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

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3317251	NM_005410.4(SELENOP):c.1103G>C (p.Arg368Pro)	CCDC152, SELENOP (R368P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3159606	NM_005410.4(SELENOP):c.1103G>A (p.Arg368His)	CCDC152, SELENOP (R398H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3159605	NM_005410.4(SELENOP):c.1081A>G (p.Thr361Ala)	CCDC152, SELENOP (T361A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3159604	NM_005410.4(SELENOP):c.1060A>C (p.Ile354Leu)	CCDC152, SELENOP (I354L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3159615	NM_005410.4(SELENOP):c.890C>G (p.Pro297Arg)	CCDC152, SELENOP (P327R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3159614	NM_005410.4(SELENOP):c.884T>C (p.Leu295Ser)	CCDC152, SELENOP (L325S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3159613	NM_005410.4(SELENOP):c.607C>T (p.Pro203Ser)	CCDC152, SELENOP (P203S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2527084	NM_005410.4(SELENOP):c.605C>T (p.Ser202Leu)	CCDC152, SELENOP (S202L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2511083	NM_005410.4(SELENOP):c.562C>T (p.Arg188Cys)	CCDC152, SELENOP (R218C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2553607	NM_005410.4(SELENOP):c.515G>A (p.Cys172Tyr)	SELENOP (C172Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159612	NM_005410.4(SELENOP):c.431T>C (p.Val144Ala)	SELENOP (V144A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159611	NM_005410.4(SELENOP):c.382A>C (p.Asn128His)	SELENOP (N128H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159610	NM_005410.4(SELENOP):c.368T>C (p.Val123Ala)	SELENOP (V153A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526256	NM_005410.4(SELENOP):c.304C>G (p.His102Asp)	SELENOP (H102D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159608	NM_005410.4(SELENOP):c.290G>A (p.Arg97Gln)	SELENOP (R97Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3159607	NM_005410.4(SELENOP):c.220G>A (p.Val74Ile)	SELENOP (V74I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317250	NM_005410.4(SELENOP):c.112G>C (p.Asp38His)	SELENOP (D38H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569209	NM_005410.4(SELENOP):c.47C>T (p.Ser16Leu)	SELENOP (S46L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance