"Genetic Services Laboratory, University of Chicago"[submitter] AND "A - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1338099	NM_014915.3(ANKRD26):c.*6A>G	ANKRD26	Single nucleotide variant (3 prime UTR variant)	not specified	GUncertain significance
Select item 1338438	NM_014915.3(ANKRD26):c.4953+1G>T	ANKRD26	Single nucleotide variant (splice donor variant)	not specified	GUncertain significance
Select item 1211918	NM_014915.3(ANKRD26):c.4916G>A (p.Arg1639Gln)	ANKRD26 (R1638Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1337901	NM_014915.3(ANKRD26):c.4876A>C (p.Ile1626Leu)	ANKRD26 (I1625L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1337389	NM_014915.3(ANKRD26):c.4724+11A>G	ANKRD26	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 1338229	NM_014915.3(ANKRD26):c.4724+2T>A	ANKRD26	Single nucleotide variant (splice donor variant)	not specified	GUncertain significance
Select item 1337060	NM_014915.3(ANKRD26):c.4715A>G (p.Lys1572Arg)	ANKRD26 (K1571R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 434206	NM_014915.3(ANKRD26):c.4636G>C (p.Asp1546His)	ANKRD26 (D1546H +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +3 more	GConflicting classifications of pathogenicity
Select item 1337531	NM_014915.3(ANKRD26):c.4507G>T (p.Ala1503Ser)	ANKRD26 (A1502S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 877210	NM_014915.3(ANKRD26):c.4490T>A (p.Val1497Asp)	ANKRD26 (V1496D +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 1338659	NM_014915.3(ANKRD26):c.4342del (p.Gln1448fs)	ANKRD26 (Q1447fs +1 more)	Deletion (frameshift variant)	not specified	GUncertain significance
Select item 434207	NM_014915.3(ANKRD26):c.4336A>G (p.Lys1446Glu)	ANKRD26 (K1446E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1336420	NM_014915.3(ANKRD26):c.4299G>A (p.Glu1433=)	ANKRD26	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 210184	NM_014915.3(ANKRD26):c.4259G>A (p.Cys1420Tyr)	ANKRD26 (C1420Y +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +3 more	GBenign/Likely benign
Select item 299731	NM_014915.3(ANKRD26):c.4188T>C (p.Asp1396=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +3 more	GBenign/Likely benign
Select item 260469	NM_014915.3(ANKRD26):c.4145T>A (p.Phe1382Tyr)	ANKRD26 (F1382Y +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 434208	NM_014915.3(ANKRD26):c.4125T>G (p.Asn1375Lys)	ANKRD26 (N1375K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1338119	NM_014915.3(ANKRD26):c.4121T>C (p.Leu1374Ser)	ANKRD26 (L1373S +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1337621	NM_014915.3(ANKRD26):c.4109C>T (p.Thr1370Ile)	ANKRD26 (T1369I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1337931	NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly)	ANKRD26 (D1253G +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +3 more	GConflicting classifications of pathogenicity
Select item 1337578	NM_014915.3(ANKRD26):c.3739C>T (p.Arg1247Cys)	ANKRD26 (R1246C +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1301264	NM_014915.3(ANKRD26):c.3735G>A (p.Thr1245=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
Select item 1337895	NM_014915.3(ANKRD26):c.3710T>C (p.Met1237Thr)	ANKRD26 (M1236T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 299733	NM_014915.3(ANKRD26):c.3704A>T (p.Gln1235Leu)	ANKRD26 (Q1235L +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 930454	NM_014915.3(ANKRD26):c.3686C>T (p.Ala1229Val)	ANKRD26 (A1229V +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1050113	NM_014915.3(ANKRD26):c.3661G>A (p.Val1221Met)	ANKRD26 (V1220M +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 878252	NM_014915.3(ANKRD26):c.3655G>A (p.Val1219Ile)	ANKRD26 (V1218I +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 299736	NM_014915.3(ANKRD26):c.3286C>T (p.Arg1096Trp)	ANKRD26 (R1096W +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +3 more	GConflicting classifications of pathogenicity
Select item 777851	NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys)	ANKRD26 (E1002K +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 452061	NM_014915.3(ANKRD26):c.2902A>G (p.Thr968Ala)	ANKRD26 (T968A +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1336593	NM_014915.3(ANKRD26):c.2807A>G (p.Gln936Arg)	ANKRD26 (Q935R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 880061	NM_014915.3(ANKRD26):c.2697+9A>G	ANKRD26	Single nucleotide variant (intron variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 260463	NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)	ANKRD26	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 880062	NM_014915.3(ANKRD26):c.2584C>G (p.Gln862Glu)	ANKRD26 (Q861E +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 299739	NM_014915.3(ANKRD26):c.2559+10T>A	ANKRD26	Single nucleotide variant (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1337722	NM_014915.3(ANKRD26):c.2559+3A>G	ANKRD26	Single nucleotide variant (intron variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
Select item 1337782	NM_014915.3(ANKRD26):c.2539G>C (p.Val847Leu)	ANKRD26 (V846L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 434209	NM_014915.3(ANKRD26):c.2524A>G (p.Met842Val)	ANKRD26 (M842V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1338280	NM_014915.3(ANKRD26):c.2458G>C (p.Glu820Gln)	ANKRD26 (E819Q +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GUncertain significance
Select item 1336062	NM_014915.3(ANKRD26):c.2420C>T (p.Thr807Met)	ANKRD26 (T806M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 434202	NM_014915.3(ANKRD26):c.2332G>C (p.Glu778Gln)	ANKRD26 (E778Q +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 717238	NM_014915.3(ANKRD26):c.2170A>C (p.Ser724Arg)	ANKRD26 (S723R +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1337206	NM_014915.3(ANKRD26):c.2162-12T>C	ANKRD26	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 1337764	NM_014915.3(ANKRD26):c.2151G>A (p.Met717Ile)	ANKRD26 (M716I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1338187	NM_014915.3(ANKRD26):c.2078C>T (p.Thr693Ile)	ANKRD26 (T692I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1337875	NM_014915.3(ANKRD26):c.2048A>G (p.Asp683Gly)	ANKRD26 (D682G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 877274	NM_014915.3(ANKRD26):c.2005A>G (p.Asn669Asp)	ANKRD26 (N668D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 1336163	NM_014915.3(ANKRD26):c.1835T>C (p.Met612Thr)	ANKRD26 (M611T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1312615	NM_001256053.2(ANKRD26):c.1815-2_1815del	ANKRD26	Microsatellite (splice acceptor variant)	not provided	GConflicting classifications of pathogenicity
Select item 723707	NM_014915.3(ANKRD26):c.1806G>A (p.Glu602=)	ANKRD26	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1193048	NM_014915.3(ANKRD26):c.1790G>C (p.Arg597Thr)	ANKRD26 (R597T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 878314	NM_014915.3(ANKRD26):c.1747C>G (p.Gln583Glu)	ANKRD26 (Q583E)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 299745	NM_014915.3(ANKRD26):c.1635+9T>C	ANKRD26	Single nucleotide variant (intron variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 434212	NM_014915.3(ANKRD26):c.1619A>C (p.Glu540Ala)	ANKRD26 (E540A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 260460	NM_014915.3(ANKRD26):c.1590AGA[2] (p.Glu533del)	ANKRD26 (E533del)	Microsatellite (inframe_deletion)	Thrombocytopenia +3 more	GBenign/Likely benign
Select item 210182	NM_014915.3(ANKRD26):c.1571A>G (p.His524Arg)	ANKRD26 (H524R)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GBenign
Select item 714308	NM_014915.3(ANKRD26):c.1451T>C (p.Val484Ala)	ANKRD26 (V484A)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1338601	NM_014915.3(ANKRD26):c.1363+1G>T	ANKRD26	Single nucleotide variant (splice donor variant)	not specified	GUncertain significance
Select item 2443165	NM_014915.3(ANKRD26):c.1340A>G (p.Asn447Ser)	ANKRD26 (N447S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 878896	NM_014915.3(ANKRD26):c.1327G>A (p.Gly443Arg)	ANKRD26 (G443R)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GUncertain significance
Select item 1337884	NM_014915.3(ANKRD26):c.1269+10A>G	ANKRD26	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 1338447	NM_014915.3(ANKRD26):c.1269+3A>G	ANKRD26	Single nucleotide variant (intron variant)	not specified +1 more	GUncertain significance
Select item 1336697	NM_014915.3(ANKRD26):c.1208-3T>C	ANKRD26	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 299752	NM_014915.3(ANKRD26):c.1153A>G (p.Thr385Ala)	ANKRD26 (T385A)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 712487	NM_014915.3(ANKRD26):c.1133A>G (p.Glu378Gly)	ANKRD26 (E378G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 1338545	NM_014915.3(ANKRD26):c.1110dup (p.Glu371fs)	ANKRD26 (E371fs)	Duplication (frameshift variant)	not specified	GUncertain significance
Select item 1337753	NM_014915.3(ANKRD26):c.945A>G (p.Gln315=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
Select item 1336378	NM_014915.3(ANKRD26):c.937G>T (p.Asp313Tyr)	ANKRD26 (D313Y)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
Select item 1338071	NM_014915.3(ANKRD26):c.826C>T (p.Pro276Ser)	ANKRD26 (P276S)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1336586	NM_014915.3(ANKRD26):c.770C>T (p.Ser257Leu)	ANKRD26 (S257L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 880123	NM_014915.3(ANKRD26):c.756G>A (p.Pro252=)	ANKRD26	Single nucleotide variant (synonymous variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 1337501	NM_014915.3(ANKRD26):c.710T>C (p.Val237Ala)	ANKRD26 (V237A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2443159	NM_014915.3(ANKRD26):c.710-6T>C	ANKRD26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1337898	NM_014915.3(ANKRD26):c.697A>G (p.Asn233Asp)	ANKRD26 (N233D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 877327	NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser)	ANKRD26 (P227S)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 434203	NM_014915.3(ANKRD26):c.678A>T (p.Ile226=)	ANKRD26	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 1337300	NM_014915.3(ANKRD26):c.599A>G (p.Lys200Arg)	ANKRD26 (K200R)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GConflicting classifications of pathogenicity
Select item 434204	NM_014915.3(ANKRD26):c.542C>T (p.Thr181Ile)	ANKRD26 (T181I)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +3 more	GBenign/Likely benign
Select item 299759	NM_014915.3(ANKRD26):c.531+10A>T	ANKRD26	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 877329	NM_014915.3(ANKRD26):c.531+9C>G	ANKRD26	Single nucleotide variant (intron variant)	Thrombocytopenia 2 +2 more	GBenign
Select item 1336594	NM_014915.3(ANKRD26):c.513T>C (p.Asn171=)	ANKRD26	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1033718	NM_014915.3(ANKRD26):c.371A>T (p.Gln124Leu)	ANKRD26 (Q124L)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1338468	NM_014915.3(ANKRD26):c.349C>G (p.Leu117Val)	ANKRD26 (L117V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2443175	NM_014915.3(ANKRD26):c.329A>G (p.Asp110Gly)	ANKRD26 (D110G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1338157	NM_014915.3(ANKRD26):c.320A>G (p.Asn107Ser)	ANKRD26 (N107S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1336709	NM_014915.3(ANKRD26):c.301G>A (p.Asp101Asn)	ANKRD26 (D101N)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GConflicting classifications of pathogenicity
Select item 1337489	NM_014915.3(ANKRD26):c.267C>T (p.Ala89=)	ANKRD26	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 210183	NM_014915.3(ANKRD26):c.243-85_243-76del	ANKRD26	Deletion (intron variant)	not specified	GUncertain significance
Select item 210181	NM_014915.3(ANKRD26):c.153C>G (p.His51Gln)	ANKRD26, LOC130003554 (H51Q)	Single nucleotide variant (missense variant)	ANKRD26-related condition +3 more	GConflicting classifications of pathogenicity
Select item 878357	NM_014915.3(ANKRD26):c.141C>A (p.Leu47=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 2443161	NM_014915.3(ANKRD26):c.133C>T (p.Arg45Ter)	ANKRD26, LOC130003554 (R45*)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 450395	NM_014915.3(ANKRD26):c.112C>T (p.Pro38Ser)	ANKRD26, LOC130003554 (P38S)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1337772	NM_014915.3(ANKRD26):c.110A>G (p.Gln37Arg)	LOC130003554, ANKRD26 (Q37R)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GConflicting classifications of pathogenicity
Select item 299764	NM_014915.3(ANKRD26):c.101C>T (p.Ala34Val)	ANKRD26, LOC130003554 (A34V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 434205	NM_014915.3(ANKRD26):c.92G>C (p.Gly31Ala)	ANKRD26, LOC130003554 (G31A)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +4 more	GConflicting classifications of pathogenicity
Select item 1337051	NM_014915.3(ANKRD26):c.83G>T (p.Gly28Val)	ANKRD26, LOC130003554 (G28V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712488	NM_014915.3(ANKRD26):c.40G>A (p.Gly14Ser)	ANKRD26, LOC130003554 (G14S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 1338151	NM_014915.3(ANKRD26):c.20A>G (p.Lys7Arg)	ANKRD26, LOC130003554 (K7R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 878948	NM_014915.3(ANKRD26):c.3G>A (p.Met1Ile)	ANKRD26, LOC130003554 (M1I)	Single nucleotide variant (missense variant +1 more)	Thrombocytopenia 2 +2 more	GConflicting classifications of pathogenicity
Select item 1336078	NM_014915.3(ANKRD26):c.-53C>T	ANKRD26	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance

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