"Ambry Genetics"[submitter] AND "UBXN2B"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2600406	NM_001077619.2(UBXN2B):c.17G>C (p.Gly6Ala)	LOC130000441, UBXN2B (G6A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528192	NM_001077619.2(UBXN2B):c.17G>T (p.Gly6Val)	LOC130000441, UBXN2B (G6V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382750	NM_001077619.2(UBXN2B):c.24G>T (p.Glu8Asp)	LOC130000441, UBXN2B (E8D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3330743	NM_001077619.2(UBXN2B):c.41G>C (p.Arg14Thr)	UBXN2B (R14T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387897	NM_001077619.2(UBXN2B):c.74G>A (p.Arg25Gln)	LOC130000442, UBXN2B (R25Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185916	NM_001077619.2(UBXN2B):c.111T>A (p.Asp37Glu)	UBXN2B (D37E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185917	NM_001077619.2(UBXN2B):c.172C>T (p.Arg58Trp)	UBXN2B (R58W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273114	NM_001077619.2(UBXN2B):c.184C>G (p.Gln62Glu)	UBXN2B (Q62E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395867	NM_001077619.2(UBXN2B):c.187C>T (p.Arg63Trp)	UBXN2B (R63W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222021	NM_001077619.2(UBXN2B):c.341C>T (p.Ser114Leu)	UBXN2B (S114L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542643	NM_001077619.2(UBXN2B):c.435G>T (p.Leu145Phe)	UBXN2B (L145F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330741	NM_001077619.2(UBXN2B):c.488A>G (p.Tyr163Cys)	UBXN2B (Y163C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461045	NM_001077619.2(UBXN2B):c.646A>G (p.Ser216Gly)	UBXN2B (S216G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2205760	NM_001077619.2(UBXN2B):c.724T>A (p.Ser242Thr)	UBXN2B (S242T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2567599	NM_001077619.2(UBXN2B):c.727A>G (p.Ile243Val)	UBXN2B (I197V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318792	NM_001077619.2(UBXN2B):c.731T>C (p.Leu244Pro)	UBXN2B (L244P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513850	NM_001077619.2(UBXN2B):c.801T>A (p.Ser267Arg)	UBXN2B (S267R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249479	NM_001077619.2(UBXN2B):c.901G>T (p.Val301Leu)	UBXN2B (V255L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330742	NM_001077619.2(UBXN2B):c.962T>C (p.Ile321Thr)	UBXN2B (I275T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance