CCDC198[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139050	NM_018168.4(CCDC198):c.799G>A (p.Glu267Lys)	CCDC198 (E267K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139049	NM_018168.4(CCDC198):c.739C>T (p.Leu247Phe)	CCDC198 (L287F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139048	NM_018168.4(CCDC198):c.719T>C (p.Ile240Thr)	CCDC198 (I239T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139047	NM_018168.4(CCDC198):c.681G>C (p.Leu227Phe)	CCDC198 (L226F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139046	NM_018168.4(CCDC198):c.564T>A (p.His188Gln)	CCDC198 (H187Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 252719	NM_018168.4(CCDC198):c.547C>T (p.Gln183Ter)	CCDC198 (Q183* +3 more)	Single nucleotide variant (nonsense)	not specified +1 more	GBenign

ClinVar