MARCH6 unknown - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545014	NM_005885.4(MARCHF6):c.394G>A (p.Asp132Asn)	MARCHF6 (D27N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614624	NM_005885.4(MARCHF6):c.428G>C (p.Cys143Ser)	MARCHF6 (C143S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602772	NM_005885.4(MARCHF6):c.1087C>T (p.Arg363Cys)	MARCHF6, MIR10397 (R363C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2521606	NM_005885.4(MARCHF6):c.1676C>T (p.Thr559Ile)	MARCHF6 (T454I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477692	NM_005885.4(MARCHF6):c.2141C>T (p.Ser714Phe)	MARCHF6 (S666F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554204	NM_005885.4(MARCHF6):c.2168T>C (p.Val723Ala)	MARCHF6 (V675A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471655	NM_005885.4(MARCHF6):c.2500T>G (p.Leu834Val)	MARCHF6 (L834V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1049047	NM_005885.4(MARCHF6):c.2516C>T (p.Ala839Val)	MARCHF6 (A734V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar