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

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2392400	NM_002342.3(LTBR):c.35T>A (p.Leu12Gln)	LTBR (L12Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121467	NM_002342.3(LTBR):c.52G>A (p.Val18Met)	LTBR (V18M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2509205	NM_002342.3(LTBR):c.160C>G (p.Gln54Glu)	LTBR (Q54E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3292277	NM_002342.3(LTBR):c.171C>G (p.Ile57Met)	LTBR (I57M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317741	NM_002342.3(LTBR):c.181C>T (p.Arg61Cys)	LTBR (R61C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121466	NM_002342.3(LTBR):c.221G>A (p.Arg74His)	LTBR (R101H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359616	NM_002342.3(LTBR):c.373C>G (p.Arg125Gly)	LTBR (R120G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267766	NM_002342.3(LTBR):c.566C>G (p.Thr189Ser)	LTBR (T209S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464091	NM_002342.3(LTBR):c.625A>G (p.Thr209Ala)	LTBR (T188A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3292278	NM_002342.3(LTBR):c.688G>A (p.Val230Ile)	LTBR (V211I +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3121468	NM_002342.3(LTBR):c.793C>T (p.Arg265Cys)	LTBR (R244C +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2215835	NM_002342.3(LTBR):c.794G>A (p.Arg265His)	LTBR (R244H +8 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2527110	NM_002342.3(LTBR):c.853C>A (p.Pro285Thr)	LTBR (P249T +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2527112	NM_002342.3(LTBR):c.854C>A (p.Pro285Gln)	LTBR (P249Q +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2374296	NM_002342.3(LTBR):c.913T>C (p.Ser305Pro)	LTBR (S269P +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244230	NM_002342.3(LTBR):c.922C>G (p.Leu308Val)	LTBR (L287V +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517509	NM_002342.3(LTBR):c.937G>A (p.Val313Ile)	LTBR (V313I +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3292276	NM_002342.3(LTBR):c.959A>G (p.Gln320Arg)	LTBR (Q284R +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2307933	NM_002342.3(LTBR):c.971C>T (p.Pro324Leu)	LTBR (P338L +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219401	NM_002342.3(LTBR):c.1117C>T (p.Pro373Ser)	LTBR (P337S +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401893	NM_002342.3(LTBR):c.1118C>T (p.Pro373Leu)	LTBR (P352L +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461929	NM_002342.3(LTBR):c.1181C>T (p.Pro394Leu)	LTBR (P358L +10 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2508618	NM_002342.3(LTBR):c.1294A>G (p.Ile432Val)	LTBR (I347V +10 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign

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Items: 23