"Ambry Genetics"[submitter] AND "SELENBP1"[gene] - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3159484	NM_003944.4(SELENBP1):c.1393G>A (p.Asp465Asn)	SELENBP1 (D465N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236433	NM_003944.4(SELENBP1):c.1388G>T (p.Gly463Val)	SELENBP1 (G401V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387385	NM_003944.4(SELENBP1):c.1337T>A (p.Phe446Tyr)	SELENBP1 (F384Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243121	NM_003944.4(SELENBP1):c.1323C>G (p.Asn441Lys)	SELENBP1 (N483K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279568	NM_003944.4(SELENBP1):c.1252A>C (p.Ile418Leu)	SELENBP1 (I418L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159483	NM_003944.4(SELENBP1):c.1208C>A (p.Thr403Lys)	SELENBP1 (T445K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620894	NM_003944.4(SELENBP1):c.1130T>C (p.Val377Ala)	SELENBP1 (V377A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355340	NM_003944.4(SELENBP1):c.1111T>C (p.Ser371Pro)	SELENBP1 (S309P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618218	NM_003944.4(SELENBP1):c.1054G>C (p.Gly352Arg)	SELENBP1 (G290R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307997	NM_003944.4(SELENBP1):c.1037C>G (p.Thr346Arg)	SELENBP1 (T284R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159482	NM_003944.4(SELENBP1):c.1028C>T (p.Pro343Leu)	SELENBP1 (P281L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317221	NM_003944.4(SELENBP1):c.1002G>C (p.Gln334His)	SELENBP1 (Q334H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542111	NM_003944.4(SELENBP1):c.981G>C (p.Trp327Cys)	SELENBP1 (W327C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236434	NM_003944.4(SELENBP1):c.970T>C (p.Phe324Leu)	SELENBP1 (F262L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231538	NM_003944.4(SELENBP1):c.968A>G (p.Tyr323Cys)	SELENBP1 (Y261C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395988	NM_003944.4(SELENBP1):c.958C>T (p.Arg320Cys)	SELENBP1 (R258C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159496	NM_003944.4(SELENBP1):c.934G>A (p.Asp312Asn)	SELENBP1 (D250N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484033	NM_003944.4(SELENBP1):c.893T>G (p.Val298Gly)	SELENBP1 (V340G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159495	NM_003944.4(SELENBP1):c.887A>G (p.Lys296Arg)	SELENBP1 (K296R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159494	NM_003944.4(SELENBP1):c.880C>T (p.Pro294Ser)	SELENBP1 (P336S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345909	NM_003944.4(SELENBP1):c.841G>A (p.Glu281Lys)	SELENBP1 (E323K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343131	NM_003944.4(SELENBP1):c.805G>A (p.Ala269Thr)	SELENBP1 (A311T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398235	NM_003944.4(SELENBP1):c.781G>A (p.Ala261Thr)	SELENBP1 (A199T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347376	NM_003944.4(SELENBP1):c.761G>A (p.Arg254His)	SELENBP1 (R192H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159493	NM_003944.4(SELENBP1):c.760C>T (p.Arg254Cys)	SELENBP1 (R296C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159492	NM_003944.4(SELENBP1):c.649G>A (p.Ala217Thr)	SELENBP1 (A259T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159491	NM_003944.4(SELENBP1):c.574T>C (p.Tyr192His)	SELENBP1 (Y234H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159490	NM_003944.4(SELENBP1):c.545G>C (p.Gly182Ala)	SELENBP1 (G120A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159489	NM_003944.4(SELENBP1):c.539C>G (p.Pro180Arg)	SELENBP1 (P180R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282310	NM_003944.4(SELENBP1):c.505G>A (p.Glu169Lys)	SELENBP1 (E107K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244988	NM_003944.4(SELENBP1):c.485G>A (p.Gly162Asp)	SELENBP1 (G162D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296016	NM_003944.4(SELENBP1):c.474T>A (p.Asn158Lys)	SELENBP1 (N158K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159488	NM_003944.4(SELENBP1):c.466A>G (p.Lys156Glu)	SELENBP1 (K156E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458810	NM_003944.4(SELENBP1):c.436G>A (p.Glu146Lys)	SELENBP1 (E188K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220737	NM_003944.4(SELENBP1):c.400G>C (p.Ala134Pro)	SELENBP1 (A134P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399587	NM_003944.4(SELENBP1):c.365T>C (p.Ile122Thr)	SELENBP1 (I122T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159486	NM_003944.4(SELENBP1):c.283G>C (p.Val95Leu)	SELENBP1 (V137L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159485	NM_003944.4(SELENBP1):c.184C>T (p.Arg62Trp)	SELENBP1 (R104W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159487	NM_003944.4(SELENBP1):c.31G>A (p.Gly11Ser)	SELENBP1 (G53S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 39