MT1M[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531039	NM_176870.3(MT1M):c.49G>A (p.Gly17Ser)	MT1M (G17S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2369223	NM_176870.3(MT1M):c.104C>T (p.Ser35Phe)	MT1M (S35F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379179	NM_176870.3(MT1M):c.158C>T (p.Thr53Met)	MT1M (T53M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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