Related gene-specific medical variations for Gene (Select 64757) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3213410	NM_022746.4(MTARC1):c.914G>A (p.Arg305Gln)	LOC126806018, MTARC1 (R305Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3213405	NM_022746.4(MTARC1):c.893G>A (p.Arg298His)	LOC126806018, MTARC1 (R298H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3213398	NM_022746.4(MTARC1):c.890A>G (p.Tyr297Cys)	LOC126806018, MTARC1 (Y297C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513503	NM_022746.4(MTARC1):c.892C>T (p.Arg298Cys)	LOC126806018, MTARC1 (R298C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787652	NM_022746.4(MTARC1):c.888-10C>T	LOC126806018, MTARC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 779860	NM_022746.4(MTARC1):c.357C>T (p.Cys119=)	MTARC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 773643	NM_022746.4(MTARC1):c.660G>A (p.Ser220=)	MTARC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 773642	NM_022746.4(MTARC1):c.286G>C (p.Val96Leu)	MTARC1 (V96L)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar