MRPL36[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2243219	NM_032479.4(MRPL36):c.292C>G (p.His98Asp)	MRPL36 (H98D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3207559	NM_032479.4(MRPL36):c.223C>A (p.Arg75Ser)	MRPL36 (R75S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589451	NM_032479.4(MRPL36):c.170T>G (p.Leu57Arg)	MRPL36 (L57R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255654	NM_032479.4(MRPL36):c.146G>A (p.Arg49His)	MRPL36 (R49H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312690	NM_032479.4(MRPL36):c.76C>G (p.Leu26Val)	MRPL36 (L26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3207572	NM_032479.4(MRPL36):c.70C>G (p.Arg24Gly)	MRPL36 (R24G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376499	NM_032479.4(MRPL36):c.53G>A (p.Arg18His)	MRPL36 (R18H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar