"Laboratory of Prof. Karen Avraham, Tel Aviv University"[submitter] AN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 917512	NM_001354587.1(ANKRD36):c.2479-1G>A	ANKRD36	Single nucleotide variant (splice acceptor variant)	Hearing loss, autosomal recessive	GLikely pathogenic
Select item 917513	NM_001354587.1(ANKRD36):c.2589T>G (p.Ser863Arg)	ANKRD36 (S863R)	Single nucleotide variant (missense variant)	Hearing loss, autosomal recessive	GLikely pathogenic