"Baylor Genetics"[submitter] AND "HYCC1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028966	NM_032581.4(HYCC1):c.461A>T (p.Gln154Leu)	HYCC1 (Q154L)	Single nucleotide variant (missense variant)	Hypomyelination and Congenital Cataract	GUncertain significance
Select item 1028965	NM_032581.4(HYCC1):c.262G>T (p.Ala88Ser)	HYCC1 (A88S)	Single nucleotide variant (missense variant)	Hypomyelination and Congenital Cataract	GUncertain significance