IFNA5[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2620139	NM_002169.3(IFNA5):c.514A>C (p.Met172Leu)	IFNA5 (M172L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478406	NM_002169.3(IFNA5):c.481C>A (p.Pro161Thr)	IFNA5 (P161T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285360	NM_002169.3(IFNA5):c.474A>C (p.Lys158Asn)	IFNA5 (K158N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509832	NM_002169.3(IFNA5):c.446G>A (p.Arg149Lys)	IFNA5 (R149K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108266	NM_002169.3(IFNA5):c.352G>A (p.Asp118Asn)	IFNA5 (D118N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108265	NM_002169.3(IFNA5):c.346C>A (p.Leu116Met)	IFNA5 (L116M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715409	NM_002169.3(IFNA5):c.343C>T (p.Gln115Ter)	IFNA5 (Q115*)	Single nucleotide variant (nonsense)	not provided	GBenign
Select item 2211779	NM_002169.3(IFNA5):c.308C>T (p.Thr103Ile)	IFNA5 (T103I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108264	NM_002169.3(IFNA5):c.281A>G (p.Lys94Arg)	IFNA5 (K94R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208803	NM_002169.3(IFNA5):c.236T>C (p.Val79Ala)	IFNA5 (V79A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776415	NM_002169.3(IFNA5):c.197T>C (p.Phe66Ser)	IFNA5 (F66S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3108263	NM_002169.3(IFNA5):c.185C>T (p.Pro62Leu)	IFNA5 (P62L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2468487	NM_002169.3(IFNA5):c.163G>A (p.Asp55Asn)	IFNA5 (D55N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3108262	NM_002169.3(IFNA5):c.141C>G (p.Ile47Met)	IFNA5 (I47M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224532	NM_002169.3(IFNA5):c.83A>G (p.Gln28Arg)	IFNA5 (Q28R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance