CD19[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 318795	NM_001770.6(CD19):c.-16G>A	CD19	Single nucleotide variant (5 prime UTR variant +1 more)	Immunodeficiency, common variable, 3	GUncertain significance
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)	not provided +1 more	GUncertain significance
Select item 318796	NM_001770.6(CD19):c.17T>G (p.Leu6Arg)	CD19 (L6R)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 3	GUncertain significance
Select item 2439814	NM_001770.6(CD19):c.24C>A (p.Phe8Leu)	CD19 (F8L)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 3	GUncertain significance
Select item 2048504	NM_001770.6(CD19):c.30C>T (p.Leu10=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1494140	NM_001770.6(CD19):c.31C>T (p.Leu11Phe)	CD19 (L11F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 799856	NM_001770.6(CD19):c.42C>T (p.Thr14=)	CD19	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 973629	NM_001770.6(CD19):c.47T>C (p.Met16Thr)	CD19 (M16T)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 3	GLikely benign
Select item 1906813	NM_001770.6(CD19):c.60C>T (p.Pro20=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 885125	NM_001770.6(CD19):c.61G>C (p.Glu21Gln)	CD19 (E21Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2966852	NM_001770.6(CD19):c.69T>G (p.Pro23=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3012595	NM_001770.6(CD19):c.88+14G>A	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1404796	NM_001770.6(CD19):c.89-12_89-3dup	CD19	Duplication (intron variant)	not provided	GLikely benign
Select item 1899929	NM_001770.6(CD19):c.94G>A (p.Asp32Asn)	CD19 (D32N)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1624512	NM_001770.6(CD19):c.99C>T (p.Asn33=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1936780	NM_001770.6(CD19):c.103G>A (p.Val35Met)	CD19 (V35M)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1582199	NM_001770.6(CD19):c.108G>A (p.Leu36=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2182006	NM_001770.6(CD19):c.119A>G (p.Lys40Arg)	CD19 (K40R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1401146	NM_001770.6(CD19):c.128C>A (p.Ser43Ter)	CD19 (S43*)	Single nucleotide variant (nonsense +2 more)	not provided	GPathogenic
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 1943026	NM_001770.6(CD19):c.140C>A (p.Thr47Asn)	CD19 (T47N)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 723603	NM_001770.6(CD19):c.147G>A (p.Gln49=)	CD19	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 254195	NM_001770.6(CD19):c.156G>C (p.Trp52Cys)	CD19 (W52C)	Single nucleotide variant (missense variant +2 more)	Immunodeficiency, common variable, 3	GPathogenic
Select item 1982326	NM_001770.6(CD19):c.160C>T (p.Arg54Trp)	CD19 (R54W)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1632954	NM_001770.6(CD19):c.165G>A (p.Glu55=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3020873	NM_001770.6(CD19):c.168C>T (p.Ser56=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1013096	NM_001770.6(CD19):c.170C>T (p.Pro57Leu)	CD19 (P57L)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 318797	NM_001770.6(CD19):c.171G>A (p.Pro57=)	CD19	Single nucleotide variant (synonymous variant +2 more)	Immunodeficiency, common variable, 3 +1 more	GConflicting classifications of pathogenicity
Select item 827973	NM_001770.6(CD19):c.178C>T (p.Pro60Ser)	CD19 (P60S)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 3 +1 more	GUncertain significance
Select item 2041811	NM_001770.6(CD19):c.179C>G (p.Pro60Arg)	CD19 (P60R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2001502	NM_001770.6(CD19):c.190C>T (p.Leu64Phe)	CD19 (L64F)	Single nucleotide variant (missense variant +2 more)	not provided	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 1955202	NM_001770.6(CD19):c.209G>A (p.Gly70Asp)	CD19 (G70D)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1033867	NM_001770.6(CD19):c.228G>T (p.Arg76Ser)	CD19 (R76S)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2972805	NM_001770.6(CD19):c.231C>A (p.Pro77=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1020999	NM_001770.6(CD19):c.233T>C (p.Leu78Pro)	CD19 (L78P)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2646356	NM_001770.6(CD19):c.237C>T (p.Ala79=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
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 886036	NM_001770.6(CD19):c.246T>C (p.Leu82=)	CD19	Single nucleotide variant (synonymous variant)	Immunodeficiency, common variable, 3	GUncertain significance
Select item 721238	NM_001770.6(CD19):c.258C>T (p.Asn86=)	CD19	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1928657	NM_001770.6(CD19):c.264T>G (p.Ser88=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1927283	NM_001770.6(CD19):c.278dup (p.Phe94fs)	CD19 (F94fs)	Duplication (frameshift variant +2 more)	not provided	GPathogenic
Select item 827692	NM_001770.6(CD19):c.274G>T (p.Gly92Trp)	CD19 (G92W)	Single nucleotide variant (missense variant)	Inherited Immunodeficiency Diseases	GLikely pathogenic
Select item 1945723	NM_001770.6(CD19):c.286C>A (p.Leu96Met)	CD19 (L96M)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1128108	NM_001770.6(CD19):c.286C>T (p.Leu96=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2770676	NM_001770.6(CD19):c.294G>A (p.Gln98=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1391946	NM_001770.6(CD19):c.297G>A (p.Pro99=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1592140	NM_001770.6(CD19):c.305C>G (p.Pro102Arg)	CD19 (P102R)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 1627365	NM_001770.6(CD19):c.306C>T (p.Pro102=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2084348	NM_001770.6(CD19):c.316G>T (p.Ala106Ser)	CD19 (A106S)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 827693	NM_001770.6(CD19):c.321G>A (p.Trp107Ter)	CD19 (W107*)	Single nucleotide variant (nonsense)	Inherited Immunodeficiency Diseases	GLikely pathogenic
Select item 886037	NM_001770.6(CD19):c.323A>C (p.Gln108Pro)	CD19 (Q108P)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1566515	NM_001770.6(CD19):c.324G>A (p.Gln108=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1362698	NM_001770.6(CD19):c.325C>T (p.Pro109Ser)	CD19 (P109S)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2905669	NM_001770.6(CD19):c.336A>G (p.Thr112=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1345217	NM_001770.6(CD19):c.341A>G (p.Asn114Ser)	CD19 (N114S)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1409038	NM_001770.6(CD19):c.354C>T (p.Ser118=)	CD19	Single nucleotide variant (synonymous variant +2 more)	not provided	GUncertain significance
Select item 1044890	NM_001770.6(CD19):c.355G>A (p.Gly119Arg)	CD19 (G119R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1592365	NM_001770.6(CD19):c.355+9C>T	CD19	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 794133	NM_001770.6(CD19):c.355+10G>A	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1636749	NM_001770.6(CD19):c.355+14T>C	CD19	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1225447	NM_001770.6(CD19):c.356-28C>G	CD19	Single nucleotide variant (intron variant +1 more)	not provided	GBenign
Select item 2714003	NM_001770.6(CD19):c.356-16C>A	CD19	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2999097	NM_001770.6(CD19):c.356-15T>C	CD19	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1954625	NM_001770.6(CD19):c.356-13G>T	CD19	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 871885	NM_001770.6(CD19):c.367C>T (p.Arg123Trp)	CD19 (R123W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1040280	NM_001770.6(CD19):c.368G>A (p.Arg123Gln)	CD19 (R123Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 318798	NM_001770.6(CD19):c.381G>A (p.Ser127=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 318799	NM_001770.6(CD19):c.384C>T (p.Asp128=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2027577	NM_001770.6(CD19):c.385C>T (p.Leu129=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 318800	NM_001770.6(CD19):c.390T>A (p.Gly130=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 318801	NM_001770.6(CD19):c.395T>G (p.Leu132Arg)	CD19 (L132R +1 more)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 3 +1 more	GConflicting classifications of pathogenicity
Select item 318802	NM_001770.6(CD19):c.406C>T (p.Leu136=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1898486	NM_001770.6(CD19):c.417G>A (p.Arg139=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1473267	NM_001770.6(CD19):c.419C>T (p.Ser140Phe)	CD19 (S51F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2878854	NM_001770.6(CD19):c.420C>T (p.Ser140=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2106286	NM_001770.6(CD19):c.421T>A (p.Ser141Thr)	CD19 (S141T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1436677	NM_001770.6(CD19):c.439C>G (p.Pro147Ala)	CD19 (P58A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2144855	NM_001770.6(CD19):c.444C>T (p.Ser148=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2065361	NM_001770.6(CD19):c.445G>A (p.Gly149Arg)	CD19 (G60R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1648907	NM_001770.6(CD19):c.474G>A (p.Val158=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 887029	NM_001770.6(CD19):c.488G>A (p.Arg163His)	CD19 (R163H)	Single nucleotide variant (missense variant)	not provided +1 more	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)	not provided	GUncertain significance
Select item 318803	NM_001770.6(CD19):c.520C>G (p.Leu174Val)	CD19 (L174V)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1999567	NM_001770.6(CD19):c.522C>G (p.Leu174=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1538906	NM_001770.6(CD19):c.522C>T (p.Leu174=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 318804	NM_001770.6(CD19):c.527C>T (p.Pro176Leu)	CD19 (P176L +1 more)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 3 +2 more	GUncertain significance
Select item 1625808	NM_001770.6(CD19):c.528G>A (p.Pro176=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 887030	NM_001770.6(CD19):c.530G>C (p.Arg177Thr)	CD19 (R177T)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 3	GUncertain significance
Select item 2117368	NM_001770.6(CD19):c.532G>A (p.Asp178Asn)	CD19 (D89N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1911387	NM_001770.6(CD19):c.552C>G (p.Leu184=)	CD19	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1941105	NM_001770.6(CD19):c.559+11G>T	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1547767	NM_001770.6(CD19):c.559+12A>G	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2852085	NM_001770.6(CD19):c.559+20G>C	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1981959	NM_001770.6(CD19):c.560-8T>C	CD19	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 546772	NM_001770.6(CD19):c.571G>A (p.Ala191Thr)	CD19 (A191T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3033921	NM_001770.6(CD19):c.603G>A (p.Gly201=)	CD19	Single nucleotide variant (synonymous variant +1 more)	CD19-related disorder	GLikely benign

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