C4225382[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 787174	NM_014822.4(SEC24D):c.1576C>T (p.Leu526Phe)	SEC24D (L526F +1 more)	Single nucleotide variant (missense variant)	Cole-Carpenter syndrome 2 +1 more	GBenign/Likely benign
Select item 1303509	NM_014822.4(SEC24D):c.1422-9dup	SEC24D	Duplication (intron variant)	Cole-Carpenter syndrome 2 +1 more	GBenign
Select item 445346	NM_014822.4(SEC24D):c.1042-6C>G	SEC24D	Single nucleotide variant (intron variant)	Cole-Carpenter syndrome 2 +1 more	GBenign/Likely benign

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