Related gene-specific medical variations for Gene (Select 7469) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2296133	NM_005663.5(NELFA):c.653C>T (p.Pro218Leu)	MIR943, NELFA (P218L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 745322	NM_005663.5(NELFA):c.648C>T (p.Gly216=)	MIR943, NELFA	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 718995	NM_005663.5(NELFA):c.645A>G (p.Lys215=)	MIR943, NELFA	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

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