"Ambry Genetics"[submitter] AND "BIRC6"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623439	NM_016252.4(BIRC6):c.10G>T (p.Gly4Cys)	BIRC6 (G4C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228199	NM_016252.4(BIRC6):c.19G>A (p.Ala7Thr)	BIRC6 (A7T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609142	NM_016252.4(BIRC6):c.23C>T (p.Ala8Val)	BIRC6 (A8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134097	NM_016252.4(BIRC6):c.80G>A (p.Arg27Gln)	BIRC6, LOC129933458 (R27Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2514158	NM_016252.4(BIRC6):c.118G>C (p.Gly40Arg)	BIRC6, LOC129933458 (G12R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134059	NM_016252.4(BIRC6):c.160G>C (p.Glu54Gln)	BIRC6, LOC129933458 (E54Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134061	NM_016252.4(BIRC6):c.182G>A (p.Gly61Asp)	BIRC6, LOC129933458 (G33D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389242	NM_016252.4(BIRC6):c.499G>A (p.Val167Ile)	BIRC6 (V167I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260959	NM_016252.4(BIRC6):c.544G>A (p.Asp182Asn)	BIRC6 (D182N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260968	NM_016252.4(BIRC6):c.800G>A (p.Arg267His)	BIRC6 (R239H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374028	NM_016252.4(BIRC6):c.952C>G (p.Pro318Ala)	BIRC6 (P318A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226303	NM_016252.4(BIRC6):c.997G>A (p.Val333Ile)	BIRC6 (V305I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134040	NM_016252.4(BIRC6):c.1178C>T (p.Ser393Leu)	BIRC6 (S365L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134046	NM_016252.4(BIRC6):c.1247A>G (p.Lys416Arg)	BIRC6 (K388R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317299	NM_016252.4(BIRC6):c.1328C>T (p.Pro443Leu)	BIRC6 (P415L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239879	NM_016252.4(BIRC6):c.1330A>C (p.Ser444Arg)	BIRC6 (S416R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335232	NM_016252.4(BIRC6):c.1441G>C (p.Asp481His)	BIRC6 (D481H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134060	NM_016252.4(BIRC6):c.1621A>C (p.Asn541His)	BIRC6 (N513H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339231	NM_016252.4(BIRC6):c.1646G>A (p.Ser549Asn)	BIRC6 (S549N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354324	NM_016252.4(BIRC6):c.1814A>G (p.Gln605Arg)	BIRC6 (Q577R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134062	NM_016252.4(BIRC6):c.1881A>C (p.Leu627Phe)	BIRC6 (L599F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134063	NM_016252.4(BIRC6):c.1963A>C (p.Lys655Gln)	BIRC6 (K627Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134064	NM_016252.4(BIRC6):c.1982G>C (p.Gly661Ala)	BIRC6 (G633A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248726	NM_016252.4(BIRC6):c.2091C>A (p.Asn697Lys)	BIRC6 (N697K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134065	NM_016252.4(BIRC6):c.2225G>A (p.Gly742Glu)	BIRC6 (G714E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134066	NM_016252.4(BIRC6):c.2233T>G (p.Leu745Val)	BIRC6 (L745V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605788	NM_016252.4(BIRC6):c.2372T>C (p.Val791Ala)	BIRC6 (V763A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260974	NM_016252.4(BIRC6):c.2428C>G (p.Pro810Ala)	BIRC6 (P810A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326806	NM_016252.4(BIRC6):c.2471A>G (p.Tyr824Cys)	BIRC6 (Y824C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375481	NM_016252.4(BIRC6):c.2549A>G (p.Lys850Arg)	BIRC6 (K850R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2628777	NM_016252.4(BIRC6):c.2558A>G (p.Gln853Arg)	BIRC6 (Q825R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2611156	NM_016252.4(BIRC6):c.2566A>G (p.Ile856Val)	BIRC6 (I856V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288802	NM_016252.4(BIRC6):c.2578A>G (p.Ile860Val)	BIRC6 (I832V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514368	NM_016252.4(BIRC6):c.2632A>G (p.Ile878Val)	BIRC6 (I850V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3260973	NM_016252.4(BIRC6):c.2659A>G (p.Asn887Asp)	BIRC6 (N859D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216124	NM_016252.4(BIRC6):c.2906C>A (p.Thr969Asn)	BIRC6 (T969N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533324	NM_016252.4(BIRC6):c.2909G>T (p.Cys970Phe)	BIRC6 (C970F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611717	NM_016252.4(BIRC6):c.2933T>C (p.Ile978Thr)	BIRC6 (I978T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134067	NM_016252.4(BIRC6):c.2977G>C (p.Glu993Gln)	BIRC6 (E993Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134068	NM_016252.4(BIRC6):c.3088C>T (p.Arg1030Cys)	BIRC6 (R1030C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623686	NM_016252.4(BIRC6):c.3320A>G (p.Lys1107Arg)	BIRC6 (K1079R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260970	NM_016252.4(BIRC6):c.3325G>C (p.Val1109Leu)	BIRC6 (V1081L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598202	NM_016252.4(BIRC6):c.3347A>G (p.Asn1116Ser)	BIRC6 (N1116S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302423	NM_016252.4(BIRC6):c.3352C>T (p.Pro1118Ser)	BIRC6 (P1090S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281187	NM_016252.4(BIRC6):c.3398G>A (p.Gly1133Glu)	BIRC6 (G1133E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594750	NM_016252.4(BIRC6):c.3446C>T (p.Ser1149Phe)	BIRC6 (S1135F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134069	NM_016252.4(BIRC6):c.3461A>G (p.Asn1154Ser)	BIRC6 (N1154S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134070	NM_016252.4(BIRC6):c.3506G>T (p.Arg1169Ile)	BIRC6 (R1155I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134071	NM_016252.4(BIRC6):c.3507A>T (p.Arg1169Ser)	BIRC6 (R1155S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134072	NM_016252.4(BIRC6):c.3556G>A (p.Val1186Ile)	BIRC6 (V1172I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280773	NM_016252.4(BIRC6):c.3671T>C (p.Val1224Ala)	BIRC6 (V1224A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134073	NM_016252.4(BIRC6):c.3692G>A (p.Gly1231Glu)	BIRC6 (G1231E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238523	NM_016252.4(BIRC6):c.4015A>C (p.Thr1339Pro)	BIRC6 (T1325P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219009	NM_016252.4(BIRC6):c.4152T>A (p.Phe1384Leu)	BIRC6 (F1384L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270195	NM_016252.4(BIRC6):c.4162A>G (p.Ile1388Val)	BIRC6 (I1388V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318723	NM_016252.4(BIRC6):c.4169G>A (p.Arg1390His)	BIRC6 (R1390H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302981	NM_016252.4(BIRC6):c.4462A>G (p.Met1488Val)	BIRC6 (M1488V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245297	NM_016252.4(BIRC6):c.4490G>T (p.Gly1497Val)	BIRC6 (G1497V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134075	NM_016252.4(BIRC6):c.4682T>C (p.Leu1561Ser)	BIRC6 (L1547S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233404	NM_016252.4(BIRC6):c.4705A>T (p.Thr1569Ser)	BIRC6 (T1569S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348885	NM_016252.4(BIRC6):c.4934A>G (p.Gln1645Arg)	BIRC6 (Q1645R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406186	NM_016252.4(BIRC6):c.5015T>C (p.Val1672Ala)	BIRC6 (V1672A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260966	NM_016252.4(BIRC6):c.5170C>T (p.Leu1724Phe)	BIRC6 (L1714F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134076	NM_016252.4(BIRC6):c.5177A>G (p.Gln1726Arg)	BIRC6 (Q1716R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339538	NM_016252.4(BIRC6):c.5189G>C (p.Gly1730Ala)	BIRC6 (G1720A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134077	NM_016252.4(BIRC6):c.5198T>C (p.Ile1733Thr)	BIRC6 (I1733T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483707	NM_016252.4(BIRC6):c.5228A>C (p.His1743Pro)	BIRC6 (H1733P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538596	NM_016252.4(BIRC6):c.5248T>C (p.Ser1750Pro)	BIRC6 (S1740P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134078	NM_016252.4(BIRC6):c.5260C>G (p.Pro1754Ala)	BIRC6 (P1754A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134079	NM_016252.4(BIRC6):c.5434T>G (p.Leu1812Val)	BIRC6 (L1802V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527747	NM_016252.4(BIRC6):c.5541A>C (p.Leu1847Phe)	BIRC6 (L1837F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618744	NM_016252.4(BIRC6):c.5542A>G (p.Ile1848Val)	BIRC6 (I1838V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218479	NM_016252.4(BIRC6):c.5642A>G (p.His1881Arg)	BIRC6 (H1881R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520888	NM_016252.4(BIRC6):c.5762A>G (p.Gln1921Arg)	BIRC6 (Q1921R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309187	NM_016252.4(BIRC6):c.5800C>T (p.Arg1934Cys)	BIRC6 (R1924C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368217	NM_016252.4(BIRC6):c.5824A>G (p.Ile1942Val)	BIRC6 (I1942V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134080	NM_016252.4(BIRC6):c.5846G>A (p.Ser1949Asn)	BIRC6 (S1949N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134081	NM_016252.4(BIRC6):c.5863T>A (p.Tyr1955Asn)	BIRC6 (Y1945N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518706	NM_016252.4(BIRC6):c.5878C>G (p.Pro1960Ala)	BIRC6 (P1950A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134082	NM_016252.4(BIRC6):c.5890G>A (p.Val1964Ile)	BIRC6 (V1954I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227931	NM_016252.4(BIRC6):c.6005G>A (p.Arg2002Gln)	BIRC6 (R2002Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529256	NM_016252.4(BIRC6):c.6058A>C (p.Thr2020Pro)	BIRC6 (T2010P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134083	NM_016252.4(BIRC6):c.6073A>G (p.Thr2025Ala)	BIRC6 (T2025A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478119	NM_016252.4(BIRC6):c.6155G>A (p.Ser2052Asn)	BIRC6 (S2052N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234447	NM_016252.4(BIRC6):c.6170A>G (p.Gln2057Arg)	BIRC6 (Q2047R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375910	NM_016252.4(BIRC6):c.6232A>G (p.Thr2078Ala)	BIRC6 (T2078A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300949	NM_016252.4(BIRC6):c.6430A>G (p.Asn2144Asp)	BIRC6 (N2144D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134085	NM_016252.4(BIRC6):c.6511G>A (p.Val2171Ile)	BIRC6 (V2161I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260961	NM_016252.4(BIRC6):c.6569C>T (p.Ala2190Val)	BIRC6 (A2190V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134086	NM_016252.4(BIRC6):c.6574G>T (p.Ala2192Ser)	BIRC6 (A2182S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251343	NM_016252.4(BIRC6):c.6620A>G (p.Asn2207Ser)	BIRC6 (N2206S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134087	NM_016252.4(BIRC6):c.6627C>G (p.His2209Gln)	BIRC6 (H2209Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599944	NM_016252.4(BIRC6):c.6662G>A (p.Ser2221Asn)	BIRC6 (S2220N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281092	NM_016252.4(BIRC6):c.6772A>C (p.Lys2258Gln)	BIRC6 (K2258Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260967	NM_016252.4(BIRC6):c.6825A>C (p.Gln2275His)	BIRC6 (Q2274H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260956	NM_016252.4(BIRC6):c.6902C>T (p.Ser2301Phe)	BIRC6 (S2301F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257827	NM_016252.4(BIRC6):c.6917A>G (p.Glu2306Gly)	BIRC6 (E2306G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134089	NM_016252.4(BIRC6):c.6940C>A (p.Pro2314Thr)	BIRC6 (P2313T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258313	NM_016252.4(BIRC6):c.6980G>A (p.Arg2327His)	BIRC6 (R2327H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134090	NM_016252.4(BIRC6):c.7105A>G (p.Ile2369Val)	BIRC6 (I2368V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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