"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "MED25"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 573830	NM_030973.4(MED25):c.801dup (p.Val268fs)	MED25 (V268fs)	Duplication (frameshift variant)	not provided +1 more	GUncertain significance
Select item 1693753	NM_030973.4(MED25):c.1190A>G (p.Asn397Ser)	MED25 (N397S)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease type 2 +1 more	GUncertain significance
Select item 1302976	NM_030973.4(MED25):c.1202C>T (p.Ala401Val)	MED25 (A401V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 939689	NM_030973.4(MED25):c.1308C>T (p.Gly436=)	MED25	Single nucleotide variant (synonymous variant)	not provided +1 more	GUncertain significance
Select item 958450	NM_030973.4(MED25):c.1795_1803del (p.Ser599_Ala601del)	MED25	Deletion (inframe_deletion)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1162843	NM_030973.4(MED25):c.1807G>A (p.Gly603Arg)	MED25 (G603R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar