Related gene-specific medical variations for Gene (Select 22852) - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124261	NM_014915.3(ANKRD26):c.106T>G (p.Ser36Ala)	ANKRD26, LOC130003554 (S36A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2992559	NM_014915.3(ANKRD26):c.107C>A (p.Ser36Ter)	ANKRD26, LOC130003554 (S36*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2980853	NM_014915.3(ANKRD26):c.78C>A (p.Gly26=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906978	NM_014915.3(ANKRD26):c.82G>C (p.Gly28Arg)	ANKRD26, LOC130003554 (G28R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2905418	NM_014915.3(ANKRD26):c.109C>G (p.Gln37Glu)	ANKRD26, LOC130003554 (Q37E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2903477	NM_014915.3(ANKRD26):c.146A>G (p.Lys49Arg)	ANKRD26, LOC130003554 (K49R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2899976	NM_014915.3(ANKRD26):c.92G>A (p.Gly31Glu)	ANKRD26, LOC130003554 (G31E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2897933	NM_014915.3(ANKRD26):c.102C>T (p.Ala34=)	LOC130003554, ANKRD26	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893434	NM_014915.3(ANKRD26):c.26G>T (p.Gly9Val)	ANKRD26, LOC130003554 (G9V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2889642	NM_014915.3(ANKRD26):c.114C>G (p.Pro38=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2887763	NM_014915.3(ANKRD26):c.85G>A (p.Glu29Lys)	ANKRD26, LOC130003554 (E29K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2886688	NM_014915.3(ANKRD26):c.151C>T (p.His51Tyr)	ANKRD26, LOC130003554 (H51Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2886474	NM_014915.3(ANKRD26):c.93G>C (p.Gly31=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2886251	NM_014915.3(ANKRD26):c.24G>A (p.Lys8=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2885491	NM_014915.3(ANKRD26):c.79G>C (p.Gly27Arg)	ANKRD26, LOC130003554 (G27R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885021	NM_014915.3(ANKRD26):c.59_61del (p.Gln20del)	ANKRD26, LOC130003554 (Q20del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2884993	NM_014915.3(ANKRD26):c.114C>T (p.Pro38=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2884674	NM_014915.3(ANKRD26):c.89C>A (p.Pro30Gln)	ANKRD26, LOC130003554 (P30Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2825139	NM_014915.3(ANKRD26):c.22A>C (p.Lys8Gln)	ANKRD26, LOC130003554 (K8Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2822190	NM_014915.3(ANKRD26):c.-3_-2delinsCA	ANKRD26, LOC130003554	Indel (5 prime UTR variant)	not provided	GUncertain significance
Select item 2737825	NM_014915.3(ANKRD26):c.81_101dup (p.Ala34_Tyr35insGlyGluProGlyGluGlyAla)	ANKRD26, LOC130003554	Duplication (inframe_insertion)	not provided	GUncertain significance
Select item 2707940	NM_014915.3(ANKRD26):c.74G>C (p.Gly25Ala)	ANKRD26, LOC130003554 (G25A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2676724	NM_014915.3(ANKRD26):c.3589A>C (p.Ile1197Leu)	ANKRD26 (I1196L +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2	GUncertain significance
Select item 2627083	NM_014915.3(ANKRD26):c.4155T>A (p.His1385Gln)	ANKRD26 (H1384Q +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2	GUncertain significance
Select item 2578185	NM_014915.3(ANKRD26):c.104A>T (p.Tyr35Phe)	ANKRD26, LOC130003554 (Y35F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578065	NM_014915.3(ANKRD26):c.-2C>G	ANKRD26, LOC130003554	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 2574353	NM_014915.3(ANKRD26):c.142G>A (p.Gly48Ser)	ANKRD26, LOC130003554 (G48S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2499322	NM_014915.3(ANKRD26):c.56G>T (p.Arg19Leu)	ANKRD26, LOC130003554 (R19L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
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 2429700	NM_014915.3(ANKRD26):c.66C>A (p.Ser22Arg)	ANKRD26, LOC130003554 (S22R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2429548	NM_014915.3(ANKRD26):c.31T>A (p.Ser11Thr)	ANKRD26, LOC130003554 (S11T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2397743	NM_014915.3(ANKRD26):c.17G>T (p.Ser6Ile)	ANKRD26, LOC130003554 (S6I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2178858	NM_014915.3(ANKRD26):c.72G>A (p.Ala24=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2173220	NM_014915.3(ANKRD26):c.79G>T (p.Gly27Trp)	ANKRD26, LOC130003554 (G27W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2169379	NM_014915.3(ANKRD26):c.141C>T (p.Leu47=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2167419	NM_014915.3(ANKRD26):c.96G>C (p.Glu32Asp)	ANKRD26, LOC130003554 (E32D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2077850	NM_014915.3(ANKRD26):c.108G>C (p.Ser36=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1954767	NM_014915.3(ANKRD26):c.-9G>T	ANKRD26, LOC130003554	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
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 1337772	NM_014915.3(ANKRD26):c.110A>G (p.Gln37Arg)	ANKRD26, LOC130003554 (Q37R)	Single nucleotide variant (missense variant)	ANKRD26-related disorder +2 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 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 1311901	NM_014915.3(ANKRD26):c.121C>T (p.His41Tyr)	ANKRD26, LOC130003554 (H41Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1304129	NM_014915.3(ANKRD26):c.26G>A (p.Gly9Asp)	ANKRD26, LOC130003554 (G9D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1049678	NM_014915.3(ANKRD26):c.98G>T (p.Gly33Val)	ANKRD26, LOC130003554 (G33V)	Single nucleotide variant (missense variant)	not provided	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 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 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 450395	NM_014915.3(ANKRD26):c.112C>T (p.Pro38Ser)	ANKRD26, LOC130003554 (P38S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 434205	NM_014915.3(ANKRD26):c.92G>C (p.Gly31Ala)	LOC130003554, ANKRD26 (G31A)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +4 more	GConflicting classifications of pathogenicity
Select item 299767	NM_014915.3(ANKRD26):c.-4G>A	ANKRD26, LOC130003554	Single nucleotide variant (5 prime UTR variant)	Thrombocytopenia 2 +1 more	GUncertain significance
Select item 299766	NM_014915.3(ANKRD26):c.50C>T (p.Ala17Val)	ANKRD26, LOC130003554 (A17V)	Single nucleotide variant (missense variant)	ANKRD26-related disorder +1 more	GUncertain significance
Select item 299765	NM_014915.3(ANKRD26):c.93G>A (p.Gly31=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	Thrombocytopenia 2 +1 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 299763	NM_014915.3(ANKRD26):c.162C>T (p.Ala54=)	ANKRD26, LOC130003554	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 260472	NM_014915.3(ANKRD26):c.59A>G (p.Gln20Arg)	ANKRD26, LOC130003554 (Q20R)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 260456	NM_014915.3(ANKRD26):c.1269+7_1269+12delinsA	ANKRD26	Indel (intron variant)	not specified	GLikely benign
Select item 221473	GRCh37/hg19 10p12.1(chr10:27326892-27356151)x3	ANKRD26	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance
Select item 210181	NM_014915.3(ANKRD26):c.153C>G (p.His51Gln)	ANKRD26, LOC130003554 (H51Q)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +3 more	GConflicting classifications of pathogenicity

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Items: 60