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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3142398	NM_024053.5(CENPM):c.475G>A (p.Gly159Ser)	CENPM (G159S +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2466823	NM_024053.5(CENPM):c.445G>C (p.Val149Leu)	CENPM (V115L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2552433	NM_024053.5(CENPM):c.392G>A (p.Cys131Tyr)	CENPM (C131Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3142397	NM_024053.5(CENPM):c.340C>T (p.Arg114Trp)	CENPM (P108L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552581	NM_024053.5(CENPM):c.316C>T (p.Arg106Trp)	CENPM (R106W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3142396	NM_024053.5(CENPM):c.16C>T (p.Pro6Ser)	CENPM, LOC130067578 +1 more (P6S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

ClinVar