"ANKRD26-related condition"[Disease/phenotype] AND "PreventionGenetics - ClinVar

Search results

Items: 81

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3036570	NM_014915.3(ANKRD26):c.5124T>C (p.Tyr1708=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 2519199	NM_014915.3(ANKRD26):c.4980A>G (p.Ile1660Met)	ANKRD26 (I1659M +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GUncertain significance
Select item 3043852	NM_014915.3(ANKRD26):c.4954-4dup	ANKRD26	Duplication (intron variant)	ANKRD26-related condition	GLikely benign
Select item 2636553	NM_014915.3(ANKRD26):c.4901C>A (p.Ser1634Tyr)	ANKRD26 (S1633Y +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 2629434	NM_014915.3(ANKRD26):c.4828C>A (p.Pro1610Thr)	ANKRD26 (P1609T +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 2885292	NM_014915.3(ANKRD26):c.4707G>A (p.Leu1569=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GLikely benign
Select item 2629759	NM_014915.3(ANKRD26):c.4590_4591delinsAAT (p.Lys1531fs)	ANKRD26 (K1530fs +1 more)	Indel (frameshift variant)	ANKRD26-related condition	GUncertain significance
Select item 2579772	NM_014915.3(ANKRD26):c.4564A>G (p.Met1522Val)	ANKRD26 (M1521V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2630295	NM_014915.3(ANKRD26):c.4534G>A (p.Glu1512Lys)	ANKRD26 (E1511K +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 432600	NM_014915.3(ANKRD26):c.4445T>C (p.Ile1482Thr)	ANKRD26 (I1482T +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 2635372	NM_014915.3(ANKRD26):c.4325A>T (p.Lys1442Met)	ANKRD26 (K1441M +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
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)	not provided +3 more	GBenign/Likely benign
Select item 2883638	NM_014915.3(ANKRD26):c.4128A>G (p.Glu1376=)	ANKRD26	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3044629	NM_014915.3(ANKRD26):c.4098C>T (p.Leu1366=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 2169140	NM_014915.3(ANKRD26):c.4078A>G (p.Ile1360Val)	ANKRD26 (I1360V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2716892	NM_014915.3(ANKRD26):c.4077G>A (p.Glu1359=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GLikely benign
Select item 3036354	NM_014915.3(ANKRD26):c.4060del (p.Val1354fs)	ANKRD26 (V1353fs +1 more)	Deletion (frameshift variant)	ANKRD26-related condition	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 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 3036216	NM_014915.3(ANKRD26):c.3705A>G (p.Gln1235=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 299734	NM_014915.3(ANKRD26):c.3655-4T>C	ANKRD26	Single nucleotide variant (intron variant)	ANKRD26-related condition +2 more	GBenign
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 1327670	NM_014915.3(ANKRD26):c.2855A>C (p.Lys952Thr)	ANKRD26 (K951T +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2634961	NM_014915.3(ANKRD26):c.2830G>T (p.Glu944Ter)	ANKRD26 (E943* +1 more)	Single nucleotide variant (nonsense)	ANKRD26-related condition	GUncertain significance
Select item 3031029	NM_014915.3(ANKRD26):c.2778A>G (p.Leu926=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 3061100	NM_014915.3(ANKRD26):c.2674G>T (p.Ala892Ser)	ANKRD26 (A891S +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 3030009	NM_014915.3(ANKRD26):c.2562C>T (p.Val854=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
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 2633626	NM_014915.3(ANKRD26):c.2536A>G (p.Thr846Ala)	ANKRD26 (T845A +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	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 2057309	NM_014915.3(ANKRD26):c.2421G>A (p.Thr807=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GLikely benign
Select item 2169160	NM_014915.3(ANKRD26):c.2403G>A (p.Lys801=)	ANKRD26	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2629936	NM_014915.3(ANKRD26):c.2279T>G (p.Val760Gly)	ANKRD26 (V759G +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +1 more	GUncertain significance
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 3031524	NM_014915.3(ANKRD26):c.2161+6del	ANKRD26	Deletion (intron variant)	ANKRD26-related condition	GLikely benign
Select item 2634021	NM_014915.3(ANKRD26):c.2083T>C (p.Ser695Pro)	ANKRD26 (S694P +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 2444878	NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)	ANKRD26 (D684N +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GConflicting classifications of pathogenicity
Select item 1314635	NM_014915.3(ANKRD26):c.1998A>G (p.Lys666=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GConflicting classifications of pathogenicity
Select item 877275	NM_014915.3(ANKRD26):c.1970A>T (p.Asp657Val)	ANKRD26 (D656V +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GConflicting classifications of pathogenicity
Select item 299743	NM_014915.3(ANKRD26):c.1868G>A (p.Arg623Gln)	ANKRD26 (R623Q +1 more)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GBenign
Select item 2080204	NM_014915.3(ANKRD26):c.1867C>T (p.Arg623Trp)	ANKRD26 (R622W +1 more)	Single nucleotide variant (missense variant)	not provided +1 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 1301008	NM_014915.3(ANKRD26):c.1728T>C (p.Asp576=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GBenign/Likely benign
Select item 3045501	NM_014915.3(ANKRD26):c.1611A>G (p.Glu537=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 2170612	NM_014915.3(ANKRD26):c.1565-4dup	ANKRD26	Duplication (intron variant)	ANKRD26-related condition +1 more	GBenign/Likely benign
Select item 3061272	NM_014915.3(ANKRD26):c.1462+4del	ANKRD26	Deletion (intron variant)	ANKRD26-related condition	GLikely benign
Select item 878895	NM_014915.3(ANKRD26):c.1364A>G (p.Asp455Gly)	ANKRD26 (D455G)	Single nucleotide variant (missense variant)	ANKRD26-related condition +2 more	GConflicting classifications of pathogenicity
Select item 3031142	NM_014915.3(ANKRD26):c.1364-5C>A	ANKRD26	Single nucleotide variant (intron variant)	ANKRD26-related condition	GLikely benign
Select item 1207046	NM_014915.3(ANKRD26):c.1269+11_1269+12del	ANKRD26	Deletion (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2628391	NM_014915.3(ANKRD26):c.1255C>T (p.Pro419Ser)	ANKRD26 (P419S)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 2635654	NM_014915.3(ANKRD26):c.1210A>G (p.Met404Val)	ANKRD26 (M404V)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 3054697	NM_014915.3(ANKRD26):c.1116T>C (p.Asn372=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition	GLikely benign
Select item 2635765	NM_014915.3(ANKRD26):c.1028TTC[1] (p.Leu344del)	ANKRD26 (L344del)	Microsatellite (inframe_deletion +1 more)	ANKRD26-related condition	GUncertain significance
Select item 299754	NM_014915.3(ANKRD26):c.948T>C (p.Asp316=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
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 2631290	NM_014915.3(ANKRD26):c.922G>C (p.Glu308Gln)	ANKRD26 (E308Q)	Single nucleotide variant (missense variant)	ANKRD26-related condition	GUncertain significance
Select item 299755	NM_014915.3(ANKRD26):c.874+8G>T	ANKRD26	Single nucleotide variant (intron variant)	ANKRD26-related condition +2 more	GBenign/Likely benign
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 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 2499686	NM_014915.3(ANKRD26):c.584T>C (p.Val195Ala)	ANKRD26 (V195A)	Single nucleotide variant (missense variant)	ANKRD26-related condition +1 more	GUncertain significance
Select item 434204	NM_014915.3(ANKRD26):c.542C>T (p.Thr181Ile)	ANKRD26 (T181I)	Single nucleotide variant (missense variant)	ANKRD26-related condition +3 more	GBenign/Likely benign
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 2712701	NM_014915.3(ANKRD26):c.333C>T (p.Asn111=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GLikely benign
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 2632497	NM_014915.3(ANKRD26):c.242+2T>C	ANKRD26	Single nucleotide variant (splice donor variant)	ANKRD26-related condition	GUncertain significance
Select item 2169715	NM_014915.3(ANKRD26):c.240C>T (p.Asn80=)	ANKRD26	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 more	GConflicting classifications of pathogenicity
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 2503379	NM_014915.3(ANKRD26):c.136G>A (p.Asp46Asn)	ANKRD26, LOC130003554 (D46N)	Single nucleotide variant (missense variant)	not provided +1 more	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 1312613	NM_014915.3(ANKRD26):c.105C>G (p.Tyr35Ter)	ANKRD26, LOC130003554 (Y35*)	Single nucleotide variant (nonsense)	not provided +1 more	GUncertain significance
Select item 299765	NM_014915.3(ANKRD26):c.93G>A (p.Gly31=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	ANKRD26-related condition +1 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 299766	NM_014915.3(ANKRD26):c.50C>T (p.Ala17Val)	ANKRD26, LOC130003554 (A17V)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +1 more	GUncertain significance
Select item 299768	NM_014915.3(ANKRD26):c.-113A>C	ANKRD26	Single nucleotide variant (5 prime UTR variant)	ANKRD26-related condition +3 more	GUncertain significance
Select item 1336159	NM_014915.3(ANKRD26):c.-117G>A	ANKRD26	Single nucleotide variant (5 prime UTR variant)	ANKRD26-related condition +2 more	GConflicting classifications of pathogenicity
Select item 3029759	NM_014915.3(ANKRD26):c.-135A>G	ANKRD26	Single nucleotide variant (5 prime UTR variant)	ANKRD26-related condition	GLikely benign
Select item 3060607	NM_014915.3(ANKRD26):c.-164C>T	ANKRD26	Single nucleotide variant (5 prime UTR variant)	ANKRD26-related condition	GLikely benign

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Items: 81