"Ambry Genetics"[submitter] AND "SERPINA9"[gene] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3160361	NM_175739.4(SERPINA9):c.1250C>T (p.Ser417Phe)	SERPINA9 (S286F +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2555868	NM_175739.4(SERPINA9):c.1204A>G (p.Thr402Ala)	SERPINA9 (T271A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317571	NM_175739.4(SERPINA9):c.1168A>T (p.Asn390Tyr)	SERPINA9 (N290Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360796	NM_175739.4(SERPINA9):c.1133C>T (p.Ser378Leu)	SERPINA9 (S247L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160360	NM_175739.4(SERPINA9):c.1130G>A (p.Arg377Gln)	SERPINA9 (R246Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331442	NM_175739.4(SERPINA9):c.1115C>T (p.Thr372Ile)	SERPINA9 (T372I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317569	NM_175739.4(SERPINA9):c.1076T>C (p.Val359Ala)	SERPINA9 (V359A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616631	NM_175739.4(SERPINA9):c.1049A>C (p.Lys350Thr)	SERPINA9 (K219T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160359	NM_175739.4(SERPINA9):c.1042G>T (p.Val348Phe)	SERPINA9 (V217F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160357	NM_175739.4(SERPINA9):c.950A>G (p.Asn317Ser)	SERPINA9 (N317S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160369	NM_175739.4(SERPINA9):c.932C>T (p.Ser311Phe)	SERPINA9 (S211F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249353	NM_175739.4(SERPINA9):c.884G>C (p.Ser295Thr)	SERPINA9 (S215T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243356	NM_175739.4(SERPINA9):c.845T>G (p.Leu282Arg)	SERPINA9 (L151R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511218	NM_175739.4(SERPINA9):c.837G>C (p.Met279Ile)	SERPINA9 (M148I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473814	NM_175739.4(SERPINA9):c.781A>G (p.Met261Val)	SERPINA9 (M130V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529052	NM_175739.4(SERPINA9):c.779A>C (p.Gln260Pro)	SERPINA9 (Q160P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160368	NM_175739.4(SERPINA9):c.751G>A (p.Asp251Asn)	SERPINA9 (D151N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160367	NM_175739.4(SERPINA9):c.749T>C (p.Val250Ala)	SERPINA9 (V150A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381692	NM_175739.4(SERPINA9):c.720G>A (p.Met240Ile)	SERPINA9 (M109I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317575	NM_175739.4(SERPINA9):c.703G>T (p.Val235Leu)	SERPINA9 (V135L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259634	NM_175739.4(SERPINA9):c.662C>G (p.Thr221Arg)	SERPINA9 (T221R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218816	NM_175739.4(SERPINA9):c.636G>C (p.Trp212Cys)	SERPINA9 (W112C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317572	NM_175739.4(SERPINA9):c.610A>G (p.Asn204Asp)	SERPINA9 (N73D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238391	NM_175739.4(SERPINA9):c.593C>T (p.Thr198Met)	SERPINA9 (T67M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160366	NM_175739.4(SERPINA9):c.548C>T (p.Thr183Ile)	SERPINA9 (T103I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599076	NM_175739.4(SERPINA9):c.531C>G (p.Ser177Arg)	SERPINA9 (S177R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361466	NM_175739.4(SERPINA9):c.518C>A (p.Ala173Glu)	SERPINA9 (A173E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312822	NM_175739.4(SERPINA9):c.386C>G (p.Thr129Ser)	SERPINA9 (T49S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3160364	NM_175739.4(SERPINA9):c.290G>A (p.Gly97Asp)	SERPINA9 (G17D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522058	NM_175739.4(SERPINA9):c.229A>T (p.Thr77Ser)	SERPINA9 (T77S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3160363	NM_175739.4(SERPINA9):c.223G>A (p.Val75Ile)	SERPINA9 (V75I)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3317570	NM_175739.4(SERPINA9):c.200A>G (p.Asn67Ser)	SERPINA9 (N67S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472711	NM_175739.4(SERPINA9):c.194G>A (p.Ser65Asn)	SERPINA9 (S65N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2482124	NM_175739.4(SERPINA9):c.190C>G (p.Pro64Ala)	SERPINA9 (P64A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3317574	NM_175739.4(SERPINA9):c.174G>T (p.Arg58Ser)	SERPINA9 (R58S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2204342	NM_175739.4(SERPINA9):c.170G>A (p.Arg57His)	SERPINA9 (R57H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214541	NM_175739.4(SERPINA9):c.169C>T (p.Arg57Cys)	SERPINA9 (R57C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278402	NM_175739.4(SERPINA9):c.145A>C (p.Thr49Pro)	SERPINA9 (T49P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278401	NM_175739.4(SERPINA9):c.142A>C (p.Asn48His)	SERPINA9 (N48H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317568	NM_175739.4(SERPINA9):c.95G>A (p.Arg32His)	SERPINA9 (R32H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2410262	NM_175739.4(SERPINA9):c.56A>G (p.Tyr19Cys)	SERPINA9 (Y19C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160358	NM_175739.4(SERPINA9):c.47C>A (p.Ala16Asp)	SERPINA9 (A16D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386233	NM_175739.4(SERPINA9):c.-8G>A	SERPINA9	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 43