"Ambry Genetics"[submitter] AND "SCN10A"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 463270	NM_006514.4(SCN10A):c.5866C>A (p.Pro1956Thr)	SCN10A (P1956T +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2563719	NM_006514.4(SCN10A):c.5858C>G (p.Ala1953Gly)	SCN10A (A1952G +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 852767	NM_006514.4(SCN10A):c.5858C>T (p.Ala1953Val)	SCN10A (A1952V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1750038	NM_006514.4(SCN10A):c.5846T>A (p.Met1949Lys)	SCN10A (M1949K +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 391439	NM_006514.4(SCN10A):c.5834A>G (p.Glu1945Gly)	SCN10A (E1945G +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GBenign/Likely benign
Select item 834159	NM_006514.4(SCN10A):c.5820A>G (p.Ile1940Met)	SCN10A (I1842M +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 2448840	NM_006514.4(SCN10A):c.5809T>C (p.Ser1937Pro)	SCN10A (S1936P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1749801	NM_006514.4(SCN10A):c.5804G>A (p.Arg1935Lys)	SCN10A (R1934K +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 757184	NM_006514.4(SCN10A):c.5789A>T (p.Asp1930Val)	SCN10A (D1832V +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GLikely benign
Select item 1749613	NM_006514.4(SCN10A):c.5781C>A (p.Gly1927=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749588	NM_006514.4(SCN10A):c.5779G>A (p.Gly1927Ser)	SCN10A (G1926S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1749575	NM_006514.4(SCN10A):c.5775T>G (p.Thr1925=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749569	NM_006514.4(SCN10A):c.5774C>T (p.Thr1925Ile)	SCN10A (T1924I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1516375	NM_006514.4(SCN10A):c.5764G>A (p.Glu1922Lys)	SCN10A (E1824K +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GConflicting classifications of pathogenicity
Select item 837765	NM_006514.4(SCN10A):c.5762A>T (p.Tyr1921Phe)	SCN10A (Y1920F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 391298	NM_006514.4(SCN10A):c.5757G>A (p.Pro1919=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +2 more	GLikely benign
Select item 1749359	NM_006514.4(SCN10A):c.5739T>G (p.Ser1913=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749345	NM_006514.4(SCN10A):c.5734G>T (p.Ala1912Ser)	SCN10A (A1912S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1749336	NM_006514.4(SCN10A):c.5732C>G (p.Thr1911Ser)	SCN10A (T1910S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1749295	NM_006514.4(SCN10A):c.5724A>G (p.Lys1908=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749249	NM_006514.4(SCN10A):c.5711T>C (p.Val1904Ala)	SCN10A (V1904A +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1040345	NM_006514.4(SCN10A):c.5700T>A (p.Asn1900Lys)	SCN10A (N1802K +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 567996	NM_006514.4(SCN10A):c.5694del (p.Ala1899fs)	SCN10A (A1899fs +2 more)	Deletion (frameshift variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2448846	NM_006514.4(SCN10A):c.5685T>A (p.Val1895=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749049	NM_006514.4(SCN10A):c.5685T>C (p.Val1895=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1749042	NM_006514.4(SCN10A):c.5683G>T (p.Val1895Phe)	SCN10A (V1895F +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1571856	NM_006514.4(SCN10A):c.5682T>C (p.Phe1894=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 959059	NM_006514.4(SCN10A):c.5671G>T (p.Asp1891Tyr)	SCN10A (D1891Y +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1138637	NM_006514.4(SCN10A):c.5661A>G (p.Ala1887=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GLikely benign
Select item 1639613	NM_006514.4(SCN10A):c.5658T>C (p.Ala1886=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GLikely benign
Select item 95405	NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val)	SCN10A (A1886V +2 more)	Single nucleotide variant (missense variant)	SCN10A-related condition +4 more	GBenign/Likely benign
Select item 941023	NM_006514.4(SCN10A):c.5630C>T (p.Pro1877Leu)	SCN10A (P1779L +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 700494	NM_006514.4(SCN10A):c.5628C>G (p.Thr1876=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GBenign/Likely benign
Select item 391917	NM_006514.4(SCN10A):c.5626A>G (p.Thr1876Ala)	SCN10A (T1876A +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 849172	NM_006514.4(SCN10A):c.5613G>A (p.Met1871Ile)	SCN10A (M1773I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1748635	NM_006514.4(SCN10A):c.5611A>G (p.Met1871Val)	SCN10A (M1870V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1401218	NM_006514.4(SCN10A):c.5606G>A (p.Arg1869His)	SCN10A (R1771H +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 420024	NM_006514.4(SCN10A):c.5605C>T (p.Arg1869Cys)	SCN10A (R1869C +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 1103908	NM_006514.4(SCN10A):c.5604C>T (p.His1868=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 463269	NM_006514.4(SCN10A):c.5603A>C (p.His1868Pro)	SCN10A (H1868P +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GLikely benign
Select item 655331	NM_006514.4(SCN10A):c.5600T>G (p.Leu1867Arg)	SCN10A (L1769R +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1748504	NM_006514.4(SCN10A):c.5594A>C (p.Tyr1865Ser)	SCN10A (Y1767S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 958796	NM_006514.4(SCN10A):c.5594A>G (p.Tyr1865Cys)	SCN10A (Y1767C +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 414635	NM_006514.4(SCN10A):c.5589G>A (p.Arg1863=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GLikely benign
Select item 1380283	NM_006514.4(SCN10A):c.5588G>A (p.Arg1863Gln)	SCN10A (R1765Q +2 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +2 more	GUncertain significance
Select item 1020384	NM_006514.4(SCN10A):c.5587C>T (p.Arg1863Trp)	SCN10A (R1765W +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 1748431	NM_006514.4(SCN10A):c.5581G>T (p.Ala1861Ser)	SCN10A (A1860S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2448850	NM_006514.4(SCN10A):c.5563G>C (p.Ala1855Pro)	SCN10A (A1855P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1748311	NM_006514.4(SCN10A):c.5560T>C (p.Ser1854Pro)	SCN10A (S1756P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1748255	NM_006514.4(SCN10A):c.5554G>C (p.Asp1852His)	SCN10A (D1754H +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1163442	NM_006514.4(SCN10A):c.5548C>G (p.Gln1850Glu)	SCN10A (Q1752E +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 430247	NM_006514.4(SCN10A):c.5548C>T (p.Gln1850Ter)	SCN10A (Q1850* +2 more)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 463268	NM_006514.4(SCN10A):c.5540G>A (p.Arg1847Gln)	SCN10A (R1847Q +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 452050	NM_006514.4(SCN10A):c.5539C>T (p.Arg1847Ter)	SCN10A (R1847* +2 more)	Single nucleotide variant (nonsense)	Episodic pain syndrome, familial, 2 +3 more	GUncertain significance
Select item 240681	NM_006514.4(SCN10A):c.5523A>G (p.Pro1841=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2448863	NM_006514.4(SCN10A):c.5520A>C (p.Glu1840Asp)	SCN10A (E1839D +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 938480	NM_006514.4(SCN10A):c.5516A>G (p.Tyr1839Cys)	SCN10A (Y1838C +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 1748017	NM_006514.4(SCN10A):c.5509T>C (p.Ser1837Pro)	SCN10A (S1739P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 463267	NM_006514.4(SCN10A):c.5496T>C (p.Thr1832=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GBenign/Likely benign
Select item 660254	NM_006514.4(SCN10A):c.5476GAG[1] (p.Glu1827del)	SCN10A (E1827del +2 more)	Microsatellite (inframe_deletion)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 2448830	NM_006514.4(SCN10A):c.5480A>T (p.Glu1827Val)	SCN10A (E1729V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 864708	NM_006514.4(SCN10A):c.5479G>A (p.Glu1827Lys)	SCN10A (E1826K +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1747764	NM_006514.4(SCN10A):c.5475G>A (p.Met1825Ile)	SCN10A (M1727I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1551468	NM_006514.4(SCN10A):c.5461C>T (p.Leu1821=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 463266	NM_006514.4(SCN10A):c.5451G>A (p.Glu1817=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1213376	NM_006514.4(SCN10A):c.5446G>A (p.Gly1816Arg)	SCN10A (G1718R +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 390115	NM_006514.4(SCN10A):c.5445C>T (p.Ser1815=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1747522	NM_006514.4(SCN10A):c.5437G>A (p.Gly1813Arg)	SCN10A (G1813R +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1552672	NM_006514.4(SCN10A):c.5436A>G (p.Leu1812=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1747465	NM_006514.4(SCN10A):c.5426A>G (p.Lys1809Arg)	SCN10A (K1711R +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1747395	NM_006514.4(SCN10A):c.5417C>T (p.Ala1806Val)	SCN10A (A1708V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1747197	NM_006514.4(SCN10A):c.5387A>G (p.Asp1796Gly)	SCN10A (D1796G +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2310281	NM_006514.4(SCN10A):c.5378T>C (p.Val1793Ala)	SCN10A (V1793A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 463264	NM_006514.4(SCN10A):c.5371C>A (p.Pro1791Thr)	SCN10A (P1791T +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 696364	NM_006514.4(SCN10A):c.5370G>T (p.Leu1790=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 1009585	NM_006514.4(SCN10A):c.5365G>A (p.Asp1789Asn)	SCN10A (D1691N +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1747078	NM_006514.4(SCN10A):c.5363T>C (p.Met1788Thr)	SCN10A (M1788T +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 1747036	NM_006514.4(SCN10A):c.5358C>A (p.Ile1786=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 390781	NM_006514.4(SCN10A):c.5358C>T (p.Ile1786=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1570609	NM_006514.4(SCN10A):c.5343T>C (p.Asn1781=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 532095	NM_006514.4(SCN10A):c.5342A>G (p.Asn1781Ser)	SCN10A (N1781S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1746904	NM_006514.4(SCN10A):c.5337del (p.Lys1779fs)	SCN10A (K1778fs +2 more)	Deletion (frameshift variant)	Cardiovascular phenotype	GUncertain significance
Select item 1706207	NM_006514.4(SCN10A):c.5332C>T (p.Pro1778Ser)	SCN10A (P1680S +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2624441	NM_006514.4(SCN10A):c.5329del (p.Ile1777fs)	SCN10A (I1777fs +2 more)	Deletion (frameshift variant)	Cardiovascular phenotype	GUncertain significance
Select item 1746728	NM_006514.4(SCN10A):c.5307C>T (p.Asp1769=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1217744	NM_006514.4(SCN10A):c.5306A>C (p.Asp1769Ala)	SCN10A (D1671A +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1411583	NM_006514.4(SCN10A):c.5301T>G (p.Phe1767Leu)	SCN10A (F1767L +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 381215	NM_006514.4(SCN10A):c.5295G>A (p.Ser1765=)	SCN10A	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 577180	NM_006514.4(SCN10A):c.5294C>T (p.Ser1765Leu)	SCN10A (S1765L +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GUncertain significance
Select item 1746632	NM_006514.4(SCN10A):c.5290C>T (p.Leu1764Phe)	SCN10A (L1666F +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 532164	NM_006514.4(SCN10A):c.5286T>C (p.Ser1762=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1746589	NM_006514.4(SCN10A):c.5284T>C (p.Ser1762Pro)	SCN10A (S1761P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1746574	NM_006514.4(SCN10A):c.5281T>A (p.Phe1761Ile)	SCN10A (F1760I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1746390	NM_006514.4(SCN10A):c.5257C>T (p.Pro1753Ser)	SCN10A (P1655S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1150029	NM_006514.4(SCN10A):c.5256C>T (p.Asp1752=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2563710	NM_006514.4(SCN10A):c.5254G>A (p.Asp1752Asn)	SCN10A (D1752N +2 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +1 more	GUncertain significance
Select item 572545	NM_006514.4(SCN10A):c.5249A>G (p.Lys1750Arg)	SCN10A (K1750R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1746267	NM_006514.4(SCN10A):c.5239A>G (p.Thr1747Ala)	SCN10A (T1746A +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2448854	NM_006514.4(SCN10A):c.5235T>C (p.Tyr1745=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 240680	NM_006514.4(SCN10A):c.5217C>T (p.Asp1739=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +2 more	GBenign

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