TCF3[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58787	GRCh38/hg38 19p13.3(chr19:233565-4699472)x3	ABCA7, ABHD17A +687 more	Copy number gain	See cases	GPathogenic
Select item 154560	GRCh38/hg38 19p13.3(chr19:259395-6795611)x3	ABCA7, ABHD17A +903 more	Copy number gain	See cases	GPathogenic
Select item 146110	GRCh38/hg38 19p13.3(chr19:259395-2068507)x3	STK11, TCF3 +332 more	Copy number gain	See cases	GPathogenic
Select item 59078	GRCh38/hg38 19p13.3(chr19:259395-1952650)x3	LOC130062964, LOC130062965 +321 more	Copy number gain	See cases	GPathogenic
Select item 57357	GRCh38/hg38 19p13.3(chr19:259395-2555149)x3	ABCA7, ABHD17A +429 more	Copy number gain	See cases	GPathogenic
Select item 152851	GRCh38/hg38 19p13.3(chr19:275925-1892276)x3	LOC130062905, LOC130062906 +301 more	Copy number gain	See cases	GPathogenic
Select item 145542	GRCh38/hg38 19p13.3(chr19:421537-2897921)x3	ABCA7, ABHD17A +453 more	Copy number gain	See cases	GLikely pathogenic
Select item 60066	GRCh38/hg38 19p13.3(chr19:945098-1972299)x1	LOC130062906, LOC130062907 +222 more	Copy number loss	See cases	GPathogenic
Select item 147726	GRCh38/hg38 19p13.3(chr19:1351163-2555149)x3	ABHD17A, ADAMTSL5 +219 more	Copy number gain	See cases	GUncertain significance
Select item 145414	GRCh38/hg38 19p13.3(chr19:1549144-4288720)x1	ABHD17A, ADAT3 +387 more	Copy number loss	See cases	GPathogenic
Select item 59081	GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3	ABHD17A, ADAT3 +362 more	Copy number gain	See cases	GPathogenic
Select item 3032459	NM_001136139.4(TCF3):c.*3+1G>A	TCF3	Single nucleotide variant (3 prime UTR variant +1 more)	TCF3-related condition	GLikely benign
Select item 1423705	NM_003200.5(TCF3):c.1962G>A (p.Met654Ile)	TCF3 (M653I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2081063	NM_003200.5(TCF3):c.1960A>C (p.Met654Leu)	TCF3 (M653L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1929871	NM_003200.5(TCF3):c.1958A>C (p.His653Pro)	TCF3 (H650P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1960710	NM_003200.5(TCF3):c.1956G>A (p.Gly652=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1465289	NM_003200.5(TCF3):c.1954G>A (p.Gly652Arg)	TCF3 (G649R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2419795	NM_003200.5(TCF3):c.1953C>T (p.Ala651=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1380203	NM_003200.5(TCF3):c.1951G>A (p.Ala651Thr)	TCF3 (A650T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1595129	NM_003200.5(TCF3):c.1950C>T (p.Pro650=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1518917	NM_003200.5(TCF3):c.1948C>T (p.Pro650Ser)	TCF3 (P650S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 709097	NM_003200.5(TCF3):c.1948C>A (p.Pro650Thr)	TCF3 (P649T +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1045821	NM_003200.5(TCF3):c.1945A>C (p.Asn649His)	TCF3 (N646H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2132682	NM_003200.5(TCF3):c.1942C>G (p.His648Asp)	TCF3 (H645D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1598229	NM_003200.5(TCF3):c.1940C>G (p.Ala647Gly)	TCF3 (A644G +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1491945	NM_003200.5(TCF3):c.1936G>A (p.Glu646Lys)	TCF3 (E645K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2784034	NM_003200.5(TCF3):c.1935C>G (p.Ser645Arg)	TCF3 (S642R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1606126	NM_003200.5(TCF3):c.1935C>T (p.Ser645=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2070371	NM_003200.5(TCF3):c.1933A>C (p.Ser645Arg)	TCF3 (S642R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 763988	NM_003200.5(TCF3):c.1932G>C (p.Leu644=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2861816	NM_003200.5(TCF3):c.1930C>T (p.Leu644=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2776384	NM_003200.5(TCF3):c.1926A>G (p.Pro642=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2142946	NM_003200.5(TCF3):c.1926A>T (p.Pro642=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982123	NM_003200.5(TCF3):c.1925C>G (p.Pro642Arg)	TCF3 (P639R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808057	NM_003200.5(TCF3):c.1924C>G (p.Pro642Ala)	TCF3 (P641A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1923883	NM_003200.5(TCF3):c.1919C>T (p.Pro640Leu)	TCF3 (P639L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2029658	NM_003200.5(TCF3):c.1911T>G (p.Leu637=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1720237	NM_003200.5(TCF3):c.1909C>A (p.Leu637Ile)	TCF3 (L634I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2026914	NM_003200.5(TCF3):c.1907T>C (p.Val636Ala)	TCF3 (V636A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2142947	NM_003200.5(TCF3):c.1901A>G (p.Gln634Arg)	TCF3 (Q631R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2174462	NM_003200.5(TCF3):c.1898C>T (p.Pro633Leu)	TCF3 (P633L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1973964	NM_003200.5(TCF3):c.1897C>A (p.Pro633Thr)	TCF3 (P630T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1948337	NM_003200.5(TCF3):c.1893A>G (p.Gly631=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1375523	NM_003200.5(TCF3):c.1885G>A (p.Val629Met)	TCF3 (V628M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2092171	NM_003200.5(TCF3):c.1883G>A (p.Gly628Asp)	TCF3 (G627D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2806746	NM_003200.5(TCF3):c.1867G>A (p.Glu623Lys)	TCF3 (E620K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2993764	NM_003200.5(TCF3):c.1862G>T (p.Arg621Leu)	TCF3 (R620L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2060166	NM_003200.5(TCF3):c.1862G>A (p.Arg621Gln)	TCF3 (R621Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2809635	NM_003200.5(TCF3):c.1860G>A (p.Arg620=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2765243	NM_003200.5(TCF3):c.1859G>T (p.Arg620Leu)	TCF3 (R619L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1369470	NM_003200.5(TCF3):c.1858C>T (p.Arg620Trp)	TCF3 (R619W +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2804204	NM_003200.5(TCF3):c.1857A>C (p.Lys619Asn)	TCF3 (K618N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2134536	NM_003200.5(TCF3):c.1855A>T (p.Lys619Ter)	TCF3 (K619* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1918662	NM_003200.5(TCF3):c.1831C>T (p.Leu611=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1427387	NM_003200.5(TCF3):c.1825C>T (p.Arg609Trp)	TCF3 (R608W +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1925414	NM_003200.5(TCF3):c.1823-6C>T	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1169439	NM_003200.5(TCF3):c.1823-8C>T	TCF3	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2895165	NM_003200.5(TCF3):c.1823-9T>C	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1923742	NM_003200.5(TCF3):c.1823-11C>A	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1607767	NM_003200.5(TCF3):c.1823-11C>T	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1603322	NM_003200.5(TCF3):c.1823-12C>A	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2075409	NM_003200.5(TCF3):c.1823-15C>T	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858841	NM_003200.5(TCF3):c.1823-342A>G	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956264	NM_003200.5(TCF3):c.1823-346G>A	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2759821	NM_003200.5(TCF3):c.1823-346G>T	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1631120	NM_003200.5(TCF3):c.1823-346G>C	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1651878	NM_003200.5(TCF3):c.1823-347C>T	TCF3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1635648	NM_001136139.4(TCF3):c.1795C>T (p.Leu599=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	TCF3-related condition +1 more	GLikely benign
Select item 2753450	NM_001136139.4(TCF3):c.1792G>A (p.Gly598Arg)	TCF3 (G598R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1933325	NM_001136139.4(TCF3):c.1792G>C (p.Gly598Arg)	TCF3 (G598R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1924114	NM_001136139.4(TCF3):c.1788C>T (p.Ile596=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3005965	NM_001136139.4(TCF3):c.1776C>T (p.Ala592=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2101885	NM_001136139.4(TCF3):c.1776C>G (p.Ala592=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2801399	NM_001136139.4(TCF3):c.1775C>T (p.Ala592Val)	TCF3 (A592V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2833682	NM_001136139.4(TCF3):c.1772A>T (p.Gln591Leu)	TCF3 (Q591L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1540469	NM_001136139.4(TCF3):c.1771C>T (p.Gln591Ter)	TCF3 (Q591*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 1638550	NM_001136139.4(TCF3):c.1765C>T (p.Leu589=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2997836	NM_001136139.4(TCF3):c.1764C>T (p.Ile588=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1902009	NM_001136139.4(TCF3):c.1761C>T (p.Leu587=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 626182	NM_001136139.4(TCF3):c.1755G>A (p.Lys585=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	Agammaglobulinemia 8, autosomal dominant +1 more	GUncertain significance
Select item 1642128	NM_001136139.4(TCF3):c.1746G>A (p.Ala582=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1629891	NM_001136139.4(TCF3):c.1746G>T (p.Ala582=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	TCF3-related condition +1 more	GLikely benign
Select item 1918559	NM_001136139.4(TCF3):c.1745C>T (p.Ala582Val)	TCF3 (A582V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1657704	NM_001136139.4(TCF3):c.1740C>T (p.Asp580=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1659832	NM_001136139.4(TCF3):c.1737G>C (p.Ser579=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1634390	NM_001136139.4(TCF3):c.1737G>A (p.Ser579=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2005108	NM_001136139.4(TCF3):c.1736C>T (p.Ser579Leu)	TCF3 (S579L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2959543	NM_001136139.4(TCF3):c.1733A>G (p.Lys578Arg)	TCF3 (K578R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2807485	NM_001136139.4(TCF3):c.1732A>G (p.Lys578Glu)	TCF3 (K578E)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1658765	NM_001136139.4(TCF3):c.1729C>T (p.Leu577Phe)	TCF3 (L577F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1931913	NM_001136139.4(TCF3):c.1726C>T (p.His576Tyr)	TCF3 (H576Y)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1099276	NM_001136139.4(TCF3):c.1723A>C (p.Met575Leu)	TCF3 (M575L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2081406	NM_001136139.4(TCF3):c.1722G>A (p.Gln574=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2749509	NM_001136139.4(TCF3):c.1714A>G (p.Met572Val)	TCF3 (M572V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1905557	NM_001136139.4(TCF3):c.1712G>A (p.Arg571His)	TCF3 (R571H)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1674801	NM_001136139.4(TCF3):c.1711C>T (p.Arg571Cys)	TCF3 (R571C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 546824	NM_001136139.4(TCF3):c.1700G>A (p.Arg567Gln)	TCF3 (R567Q)	Single nucleotide variant (missense variant +1 more)	not provided	GConflicting classifications of pathogenicity
Select item 1921820	NM_001136139.4(TCF3):c.1699C>T (p.Arg567Trp)	TCF3 (R567W)	Single nucleotide variant (missense variant +1 more)	TCF3-related condition +1 more	GUncertain significance
Select item 1667776	NM_001136139.4(TCF3):c.1699C>A (p.Arg567=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1638528	NM_001136139.4(TCF3):c.1698C>T (p.Phe566=)	TCF3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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