"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MYH9"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 902430	NM_002473.6(MYH9):c.5878G>A (p.Glu1960Lys)	MYH9 (E1960K)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341490	NM_002473.6(MYH9):c.5877C>T (p.Ala1959=)	MYH9	Single nucleotide variant (synonymous variant)	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss +4 more	GBenign/Likely benign
Select item 2433953	NM_002473.6(MYH9):c.5854G>C (p.Asp1952His)	MYH9 (D1952H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 504938	NM_002473.6(MYH9):c.5853G>A (p.Ala1951=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 1304481	NM_002473.6(MYH9):c.5851G>A (p.Ala1951Thr)	MYH9 (A1951T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1920685	NM_002473.6(MYH9):c.5842G>C (p.Asp1948His)	MYH9 (D1948H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1307714	NM_002473.6(MYH9):c.5833G>A (p.Glu1945Lys)	MYH9 (E1945K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 227617	NM_002473.6(MYH9):c.5832C>T (p.Asp1944=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 871550	NM_002473.6(MYH9):c.5829C>T (p.Ser1943=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 44573	NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg)	MYH9 (G1940R)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 258761	NM_002473.6(MYH9):c.5817C>T (p.Ala1939=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 178424	NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr)	MYH9 (A1939T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +4 more	GBenign/Likely benign
Select item 1215129	NM_002473.6(MYH9):c.5814C>T (p.Gly1938=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1723053	NM_002473.6(MYH9):c.5807G>A (p.Arg1936Gln)	MYH9 (R1936Q)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 164412	NM_002473.6(MYH9):c.5806C>T (p.Arg1936Trp)	MYH9 (R1936W)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +3 more	GConflicting classifications of pathogenicity
Select item 14072	NM_002473.6(MYH9):c.5797C>T (p.Arg1933Ter)	MYH9 (R1933*)	Single nucleotide variant (nonsense)	Autosomal dominant nonsyndromic hearing loss 17 +3 more	GPathogenic
Select item 1200857	NM_002473.6(MYH9):c.5788G>A (p.Val1930Met)	MYH9 (V1930M)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 903289	NM_002473.6(MYH9):c.5787C>T (p.Val1929=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2170164	NM_002473.6(MYH9):c.5781G>A (p.Pro1927=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 44572	NM_002473.6(MYH9):c.5781G>T (p.Pro1927=)	MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +4 more	GBenign
Select item 2087813	NM_002473.6(MYH9):c.5773G>A (p.Asp1925Asn)	MYH9 (D1925N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 44571	NM_002473.6(MYH9):c.5766-3del	MYH9	Deletion	Nonsyndromic Hearing Loss, Dominant +4 more	GBenign
Select item 258760	NM_002473.6(MYH9):c.5766-5C>T	MYH9	Single nucleotide variant (intron variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 1989326	NM_002473.6(MYH9):c.5765+20C>T	MYH9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1939509	NM_002473.6(MYH9):c.5765+15C>T	MYH9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 341491	NM_002473.6(MYH9):c.5765+9C>T	MYH9	Single nucleotide variant (intron variant)	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss +3 more	GBenign/Likely benign
Select item 2890483	NM_002473.6(MYH9):c.5765+8G>A	MYH9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 517574	NM_002473.6(MYH9):c.5765+8G>T	MYH9	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 258759	NM_002473.6(MYH9):c.5765+7C>T	MYH9	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2714905	NM_002473.6(MYH9):c.5765+4A>G	MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 737359	NM_002473.6(MYH9):c.5764A>C (p.Arg1922=)	MYH9	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 2415987	NM_002473.6(MYH9):c.5760G>A (p.Lys1920=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976025	NM_002473.6(MYH9):c.5748C>G (p.Ser1916=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1220156	NM_002473.6(MYH9):c.5742C>T (p.Val1914=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1945867	NM_002473.6(MYH9):c.5736C>T (p.Arg1912=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903357	NM_002473.6(MYH9):c.5722G>A (p.Asp1908Asn)	MYH9 (D1908N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1984189	NM_002473.6(MYH9):c.5721C>T (p.Ala1907=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 179209	NM_002473.6(MYH9):c.5718G>A (p.Thr1906=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 341492	NM_002473.6(MYH9):c.5717C>T (p.Thr1906Met)	MYH9 (T1906M)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GConflicting classifications of pathogenicity
Select item 3019120	NM_002473.6(MYH9):c.5711C>T (p.Thr1904Ile)	MYH9 (T1904I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 258758	NM_002473.6(MYH9):c.5709C>T (p.Ala1903=)	MYH9	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1968954	NM_002473.6(MYH9):c.5706C>G (p.Asp1902Glu)	MYH9 (D1902E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 623990	NM_002473.6(MYH9):c.5695G>A (p.Glu1899Lys)	MYH9 (E1899K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1120142	NM_002473.6(MYH9):c.5694C>T (p.Arg1898=)	MYH9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 829957	NM_002473.6(MYH9):c.5671G>A (p.Ala1891Thr)	MYH9 (A1891T)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1906573	NM_002473.6(MYH9):c.5670C>T (p.Asn1890=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2988558	NM_002473.6(MYH9):c.5661G>A (p.Gln1887=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2086779	NM_002473.6(MYH9):c.5659C>G (p.Gln1887Glu)	MYH9 (Q1887E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911702	NM_002473.6(MYH9):c.5646C>T (p.Ala1882=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2865321	NM_002473.6(MYH9):c.5644G>A (p.Ala1882Thr)	MYH9 (A1882T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2828520	NM_002473.6(MYH9):c.5643G>A (p.Glu1881=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 633676	NM_002473.6(MYH9):c.5630G>A (p.Arg1877Gln)	MYH9 (R1877Q)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1709634	NM_002473.6(MYH9):c.5629C>T (p.Arg1877Trp)	MYH9 (R1877W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 809356	NM_002473.6(MYH9):c.5610C>T (p.Thr1870=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2100602	NM_002473.6(MYH9):c.5597A>G (p.Asp1866Gly)	MYH9 (D1866G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2890324	NM_002473.6(MYH9):c.5596G>C (p.Asp1866His)	MYH9 (D1866H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3004451	NM_002473.6(MYH9):c.5595C>T (p.Ala1865=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1192912	NM_002473.6(MYH9):c.5593-4G>A	MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 341493	NM_002473.6(MYH9):c.5593-14G>A	MYH9	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GConflicting classifications of pathogenicity
Select item 164415	NM_002473.6(MYH9):c.5593-14G>T	MYH9	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign
Select item 3003250	NM_002473.6(MYH9):c.5592+9G>A	MYH9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2726143	NM_002473.6(MYH9):c.5592+7G>A	MYH9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 792938	NM_002473.6(MYH9):c.5571C>T (p.Asn1857=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2176904	NM_002473.6(MYH9):c.5559C>T (p.Asp1853=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 717105	NM_002473.6(MYH9):c.5542C>G (p.Leu1848Val)	MYH9 (L1848V)	Single nucleotide variant (missense variant)	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss +2 more	GConflicting classifications of pathogenicity
Select item 14073	NM_002473.6(MYH9):c.5521G>A (p.Glu1841Lys)	MYH9 (E1841K)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 3003422	NM_002473.6(MYH9):c.5498C>T (p.Ala1833Val)	MYH9 (A1833V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831040	NM_002473.6(MYH9):c.5484-11C>G	MYH9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1620536	NM_002473.6(MYH9):c.5483+19G>A	MYH9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1636042	NM_002473.6(MYH9):c.5483+18C>T	MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 2192084	NM_002473.6(MYH9):c.5483+5G>C	MYH9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 667132	NM_002473.6(MYH9):c.5483+4C>T	MYH9	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 44570	NM_002473.6(MYH9):c.5483+4C>G	MYH9	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 341494	NM_002473.6(MYH9):c.5456T>G (p.Leu1819Arg)	MYH9 (L1819R)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 1620891	NM_002473.6(MYH9):c.5451A>G (p.Ala1817=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3003570	NM_002473.6(MYH9):c.5436C>T (p.Leu1812=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1450149	NM_002473.6(MYH9):c.5431G>A (p.Ala1811Thr)	MYH9 (A1811T)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +3 more	GConflicting classifications of pathogenicity
Select item 756916	NM_002473.6(MYH9):c.5430C>T (p.Thr1810=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962791	NM_002473.6(MYH9):c.5428A>G (p.Thr1810Ala)	MYH9 (T1810A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1911661	NM_002473.6(MYH9):c.5424C>T (p.Ser1808=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978550	NM_002473.6(MYH9):c.5412G>A (p.Lys1804=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1917746	NM_002473.6(MYH9):c.5406G>A (p.Lys1802=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1562686	NM_002473.6(MYH9):c.5394G>A (p.Glu1798=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 902509	NM_002473.6(MYH9):c.5378A>G (p.Lys1793Arg)	MYH9 (K1793R)	Single nucleotide variant (missense variant)	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss +4 more	GConflicting classifications of pathogenicity
Select item 2718714	NM_002473.6(MYH9):c.5374G>A (p.Val1792Ile)	MYH9 (V1792I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2267772	NM_002473.6(MYH9):c.5361C>A (p.Asn1787Lys)	MYH9 (N1787K)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2192040	NM_002473.6(MYH9):c.5360A>G (p.Asn1787Ser)	MYH9 (N1787S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 1368144	NM_002473.6(MYH9):c.5339_5341del (p.Arg1780del)	MYH9 (R1780del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 666863	NM_002473.6(MYH9):c.5338C>T (p.Arg1780Trp)	MYH9 (R1780W)	Single nucleotide variant (missense variant)	Nephrotic syndrome +5 more	GConflicting classifications of pathogenicity
Select item 1940351	NM_002473.6(MYH9):c.5331G>A (p.Glu1777=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1966121	NM_002473.6(MYH9):c.5329G>A (p.Glu1777Lys)	MYH9 (E1777K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1611570	NM_002473.6(MYH9):c.5328C>T (p.Asn1776=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 44569	NM_002473.6(MYH9):c.5323A>G (p.Lys1775Glu)	MYH9 (K1775E)	Single nucleotide variant (missense variant)	MYH9-related disorder +3 more	GLikely benign
Select item 2142338	NM_002473.6(MYH9):c.5317G>A (p.Ala1773Thr)	MYH9 (A1773T)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1965111	NM_002473.6(MYH9):c.5316C>T (p.His1772=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1361814	NM_002473.6(MYH9):c.5314C>T (p.His1772Tyr)	MYH9 (H1772Y)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1305825	NM_002473.6(MYH9):c.5309G>T (p.Arg1770Leu)	MYH9 (R1770L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 545478	NM_002473.6(MYH9):c.5308C>T (p.Arg1770Cys)	MYH9 (R1770C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2009966	NM_002473.6(MYH9):c.5301C>T (p.Asn1767=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2653100	NM_002473.6(MYH9):c.5292C>T (p.Thr1764=)	MYH9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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