"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ANKRD55 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 719615	NM_024669.3(ANKRD55):c.1126T>C (p.Ser376Pro)	ANKRD55 (S376P)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 741976	NM_024669.3(ANKRD55):c.1052G>A (p.Cys351Tyr)	ANKRD55 (C351Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 785800	NM_024669.3(ANKRD55):c.835G>A (p.Glu279Lys)	ANKRD55 (E279K)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 787817	NM_024669.3(ANKRD55):c.723G>A (p.Ala241=)	ANKRD55	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 743566	NM_024669.3(ANKRD55):c.474G>A (p.Gln158=)	ANKRD55	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2424366	NC_000005.9:g.(?_52285299)_(56189507_?)del	ANKRD55, ARL15 +23 more	Deletion	not provided	GPathogenic

ClinVar