C5774249[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1722510	NM_002224.4(ITPR3):c.4271C>T (p.Thr1424Met)	ITPR3 (T1424M)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease, demyelinating, type 1J	GLikely pathogenic
Select item 2689266	NM_002224.4(ITPR3):c.5138-8G>A	ITPR3	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease, demyelinating, type 1J	GUncertain significance