ARL6IP6[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129588	NM_152522.7(ARL6IP6):c.5C>T (p.Ser2Leu)	ARL6IP6 (S2L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129590	NM_152522.7(ARL6IP6):c.89C>T (p.Ser30Phe)	ARL6IP6 (S30F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129580	NM_152522.7(ARL6IP6):c.136G>A (p.Glu46Lys)	ARL6IP6 (E46K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481364	NM_152522.7(ARL6IP6):c.163C>G (p.Leu55Val)	ARL6IP6 (L55V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129581	NM_152522.7(ARL6IP6):c.164T>G (p.Leu55Arg)	ARL6IP6 (L55R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384961	NM_152522.7(ARL6IP6):c.166C>G (p.Arg56Gly)	ARL6IP6 (R56G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784457	NM_152522.7(ARL6IP6):c.167G>T (p.Arg56Leu)	ARL6IP6 (R56L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 372265	NM_152522.7(ARL6IP6):c.192G>A (p.Trp64Ter)	ARL6IP6 (W64*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2344051	NM_152522.7(ARL6IP6):c.200C>T (p.Pro67Leu)	ARL6IP6 (P67L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129582	NM_152522.7(ARL6IP6):c.263A>C (p.Asn88Thr)	ARL6IP6 (N88T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466087	NM_152522.7(ARL6IP6):c.277G>T (p.Ala93Ser)	ARL6IP6 (A93S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129585	NM_152522.7(ARL6IP6):c.296C>T (p.Ala99Val)	ARL6IP6 (A99V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558969	NM_152522.7(ARL6IP6):c.300G>C (p.Gln100His)	ARL6IP6 (Q100H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 775761	NM_152522.7(ARL6IP6):c.401-8A>G	ARL6IP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2206968	NM_152522.7(ARL6IP6):c.536C>T (p.Ser179Phe)	ARL6IP6 (S83F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2495878	NM_152522.7(ARL6IP6):c.574C>T (p.Pro192Ser)	ARL6IP6 (P96S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129587	NM_152522.7(ARL6IP6):c.577G>A (p.Ala193Thr)	ARL6IP6 (A162T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528991	NM_152522.7(ARL6IP6):c.605C>G (p.Ser202Cys)	ARL6IP6 (S106C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129589	NM_152522.7(ARL6IP6):c.620A>G (p.Tyr207Cys)	ARL6IP6 (Y207C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance