"Ambry Genetics"[submitter] AND "SERPINB8"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2483657	NM_002640.4(SERPINB8):c.35C>G (p.Ala12Gly)	SERPINB8 (A12G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160445	NM_002640.4(SERPINB8):c.130A>G (p.Met44Val)	SERPINB8 (M44V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365538	NM_002640.4(SERPINB8):c.197T>C (p.Ile66Thr)	SERPINB8 (I66T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2239783	NM_002640.4(SERPINB8):c.288G>C (p.Lys96Asn)	SERPINB8 (K96N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2551361	NM_002640.4(SERPINB8):c.362T>G (p.Phe121Cys)	SERPINB8 (F121C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2230302	NM_002640.4(SERPINB8):c.535T>C (p.Tyr179His)	SERPINB8 (Y179H)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 3160446	NM_002640.4(SERPINB8):c.547A>G (p.Met183Val)	SERPINB8 (M183V +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2622428	NM_002640.4(SERPINB8):c.613A>G (p.Met205Val)	SERPINB8 (M25V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494412	NM_002640.4(SERPINB8):c.625G>C (p.Asp209His)	SERPINB8 (D27H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2075683	NM_002640.4(SERPINB8):c.658T>C (p.Tyr220His)	SERPINB8 (Y220H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2343092	NM_002640.4(SERPINB8):c.659A>G (p.Tyr220Cys)	SERPINB8 (Y220C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321817	NM_002640.4(SERPINB8):c.685A>T (p.Ile229Phe)	SERPINB8 (I47F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261027	NM_002640.4(SERPINB8):c.695C>G (p.Pro232Arg)	SERPINB8 (P50R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269515	NM_002640.4(SERPINB8):c.766T>G (p.Ser256Ala)	SERPINB8 (S256A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160448	NM_002640.4(SERPINB8):c.790G>T (p.Val264Phe)	SERPINB8 (V84F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454888	NM_002640.4(SERPINB8):c.796G>A (p.Val266Ile)	SERPINB8 (V266I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160449	NM_002640.4(SERPINB8):c.809G>C (p.Arg270Thr)	SERPINB8 (R88T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2223443	NM_002640.4(SERPINB8):c.839A>G (p.Glu280Gly)	SERPINB8 (E280G +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3160450	NM_002640.4(SERPINB8):c.851G>T (p.Arg284Leu)	SERPINB8 (R102L +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2351064	NM_002640.4(SERPINB8):c.851G>A (p.Arg284Gln)	SERPINB8 (R102Q +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2285243	NM_002640.4(SERPINB8):c.866T>C (p.Ile289Thr)	SERPINB8 (I107T +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 3160451	NM_002640.4(SERPINB8):c.868G>C (p.Asp290His)	SERPINB8 (D110H +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2293132	NM_002640.4(SERPINB8):c.918G>T (p.Lys306Asn)	SERPINB8 (K124N +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3160452	NM_002640.4(SERPINB8):c.935A>G (p.Lys312Arg)	SERPINB8 (K132R +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2283304	NM_002640.4(SERPINB8):c.973G>A (p.Gly325Ser)	SERPINB8 (G145S +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2272340	NM_002640.4(SERPINB8):c.973G>T (p.Gly325Cys)	SERPINB8 (G143C +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2152790	NM_002640.4(SERPINB8):c.988G>A (p.Ala330Thr)	SERPINB8 (A150T +2 more)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GUncertain significance
Select item 2333197	NM_002640.4(SERPINB8):c.1015C>T (p.Arg339Trp)	SERPINB8 (R159W +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3160444	NM_002640.4(SERPINB8):c.1022G>T (p.Ser341Ile)	SERPINB8 (S159I +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2240845	NM_002640.4(SERPINB8):c.1078C>T (p.His360Tyr)	SERPINB8 (H180Y +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2482531	NM_002640.4(SERPINB8):c.1093A>G (p.Ile365Val)	SERPINB8 (I185V +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2222288	NM_002640.4(SERPINB8):c.1109G>A (p.Arg370Lys)	SERPINB8 (R188K +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 32