Ile)	SERPINE2 (V97I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510627	NM_001136528.2(SERPINE2):c.157A>G (p.Ile53Val)	SERPINE2 (I53V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2476729	NM_001136528.2(SERPINE2):c.107T>C (p.Ile36Thr)	SERPINE2 (I48T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526299	NM_001136528.2(SERPINE2):c.101C>T (p.Thr34Met)	SERPINE2 (T34M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160475	NM_001136528.2(SERPINE2):c.46C>T (p.Pro16Ser)	SERPINE2 (P16S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance