Related gene-specific medical variations for Gene (Select 80117) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315008	NM_025047.3(ARL14):c.445C>G (p.Arg149Gly)	ARL14, LOC126806865 (R149G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129533	NM_025047.3(ARL14):c.8C>T (p.Ser3Leu)	ARL14, LOC126806865 (S3L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3129532	NM_025047.3(ARL14):c.53T>G (p.Leu18Arg)	ARL14, LOC126806865 (L18R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129531	NM_025047.3(ARL14):c.445C>T (p.Arg149Trp)	ARL14, LOC126806865 (R149W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129530	NM_025047.3(ARL14):c.168G>C (p.Arg56Ser)	ARL14, LOC126806865 (R56S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129529	NM_025047.3(ARL14):c.157G>A (p.Glu53Lys)	ARL14, LOC126806865 (E53K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622830	NM_025047.3(ARL14):c.433C>A (p.Leu145Ile)	ARL14, LOC126806865 (L145I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610335	NM_025047.3(ARL14):c.337A>G (p.Ile113Val)	ARL14, LOC126806865 (I113V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557781	NM_025047.3(ARL14):c.500G>T (p.Gly167Val)	ARL14, LOC126806865 (G167V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526891	NM_025047.3(ARL14):c.410C>G (p.Thr137Ser)	ARL14, LOC126806865 (T137S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515695	NM_025047.3(ARL14):c.131C>T (p.Thr44Ile)	ARL14, LOC126806865 (T44I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391427	NM_025047.3(ARL14):c.484G>A (p.Glu162Lys)	ARL14, LOC126806865 (E162K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376521	NM_025047.3(ARL14):c.395C>T (p.Thr132Ile)	ARL14, LOC126806865 (T132I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337545	NM_025047.3(ARL14):c.141C>A (p.Phe47Leu)	ARL14, LOC126806865 (F47L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293110	NM_025047.3(ARL14):c.482G>A (p.Gly161Glu)	ARL14, LOC126806865 (G161E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267128	NM_025047.3(ARL14):c.125T>A (p.Ile42Asn)	ARL14, LOC126806865 (I42N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220319	NM_025047.3(ARL14):c.382C>T (p.Pro128Ser)	ARL14, LOC126806865 (P128S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance