"Ambry Genetics"[submitter] AND "DICER1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 315099	NM_177438.3(DICER1):c.*5G>A	DICER1	Single nucleotide variant (3 prime UTR variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 479616	NM_177438.3(DICER1):c.*4C>T	DICER1	Single nucleotide variant (3 prime UTR variant)	DICER1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1749514	NM_177438.3(DICER1):c.5768G>A (p.Ter1923=)	DICER1	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 825951	NM_177438.3(DICER1):c.5766C>G (p.Ser1922Arg)	DICER1 (S1922R)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 840696	NM_177438.3(DICER1):c.5765G>A (p.Ser1922Asn)	DICER1 (S1922N)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 479620	NM_177438.3(DICER1):c.5763T>C (p.Asn1921=)	DICER1	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 477273	NM_177438.3(DICER1):c.5762A>G (p.Asn1921Ser)	DICER1 (N1921S)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 644129	NM_177438.3(DICER1):c.5761A>C (p.Asn1921His)	DICER1 (N1921H)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1749483	NM_177438.3(DICER1):c.5760C>G (p.Pro1920=)	DICER1	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 885931	NM_177438.3(DICER1):c.5758C>T (p.Pro1920Ser)	DICER1 (P1920S)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 1447617	NM_177438.3(DICER1):c.5752C>T (p.Gln1918Ter)	DICER1 (Q1918*)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1749443	NM_177438.3(DICER1):c.5751T>C (p.Pro1917=)	DICER1	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 479646	NM_177438.3(DICER1):c.5750C>G (p.Pro1917Arg)	DICER1 (P1917R)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 242143	NM_177438.3(DICER1):c.5748A>G (p.Gln1916=)	DICER1	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related condition +2 more	GLikely benign
Select item 825934	NM_177438.3(DICER1):c.5744A>G (p.Asn1915Ser)	DICER1 (N1915S)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1749393	NM_177438.3(DICER1):c.5741C>A (p.Ala1914Asp)	DICER1 (A1779D +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1718434	NM_177438.3(DICER1):c.5741C>T (p.Ala1914Val)	DICER1 (A1353V +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2566172	NM_177438.3(DICER1):c.5740G>A (p.Ala1914Thr)	DICER1 (A1725T +4 more)	Single nucleotide variant (missense variant +2 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 1749390	NM_177438.3(DICER1):c.5740G>C (p.Ala1914Pro)	DICER1 (A1725P +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 315100	NM_177438.3(DICER1):c.5738A>G (p.Lys1913Arg)	DICER1 (K1913R)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 477270	NM_177438.3(DICER1):c.5736C>G (p.Leu1912=)	DICER1	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 1749339	NM_177438.3(DICER1):c.5732G>T (p.Ser1911Ile)	DICER1 (S1722I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1004133	NM_177438.3(DICER1):c.5731A>G (p.Ser1911Gly)	DICER1 (S1911G)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 825925	NM_177438.3(DICER1):c.5729G>A (p.Arg1910Gln)	DICER1 (R1910Q)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1025708	NM_177438.3(DICER1):c.5728C>T (p.Arg1910Ter)	DICER1 (R1910*)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 1749297	NM_177438.3(DICER1):c.5724C>G (p.Ala1908=)	DICER1	Single nucleotide variant (synonymous variant +2 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 2566206	NM_177438.3(DICER1):c.5720G>T (p.Arg1907Ile)	DICER1 (R1346I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1116905	NM_177438.3(DICER1):c.5712A>G (p.Ala1904=)	DICER1	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 477268	NM_177438.3(DICER1):c.5706T>C (p.Ser1902=)	DICER1	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 1749182	NM_177438.3(DICER1):c.5702A>T (p.Lys1901Ile)	DICER1 (K1340I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 543709	NM_177438.3(DICER1):c.5691C>T (p.Tyr1897=)	DICER1	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 935531	NM_177438.3(DICER1):c.5684G>A (p.Arg1895Gln)	DICER1 (R1895Q)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 483408	NM_177438.3(DICER1):c.5678T>C (p.Val1893Ala)	DICER1 (V1893A)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 483445	NM_177438.3(DICER1):c.5677G>A (p.Val1893Ile)	DICER1 (V1893I)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 2586387	NM_177438.3(DICER1):c.5664del (p.Lys1889fs)	DICER1 (K1795fs +4 more)	Deletion (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1748927	NM_177438.3(DICER1):c.5661G>C (p.Lys1887Asn)	DICER1 (K1887N +4 more)	Single nucleotide variant (missense variant +2 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 2586406	NM_177438.3(DICER1):c.5654T>G (p.Val1885Gly)	DICER1 (V1324G +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 417042	NM_177438.3(DICER1):c.5652A>G (p.Val1884=)	DICER1	Single nucleotide variant (stop lost +1 more)	DICER1-related tumor predisposition +1 more	GConflicting classifications of pathogenicity
Select item 2446238	NM_177438.3(DICER1):c.5646G>A (p.Val1882=)	DICER1 (W1828*)	Single nucleotide variant (synonymous variant +3 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 220945	NM_177438.3(DICER1):c.5643T>C (p.Thr1881=)	DICER1 (L1827P)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +4 more	GLikely benign
Select item 825868	NM_177438.3(DICER1):c.5641A>G (p.Thr1881Ala)	DICER1 (T1881A)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1748786	NM_177438.3(DICER1):c.5639T>G (p.Val1880Gly)	DICER1 (S1826A +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1748723	NM_177438.3(DICER1):c.5628G>A (p.Gly1876=)	DICER1 (G1822E)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1116097	NM_177438.3(DICER1):c.5628G>C (p.Gly1876=)	DICER1 (G1822A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 429154	NM_177438.3(DICER1):c.5626G>A (p.Gly1876Arg)	DICER1 (G1876R)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1748715	NM_177438.3(DICER1):c.5625C>A (p.Asp1875Glu)	DICER1 (D1314E +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 417064	NM_177438.3(DICER1):c.5625C>T (p.Asp1875=)	DICER1 (T1821M)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GLikely benign
Select item 2586420	NM_177438.3(DICER1):c.5624A>T (p.Asp1875Val)	DICER1 (D1314V +5 more)	Single nucleotide variant (missense variant +2 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 412160	NM_177438.3(DICER1):c.5623G>A (p.Asp1875Asn)	DICER1 (D1875N)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 2586390	NM_177438.3(DICER1):c.5621dup (p.Tyr1874Ter)	DICER1 (T1820fs +5 more)	Duplication (frameshift variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 933131	NM_177438.3(DICER1):c.5622C>G (p.Tyr1874Ter)	DICER1 (T1820R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 648917	NM_177438.3(DICER1):c.5622C>A (p.Tyr1874Ter)	DICER1 (Y1874* +1 more)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 417051	NM_177438.3(DICER1):c.5622C>T (p.Tyr1874=)	DICER1 (T1820M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1629827	NM_177438.3(DICER1):c.5619T>C (p.Thr1873=)	DICER1 (L1819P)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 724126	NM_177438.3(DICER1):c.5616A>G (p.Arg1872=)	DICER1 (E1818G)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 2566170	NM_177438.3(DICER1):c.5615G>A (p.Arg1872Lys)	DICER1 (R1872K +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2566157	NM_177438.3(DICER1):c.5611G>A (p.Glu1871Lys)	DICER1 (E1682K +4 more)	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 543713	NM_177438.3(DICER1):c.5607G>A (p.Pro1869=)	DICER1 (R1815Q)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 543571	NM_177438.3(DICER1):c.5606C>T (p.Pro1869Leu)	DICER1 (P1869L +1 more)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 825847	NM_177438.3(DICER1):c.5602A>T (p.Ser1868Cys)	DICER1 (S1868C +1 more)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 825844	NM_177438.3(DICER1):c.5598A>G (p.Lys1866=)	DICER1 (N1812S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1748508	NM_177438.3(DICER1):c.5595C>T (p.Ala1865=)	DICER1 (P1811L)	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2492672	NM_177438.3(DICER1):c.5591C>T (p.Thr1864Ile)	DICER1 (T1675I +4 more)	Single nucleotide variant (synonymous variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 754164	NM_177438.3(DICER1):c.5583A>G (p.Glu1861=)	DICER1 (N1807S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1748375	NM_177438.3(DICER1):c.5571G>A (p.Leu1857=)	DICER1 (C1803Y)	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1632016	NM_177438.3(DICER1):c.5569T>C (p.Leu1857=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 749630	NM_177438.3(DICER1):c.5568A>G (p.Glu1856=)	DICER1 (N1802S)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 2566204	NM_177438.3(DICER1):c.5567A>C (p.Glu1856Ala)	DICER1 (E1295A +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 651007	NM_177438.3(DICER1):c.5566G>C (p.Glu1856Gln)	DICER1 (E1856Q +1 more)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 1748331	NM_177438.3(DICER1):c.5565A>C (p.Arg1855=)	DICER1 (E1801A)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 2566230	NM_177438.3(DICER1):c.5564G>C (p.Arg1855Pro)	DICER1 (R1666P +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1748327	NM_177438.3(DICER1):c.5564G>A (p.Arg1855Gln)	DICER1 (R1294Q +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1118176	NM_177438.3(DICER1):c.5563C>A (p.Arg1855=)	DICER1 (C1800*)	Single nucleotide variant (nonsense +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 947388	NM_177438.3(DICER1):c.5563C>T (p.Arg1855Ter)	DICER1 (R1855*)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 543707	NM_177438.3(DICER1):c.5562G>A (p.Val1854=)	DICER1 (C1800Y)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 758406	NM_177438.3(DICER1):c.5556C>T (p.Ser1852=)	DICER1 (P1798L)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 417083	NM_177438.3(DICER1):c.5556C>A (p.Ser1852=)	DICER1 (P1798H)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 749880	NM_177438.3(DICER1):c.5553T>G (p.Arg1851=)	DICER1 (V1797G)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 825824	NM_177438.3(DICER1):c.5552G>A (p.Arg1851His)	DICER1 (R1851H +1 more)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 825823	NM_177438.3(DICER1):c.5551C>T (p.Arg1851Cys)	DICER1 (R1851C)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 763191	NM_177438.3(DICER1):c.5550C>G (p.Pro1850=)	DICER1 (P1796R)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 723047	NM_177438.3(DICER1):c.5550C>T (p.Pro1850=)	DICER1 (P1796L)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GLikely benign
Select item 850385	NM_177438.3(DICER1):c.5545G>A (p.Val1849Ile)	DICER1 (V1849I +1 more)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 825819	NM_177438.3(DICER1):c.5544T>C (p.Asn1848=)	DICER1 (M1794T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 825817	NM_177438.3(DICER1):c.5542A>G (p.Asn1848Asp)	DICER1 (N1848D)	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 483443	NM_177438.3(DICER1):c.5530A>G (p.Lys1844Glu)	DICER1 (K1844E)	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 477263	NM_177438.3(DICER1):c.5529A>G (p.Glu1843=)	DICER1 (K1789R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1748100	NM_177438.3(DICER1):c.5528A>G (p.Glu1843Gly)	DICER1 (E1654G +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 825805	NM_177438.3(DICER1):c.5527+4T>A	DICER1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 825804	NM_177438.3(DICER1):c.5527+3A>G	DICER1	Single nucleotide variant (intron variant)	DICER1-related tumor predisposition	GLikely pathogenic FDA Recognized database
Select item 2586389	NM_177438.3(DICER1):c.5527G>A (p.Glu1843Lys)	DICER1 (E1654K +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 242139	NM_177438.3(DICER1):c.5524A>G (p.Ile1842Val)	DICER1 (I1842V)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1748088	NM_177438.3(DICER1):c.5523A>G (p.Leu1841=)	DICER1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2566207	NM_177438.3(DICER1):c.5522T>A (p.Leu1841Gln)	DICER1 (L1706Q +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 477262	NM_177438.3(DICER1):c.5521C>T (p.Leu1841=)	DICER1	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 1748082	NM_177438.3(DICER1):c.5520A>C (p.Pro1840=)	DICER1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 242138	NM_177438.3(DICER1):c.5520A>G (p.Pro1840=)	DICER1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1748060	NM_177438.3(DICER1):c.5519C>T (p.Pro1840Leu)	DICER1 (P1705L +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1748057	NM_177438.3(DICER1):c.5517G>C (p.Arg1839=)	DICER1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1157221	NM_177438.3(DICER1):c.5517G>A (p.Arg1839=)	DICER1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign

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