"GeneDx"[submitter] AND "ZMYND10"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57771	GRCh38/hg38 3p21.31-14.3(chr3:49461000-55314500)x1	ABHD14A, ABHD14A-ACY1 +329 more	Copy number loss	See cases	GPathogenic
Select item 1221244	NM_015896.4(ZMYND10):c.*213T>C	ZMYND10	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1193297	NM_015896.4(ZMYND10):c.*134G>T	ZMYND10	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 1231903	NM_015896.4(ZMYND10):c.1248-30T>C	ZMYND10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 241067	NM_015896.4(ZMYND10):c.1105C>T (p.Arg369Trp)	ZMYND10 (R369W +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +1 more	GBenign/Likely benign
Select item 241066	NM_015896.4(ZMYND10):c.1073A>G (p.Gln358Arg)	ZMYND10 (Q358R +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 22 +2 more	GBenign/Likely benign
Select item 241073	NM_015896.4(ZMYND10):c.970C>A (p.Pro324Thr)	ZMYND10 (P324T +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +1 more	GBenign/Likely benign
Select item 1438577	NM_015896.4(ZMYND10):c.778G>A (p.Gly260Arg)	ZMYND10 (G255R +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +2 more	GConflicting classifications of pathogenicity
Select item 1245716	NM_015896.4(ZMYND10):c.511-24C>T	ZMYND10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 241069	NM_015896.4(ZMYND10):c.478G>A (p.Gly160Arg)	ZMYND10 (G160R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign