IFI27L1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2393441	NM_206949.3(IFI27L1):c.41T>C (p.Val14Ala)	IFI27L1 (V14A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3108126	NM_206949.3(IFI27L1):c.46G>A (p.Ala16Thr)	IFI27L1 (A16T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108127	NM_206949.3(IFI27L1):c.55G>A (p.Gly19Arg)	IFI27L1 (G19R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2428766	NM_206949.3(IFI27L1):c.61+1G>A	IFI27L1	Single nucleotide variant (splice donor variant)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 3108128	NM_206949.3(IFI27L1):c.85G>A (p.Val29Met)	IFI27L1 (V29M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464728	NM_206949.3(IFI27L1):c.97G>A (p.Ala33Thr)	IFI27L1 (A33T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108124	NM_206949.3(IFI27L1):c.137T>C (p.Ile46Thr)	IFI27L1 (I46T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323024	NM_206949.3(IFI27L1):c.151A>G (p.Met51Val)	IFI27L1 (M51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348900	NM_206949.3(IFI27L1):c.178G>A (p.Gly60Ser)	IFI27L1 (G60S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108125	NM_206949.3(IFI27L1):c.202G>C (p.Val68Leu)	IFI27L1 (V68L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385167	NM_206949.3(IFI27L1):c.205G>T (p.Ala69Ser)	IFI27L1 (A69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303030	NM_206949.3(IFI27L1):c.235C>T (p.Leu79Phe)	IFI27L1 (L79F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221190	NM_206949.3(IFI27L1):c.263G>T (p.Gly88Val)	IFI27L1 (G88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance