ClinVar (all) for Orgtrack (Select 500296) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 30638	NM_145068.4(TRPV3):c.2074T>G (p.Trp692Gly)	TRPV3 (W692G)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 30637	NM_145068.4(TRPV3):c.1717G>T (p.Gly573Cys)	TRPV3 (G573C)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 30636	NM_145068.4(TRPV3):c.1717G>A (p.Gly573Ser)	TRPV3 (G573S)	Single nucleotide variant (missense variant)	not provided	GPathogenic

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