"Ambry Genetics"[submitter] AND "SELENOI"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2454778	NM_033505.4(SELENOI):c.62G>A (p.Ser21Asn)	SELENOI (S21N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599164	NM_033505.4(SELENOI):c.77A>G (p.Asn26Ser)	SELENOI (N26S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159511	NM_033505.4(SELENOI):c.127G>A (p.Val43Ile)	SELENOI (V43I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159512	NM_033505.4(SELENOI):c.191A>G (p.Asn64Ser)	SELENOI (N64S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159514	NM_033505.4(SELENOI):c.264G>C (p.Trp88Cys)	SELENOI (W88C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159515	NM_033505.4(SELENOI):c.445A>G (p.Thr149Ala)	SELENOI (T149A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159516	NM_033505.4(SELENOI):c.564T>G (p.Ile188Met)	SELENOI (I188M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159517	NM_033505.4(SELENOI):c.592A>C (p.Ile198Leu)	SELENOI (I198L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159518	NM_033505.4(SELENOI):c.628G>A (p.Glu210Lys)	SELENOI (E210K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522200	NM_033505.4(SELENOI):c.820A>G (p.Thr274Ala)	SELENOI (T274A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469279	NM_033505.4(SELENOI):c.946C>T (p.Arg316Trp)	SELENOI (R316W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618251	NM_033505.4(SELENOI):c.991G>A (p.Val331Ile)	SELENOI (V331I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159508	NM_033505.4(SELENOI):c.1019C>T (p.Ser340Phe)	SELENOI (S340F)	Single nucleotide variant (missense variant +1 more)	Spastic paraplegia 81, autosomal recessive +1 more	GUncertain significance
Select item 3159509	NM_033505.4(SELENOI):c.1024G>T (p.Val342Phe)	SELENOI (V342F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159510	NM_033505.4(SELENOI):c.1103A>G (p.Gln368Arg)	SELENOI (Q368R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance