C4310621[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1027761	NM_012114.3(CASP14):c.328G>A (p.Glu110Lys)	CASP14 (E110K)	Single nucleotide variant (missense variant)	Ichthyosis, congenital, autosomal recessive 12	GUncertain significance
Select item 1027762	NM_012114.3(CASP14):c.332C>T (p.Ala111Val)	CASP14 (A111V)	Single nucleotide variant (missense variant)	Ichthyosis, congenital, autosomal recessive 12	GUncertain significance