"Ambry Genetics"[submitter] AND "C10orf90"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2406264	NM_001350921.2(C10orf90):c.2015C>T (p.Ala672Val)	C10orf90, LOC728158 (A672V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216839	NM_001350921.2(C10orf90):c.1931G>T (p.Arg644Leu)	C10orf90 (R547L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214023	NM_001350921.2(C10orf90):c.1399A>G (p.Asn467Asp)	C10orf90 (N467D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380464	NM_001350921.2(C10orf90):c.1151G>A (p.Arg384Lys)	C10orf90 (R287K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3135658	NM_001350921.2(C10orf90):c.1052T>C (p.Leu351Pro)	C10orf90 (L254P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366240	NM_001350921.2(C10orf90):c.611T>C (p.Leu204Ser)	C10orf90 (L107S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar