IFNA14[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2403784	NM_002172.3(IFNA14):c.497T>C (p.Val166Ala)	IFNA14 (V166A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108239	NM_002172.3(IFNA14):c.491G>C (p.Trp164Ser)	IFNA14 (W164S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2428778	NM_002172.3(IFNA14):c.489del (p.Trp164fs)	IFNA14 (W164fs)	Deletion (frameshift variant)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 788673	NM_002172.3(IFNA14):c.488C>T (p.Ala163Val)	IFNA14 (A163V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3108238	NM_002172.3(IFNA14):c.441C>G (p.Phe147Leu)	IFNA14 (F147L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277307	NM_002172.3(IFNA14):c.441C>A (p.Phe147Leu)	IFNA14 (F147L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342300	NM_002172.3(IFNA14):c.425C>A (p.Ala142Asp)	IFNA14 (A142D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554070	NM_002172.3(IFNA14):c.398C>T (p.Pro133Leu)	IFNA14 (P133L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588797	NM_002172.3(IFNA14):c.323T>C (p.Phe108Ser)	IFNA14 (F108S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108237	NM_002172.3(IFNA14):c.318A>C (p.Glu106Asp)	IFNA14 (E106D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2518644	NM_002172.3(IFNA14):c.295G>C (p.Ala99Pro)	IFNA14 (A99P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108236	NM_002172.3(IFNA14):c.293C>T (p.Ala98Val)	IFNA14 (A98V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108235	NM_002172.3(IFNA14):c.260C>G (p.Thr87Ser)	IFNA14 (T87S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108233	NM_002172.3(IFNA14):c.260C>A (p.Thr87Asn)	IFNA14 (T87N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344344	NM_002172.3(IFNA14):c.252G>C (p.Met84Ile)	IFNA14 (M84I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2362013	NM_002172.3(IFNA14):c.215A>G (p.Gln72Arg)	IFNA14 (Q72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108232	NM_002172.3(IFNA14):c.116T>G (p.Met39Arg)	IFNA14 (M39R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390984	NM_002172.3(IFNA14):c.22A>G (p.Met8Val)	IFNA14 (M8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance