ARL14EPL[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351308	NM_001195581.2(ARL14EPL):c.16G>A (p.Glu6Lys)	ARL14EPL (E6K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2465856	NM_001195581.2(ARL14EPL):c.32T>C (p.Ile11Thr)	ARL14EPL (I11T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2532084	NM_001195581.2(ARL14EPL):c.40A>G (p.Arg14Gly)	ARL14EPL (R14G)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2376350	NM_001195581.2(ARL14EPL):c.106G>C (p.Glu36Gln)	ARL14EPL (E36Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518810	NM_001195581.2(ARL14EPL):c.107A>G (p.Glu36Gly)	ARL14EPL (E36G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277795	NM_001195581.2(ARL14EPL):c.192A>T (p.Lys64Asn)	ARL14EPL (K64N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237362	NM_001195581.2(ARL14EPL):c.209T>C (p.Met70Thr)	ARL14EPL (M4T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606470	NM_001195581.2(ARL14EPL):c.212A>G (p.Asn71Ser)	ARL14EPL (N71S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595818	NM_001195581.2(ARL14EPL):c.237A>G (p.Lys79=)	ARL14EPL	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3129537	NM_001195581.2(ARL14EPL):c.256A>G (p.Lys86Glu)	ARL14EPL (K86E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473694	NM_001195581.2(ARL14EPL):c.295G>A (p.Asp99Asn)	ARL14EPL (D33N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309240	NM_001195581.2(ARL14EPL):c.353A>G (p.Asn118Ser)	ARL14EPL (N118S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313963	NM_001195581.2(ARL14EPL):c.354C>A (p.Asn118Lys)	ARL14EPL (N118K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236689	NM_001195581.2(ARL14EPL):c.369G>C (p.Glu123Asp)	ARL14EPL (E57D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465857	NM_001195581.2(ARL14EPL):c.383G>A (p.Arg128Gln)	ARL14EPL (R128Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129539	NM_001195581.2(ARL14EPL):c.434C>T (p.Thr145Met)	ARL14EPL (T145M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258604	NM_001195581.2(ARL14EPL):c.440C>T (p.Pro147Leu)	ARL14EPL (P147L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance