Related gene-specific medical variations for Gene (Select 387338) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2544160	NM_199044.4(NSUN4):c.50A>G (p.Asp17Gly)	LOC129930480, NSUN4 (D17G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284594	NM_199044.4(NSUN4):c.44G>A (p.Arg15His)	LOC129930480, NSUN4 (R15H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance