"Ambry Genetics"[submitter] AND "AIF1L"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2473920	NM_031426.4(AIF1L):c.5C>T (p.Ser2Leu)	AIF1L (S2L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102513	NM_031426.4(AIF1L):c.19A>G (p.Asn7Asp)	AIF1L (N7D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557911	NM_031426.4(AIF1L):c.91C>T (p.Arg31Trp)	AIF1L (R31W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339226	NM_031426.4(AIF1L):c.94-5405G>A	AIF1L (C33Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376491	NM_031426.4(AIF1L):c.173A>T (p.Glu58Val)	AIF1L (E84V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102523	NM_031426.4(AIF1L):c.317G>A (p.Arg106Gln)	AIF1L (R106Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2385931	NM_031426.4(AIF1L):c.419C>T (p.Pro140Leu)	AIF1L (P166L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar