"Revvity Omics, Revvity"[submitter] AND "KCNC3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2432993	NM_004977.3(KCNC3):c.2143C>T (p.Pro715Ser)	KCNC3 (P639S +1 more)	Single nucleotide variant (missense variant +1 more)	Spinocerebellar ataxia type 13	GUncertain significance
Select item 2689283	NM_004977.3(KCNC3):c.2014C>G (p.Leu672Val)	KCNC3 (L596V +1 more)	Single nucleotide variant (missense variant +1 more)	Spinocerebellar ataxia type 13	GUncertain significance
Select item 2689284	NM_004977.3(KCNC3):c.1903G>A (p.Gly635Arg)	KCNC3 (G559R +1 more)	Single nucleotide variant (missense variant)	Spinocerebellar ataxia type 13	GUncertain significance
Select item 1573340	NM_004977.3(KCNC3):c.1876G>C (p.Gly626Arg)	KCNC3 (G550R +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2432994	NM_004977.3(KCNC3):c.1627G>A (p.Gly543Ser)	KCNC3 (G467S +1 more)	Single nucleotide variant (missense variant)	Spinocerebellar ataxia type 13	GUncertain significance
Select item 2432992	NM_004977.3(KCNC3):c.98C>G (p.Pro33Arg)	KCNC3, LOC111811967 (P33R)	Single nucleotide variant (5 prime UTR variant +1 more)	Spinocerebellar ataxia type 13	GUncertain significance

ClinVar