"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZMYND10"[ - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2195423	NM_015896.4(ZMYND10):c.1121+10G>A	ZMYND10	Single nucleotide variant (intron variant)	ZMYND10-related disorder +1 more	GLikely benign
Select item 2195466	NM_015896.4(ZMYND10):c.1115C>T (p.Ala372Val)	ZMYND10 (A372V +1 more)	Single nucleotide variant (missense variant)	ZMYND10-related disorder +1 more	GLikely benign
Select item 525561	NM_015896.4(ZMYND10):c.999+7A>T	ZMYND10	Single nucleotide variant (intron variant)	ZMYND10-related disorder +1 more	GLikely benign
Select item 454844	NM_015896.4(ZMYND10):c.873+4A>T	ZMYND10	Single nucleotide variant (intron variant)	ZMYND10-related disorder +1 more	GBenign
Select item 1457875	NM_015896.4(ZMYND10):c.709C>T (p.Gln237Ter)	ZMYND10 (Q232* +1 more)	Single nucleotide variant (nonsense)	Primary ciliary dyskinesia +1 more	GPathogenic/Likely pathogenic
Select item 3043014	NM_015896.4(ZMYND10):c.701-33G>A	ZMYND10 (R218H)	Single nucleotide variant (missense variant +1 more)	ZMYND10-related disorder	GLikely benign
Select item 2631568	NM_015896.4(ZMYND10):c.668dup (p.Glu224fs)	ZMYND10 (E224fs)	Duplication (frameshift variant +1 more)	ZMYND10-related disorder	GLikely pathogenic
Select item 66022	NM_015896.4(ZMYND10):c.300del (p.Phe101fs)	ZMYND10 (F101fs)	Deletion (frameshift variant)	ZMYND10-related disorder +1 more	GPathogenic
Select item 410633	NM_015896.4(ZMYND10):c.229G>A (p.Ala77Thr)	ZMYND10 (A77T)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +2 more	GConflicting classifications of pathogenicity