METTL11B - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2610579	NM_001136107.2(NTMT2):c.11G>A (p.Arg4Gln)	NTMT2 (R4Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602546	NM_001136107.2(NTMT2):c.323T>C (p.Phe108Ser)	NTMT2 (F108S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2592523	NM_001136107.2(NTMT2):c.482T>A (p.Val161Asp)	NTMT2 (V161D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2478268	NM_001136107.2(NTMT2):c.583C>G (p.His195Asp)	NTMT2 (H195D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495897	NM_001136107.2(NTMT2):c.608C>T (p.Ala203Val)	NTMT2 (A203V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2456726	NM_001136107.2(NTMT2):c.814G>A (p.Val272Met)	NTMT2 (V272M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469275	NM_001136107.2(NTMT2):c.826G>A (p.Ala276Thr)	NTMT2 (A276T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar