NCS1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 750286	NM_014286.4(NCS1):c.186C>A (p.Thr62=)	NCS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3298943	NM_014286.4(NCS1):c.211G>A (p.Val71Ile)	NCS1 (V53I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313248	NM_014286.4(NCS1):c.269C>T (p.Ser90Leu)	NCS1 (S72L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359595	NM_014286.4(NCS1):c.356A>G (p.Asn119Ser)	NCS1 (N119S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713334	NM_014286.4(NCS1):c.396+10C>T	NCS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3185424	NM_014286.4(NCS1):c.406G>A (p.Val136Met)	NCS1 (V136M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722066	NM_014286.4(NCS1):c.474+8G>T	NCS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2494069	NM_014286.4(NCS1):c.559G>C (p.Asp187His)	NCS1 (D169H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar