"Genetics and Molecular Pathology, SA Pathology"[submitter] AND "ANKRD - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 432600	NM_014915.3(ANKRD26):c.4445T>C (p.Ile1482Thr)	ANKRD26 (I1482T +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +2 more	GBenign/Likely benign
Select item 777851	NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys)	ANKRD26 (E1002K +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 717238	NM_014915.3(ANKRD26):c.2170A>C (p.Ser724Arg)	ANKRD26 (S723R +1 more)	Single nucleotide variant (missense variant)	Thrombocytopenia 2 +3 more	GConflicting classifications of pathogenicity
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 627410	NM_014915.3(ANKRD26):c.-118C>T	ANKRD26	Single nucleotide variant (5 prime UTR variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 30853	NM_014915.3(ANKRD26):c.-134G>A	ANKRD26	Single nucleotide variant (5 prime UTR variant)	not provided +2 more	GPathogenic/Likely pathogenic

ClinVar