Related gene-specific medical variations for Gene (Select 57106) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176252	NM_020378.4(NAT14):c.8C>T (p.Pro3Leu)	LOC130065122, NAT14 (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176209	NM_020378.4(NAT14):c.11G>A (p.Ser4Asn)	LOC130065122, NAT14 (S4N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276480	NM_020378.4(NAT14):c.40G>A (p.Asp14Asn)	LOC130065122, NAT14 (D14N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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