"Ambry Genetics"[submitter] AND "CCDC25"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2461622	NM_018246.3(CCDC25):c.605A>G (p.Asn202Ser)	CCDC25 (N134S +2 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2377020	NM_018246.3(CCDC25):c.424C>T (p.Pro142Ser)	CCDC25 (P74S +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2384418	NM_018246.3(CCDC25):c.419G>A (p.Arg140Gln)	CCDC25 (R72Q +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2330031	NM_018246.3(CCDC25):c.326T>C (p.Ile109Thr)	CCDC25 (I109T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2308859	NM_018246.3(CCDC25):c.281C>T (p.Pro94Leu)	CCDC25 (P94L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2378201	NM_018246.3(CCDC25):c.260A>G (p.Asn87Ser)	CCDC25 (N19S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2328244	NM_018246.3(CCDC25):c.102G>T (p.Trp34Cys)	CCDC25 (W34C)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance

ClinVar