"Ambry Genetics"[submitter] AND "IFI27"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3108123	NM_001130080.3(IFI27):c.58G>T (p.Val20Leu)	IFI27 (V20L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411105	NM_001130080.3(IFI27):c.184G>A (p.Ala62Thr)	IFI27 (A19T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285300	NM_001130080.3(IFI27):c.211A>C (p.Met71Leu)	IFI27 (M71L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621006	NM_001130080.3(IFI27):c.236G>C (p.Gly79Ala)	IFI27 (G36A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369258	NM_001130080.3(IFI27):c.260T>C (p.Leu87Pro)	IFI27 (L87P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277587	NM_001130080.3(IFI27):c.315C>G (p.Phe105Leu)	IFI27 (F105L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285299	NM_001130080.3(IFI27):c.329T>G (p.Ile110Ser)	IFI27 (I67S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460290	NM_001130080.3(IFI27):c.330T>G (p.Ile110Met)	IFI27 (I110M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar