"Ambry Genetics"[submitter] AND "CD19"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2175598	NM_001770.6(CD19):c.13C>T (p.Arg5Cys)	CD19 (R5C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1954715	NM_001770.6(CD19):c.14G>A (p.Arg5His)	CD19 (R5H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2482905	NM_001770.6(CD19):c.130G>T (p.Asp44Tyr)	CD19 (D44Y)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3140367	NM_001770.6(CD19):c.140C>T (p.Thr47Ile)	CD19 (T47I)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2212201	NM_001770.6(CD19):c.194G>A (p.Ser65Asn)	CD19 (S65N)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2549340	NM_001770.6(CD19):c.239T>C (p.Ile80Thr)	CD19 (I80T)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3140370	NM_001770.6(CD19):c.495G>T (p.Glu165Asp)	CD19 (E165D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1466974	NM_001770.6(CD19):c.515C>T (p.Pro172Leu)	CD19 (P83L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 318804	NM_001770.6(CD19):c.527C>T (p.Pro176Leu)	CD19 (P176L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 3140371	NM_001770.6(CD19):c.631C>T (p.Pro211Ser)	CD19 (P211S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1520332	NM_001770.6(CD19):c.700C>T (p.Arg234Cys)	CD19 (R145C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1955092	NM_001770.6(CD19):c.830G>A (p.Arg277Gln)	CD19 (R188Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2302228	NM_001770.6(CD19):c.908G>T (p.Cys303Phe)	CD19 (C214F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1448799	NM_001770.6(CD19):c.953T>C (p.Val318Ala)	CD19 (V318A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 618002	NM_001770.6(CD19):c.962G>A (p.Arg321Lys)	CD19 (R321K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2387877	NM_001770.6(CD19):c.964A>C (p.Lys322Gln)	CD19 (K233Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207124	NM_001770.6(CD19):c.1081C>T (p.Leu361Phe)	CD19 (L361F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2394633	NM_001770.6(CD19):c.1118G>A (p.Gly373Asp)	CD19 (G284D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2613521	NM_001770.6(CD19):c.1147A>C (p.Ser383Arg)	CD19 (S294R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2518097	NM_001770.6(CD19):c.1150G>A (p.Asp384Asn)	CD19 (D295N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1448752	NM_001770.6(CD19):c.1160C>A (p.Ala387Glu)	CD19 (A298E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 318807	NM_001770.6(CD19):c.1204G>A (p.Glu402Lys)	CD19 (E402K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 2537218	NM_001770.6(CD19):c.1267A>T (p.Asn423Tyr)	CD19 (N334Y +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2547580	NM_001770.6(CD19):c.1282G>A (p.Gly428Arg)	CD19 (G339R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2541187	NM_001770.6(CD19):c.1382A>T (p.Tyr461Phe)	CD19 (Y372F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1395160	NM_001770.6(CD19):c.1417G>A (p.Ala473Thr)	CD19 (A384T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 871886	NM_001770.6(CD19):c.1612G>A (p.Asp538Asn)	CD19 (D538N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3140369	NM_001770.6(CD19):c.1637G>A (p.Gly546Glu)	CD19 (G457E +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1053341	NM_001770.6(CD19):c.1646G>A (p.Arg549His)	CD19 (R460H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2236223	NM_001770.6(CD19):c.1664C>T (p.Thr555Ile)	CD19 (T555I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 30