MT1G[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2365060	NM_001301267.2(MT1G):c.184G>A (p.Ala62Thr)	MT1G (A62T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275940	NM_001301267.2(MT1G):c.166G>A (p.Glu56Lys)	MT1G (E55K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331531	NM_001301267.2(MT1G):c.122G>C (p.Gly41Ala)	MT1G (G41A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212961	NM_001301267.2(MT1G):c.118G>A (p.Val40Met)	MT1G (V39M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486472	NM_001301267.2(MT1G):c.98G>C (p.Ser33Thr)	MT1G (S33T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386860	NM_001301267.2(MT1G):c.38C>T (p.Ser13Phe)	MT1G (S13F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212971	NM_001301267.2(MT1G):c.11A>G (p.Asn4Ser)	MT1G (N4S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar