ClinVar for Gene (Select 6336) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3600301	NM_006514.4(SCN10A):c.12dup (p.Ile5fs)	SCN10A (I5fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 3589160	NM_006514.4(SCN10A):c.4232A>G (p.Asn1411Ser)	SCN10A (N1411S +2 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2	GUncertain significance
Select item 3438175	NM_006514.4(SCN10A):c.4436A>G (p.Asp1479Gly)	SCN10A (D1479G +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438174	NM_006514.4(SCN10A):c.449C>T (p.Thr150Ile)	SCN10A (T150I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438173	NM_006514.4(SCN10A):c.2162C>G (p.Pro721Arg)	SCN10A (P721R +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438172	NM_006514.4(SCN10A):c.3680A>T (p.Asn1227Ile)	SCN10A (N1226I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438171	NM_006514.4(SCN10A):c.3781C>G (p.Leu1261Val)	SCN10A (L1163V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438170	NM_006514.4(SCN10A):c.3736A>G (p.Ile1246Val)	SCN10A (I1246V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438169	NM_006514.4(SCN10A):c.3531C>A (p.Asp1177Glu)	SCN10A (D1177E +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438168	NM_006514.4(SCN10A):c.1583G>A (p.Gly528Glu)	SCN10A (G528E)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3438167	NM_006514.4(SCN10A):c.5692A>G (p.Thr1898Ala)	SCN10A (T1800A +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438166	NM_006514.4(SCN10A):c.2575G>A (p.Glu859Lys)	SCN10A (E859K +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438165	NM_006514.4(SCN10A):c.721C>A (p.His241Asn)	SCN10A (H241N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3438164	NM_006514.4(SCN10A):c.737T>G (p.Leu246Arg)	SCN10A (L246R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438163	NM_006514.4(SCN10A):c.2271C>T (p.Ser757=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438162	NM_006514.4(SCN10A):c.982A>G (p.Thr328Ala)	SCN10A (T328A)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438161	NM_006514.4(SCN10A):c.4535A>G (p.Asn1512Ser)	SCN10A (N1511S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438158	NM_006514.4(SCN10A):c.4761C>T (p.Ile1587=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438157	NM_006514.4(SCN10A):c.2458A>T (p.Ile820Phe)	SCN10A (I722F +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438156	NM_006514.4(SCN10A):c.4673C>G (p.Ala1558Gly)	SCN10A (A1460G +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438155	NM_006514.4(SCN10A):c.249T>G (p.Asp83Glu)	SCN10A (D83E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438154	NM_006514.4(SCN10A):c.4181T>C (p.Met1394Thr)	SCN10A (M1394T +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438153	NM_006514.4(SCN10A):c.2153C>T (p.Ala718Val)	SCN10A (A620V +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438152	NM_006514.4(SCN10A):c.4929C>T (p.Asn1643=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438151	NM_006514.4(SCN10A):c.1929G>A (p.Leu643=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438150	NM_006514.4(SCN10A):c.4279A>T (p.Lys1427Ter)	SCN10A (K1329* +2 more)	Single nucleotide variant (nonsense)	Cardiovascular phenotype	GUncertain significance
Select item 3438148	NM_006514.4(SCN10A):c.2358A>T (p.Ala786=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438147	NM_006514.4(SCN10A):c.2427A>G (p.Leu809=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438146	NM_006514.4(SCN10A):c.2334G>A (p.Lys778=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438145	NM_006514.4(SCN10A):c.2325A>G (p.Thr775=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438144	NM_006514.4(SCN10A):c.2457T>A (p.Asn819Lys)	SCN10A (N721K +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3438143	NM_006514.4(SCN10A):c.4345T>C (p.Leu1449=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438142	NM_006514.4(SCN10A):c.2352G>C (p.Val784=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438141	NM_006514.4(SCN10A):c.2448C>G (p.Asn816Lys)	SCN10A (N816K +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438140	NM_006514.4(SCN10A):c.2442T>C (p.Arg814=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438139	NM_006514.4(SCN10A):c.2313C>A (p.Pro771=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438138	NM_006514.4(SCN10A):c.2349A>G (p.Ser783=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438137	NM_006514.4(SCN10A):c.2343A>C (p.Gly781=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438136	NM_006514.4(SCN10A):c.2443A>C (p.Asn815His)	SCN10A (N815H +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438135	NM_006514.4(SCN10A):c.2451A>G (p.Arg817=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438134	NM_006514.4(SCN10A):c.5154T>C (p.Ile1718=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438133	NM_006514.4(SCN10A):c.2397T>C (p.Phe799=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438132	NM_006514.4(SCN10A):c.4252A>C (p.Ile1418Leu)	SCN10A (I1320L +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438131	NM_006514.4(SCN10A):c.2312C>G (p.Pro771Arg)	SCN10A (P673R +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438130	NM_006514.4(SCN10A):c.5115C>T (p.Tyr1705=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438129	NM_006514.4(SCN10A):c.540T>C (p.Asn180=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438128	NM_006514.4(SCN10A):c.4178A>G (p.Tyr1393Cys)	SCN10A (Y1392C +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438127	NM_006514.4(SCN10A):c.4518A>G (p.Lys1506=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438126	NM_006514.4(SCN10A):c.5291T>C (p.Leu1764Pro)	SCN10A (L1666P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438125	NM_006514.4(SCN10A):c.3124C>T (p.His1042Tyr)	LOC110121288, SCN10A (H1042Y +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438124	NM_006514.4(SCN10A):c.4215A>G (p.Gly1405=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438123	NM_006514.4(SCN10A):c.2566G>A (p.Ala856Thr)	SCN10A (A758T +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438122	NM_006514.4(SCN10A):c.3918G>A (p.Lys1306=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438121	NM_006514.4(SCN10A):c.4653T>C (p.Ile1551=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438120	NM_006514.4(SCN10A):c.5160G>A (p.Val1720=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438119	NM_006514.4(SCN10A):c.314G>A (p.Ser105Asn)	SCN10A (S105N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438118	NM_006514.4(SCN10A):c.3771A>G (p.Pro1257=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438117	NM_006514.4(SCN10A):c.1499G>C (p.Ser500Thr)	SCN10A (S500T)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3438116	NM_006514.4(SCN10A):c.4917C>A (p.Asp1639Glu)	SCN10A (D1639E +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438115	NM_006514.4(SCN10A):c.2156T>G (p.Phe719Cys)	SCN10A (F719C +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438114	NM_006514.4(SCN10A):c.5339C>A (p.Pro1780His)	SCN10A (P1682H +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438113	NM_006514.4(SCN10A):c.2471A>T (p.His824Leu)	SCN10A (H824L +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438112	NM_006514.4(SCN10A):c.3140G>T (p.Ser1047Ile)	LOC110121288, SCN10A (S1047I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438111	NM_006514.4(SCN10A):c.5009T>A (p.Ile1670Asn)	SCN10A (I1572N +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438110	NM_006514.4(SCN10A):c.2398G>T (p.Val800Phe)	SCN10A (V800F +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438109	NM_006514.4(SCN10A):c.449C>A (p.Thr150Asn)	SCN10A (T150N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438108	NM_006514.4(SCN10A):c.3264G>C (p.Thr1088=)	LOC110121288, SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438107	NM_006514.4(SCN10A):c.837T>A (p.Asn279Lys)	SCN10A (N279K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438106	NM_006514.4(SCN10A):c.5164C>A (p.Leu1722Met)	SCN10A (L1721M +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438105	NM_006514.4(SCN10A):c.1729C>T (p.Leu577Phe)	SCN10A (L577F)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3438104	NM_006514.4(SCN10A):c.5660C>T (p.Ala1887Val)	SCN10A (A1886V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3438103	NM_006514.4(SCN10A):c.5317G>C (p.Gly1773Arg)	SCN10A (G1675R +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438102	NM_006514.4(SCN10A):c.537A>C (p.Leu179=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438101	NM_006514.4(SCN10A):c.4157C>A (p.Pro1386His)	SCN10A (P1386H +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438100	NM_006514.4(SCN10A):c.5454G>T (p.Leu1818Phe)	SCN10A (L1720F +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438099	NM_006514.4(SCN10A):c.2418G>A (p.Lys806=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438098	NM_006514.4(SCN10A):c.4082T>C (p.Leu1361Pro)	SCN10A (L1360P +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438097	NM_006514.4(SCN10A):c.3885C>G (p.Phe1295Leu)	SCN10A (F1197L +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438096	NM_006514.4(SCN10A):c.4973C>T (p.Thr1658Ile)	SCN10A (T1658I +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438095	NM_006514.4(SCN10A):c.5675A>G (p.Glu1892Gly)	SCN10A (E1794G +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438094	NM_006514.4(SCN10A):c.931G>A (p.Gly311Ser)	SCN10A (G311S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438093	NM_006514.4(SCN10A):c.1346C>T (p.Pro449Leu)	SCN10A (P449L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438092	NM_006514.4(SCN10A):c.3192G>C (p.Thr1064=)	LOC110121288, SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438091	NM_006514.4(SCN10A):c.5266A>T (p.Thr1756Ser)	SCN10A (T1755S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438090	NM_006514.4(SCN10A):c.5203C>G (p.Pro1735Ala)	SCN10A (P1735A +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438089	NM_006514.4(SCN10A):c.3876G>T (p.Trp1292Cys)	SCN10A (W1292C +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438088	NM_006514.4(SCN10A):c.1341A>G (p.Gly447=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438087	NM_006514.4(SCN10A):c.4836G>A (p.Leu1612=)	SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3438084	NM_006514.4(SCN10A):c.5021G>T (p.Gly1674Val)	SCN10A (G1674V +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438083	NM_006514.4(SCN10A):c.5020G>A (p.Gly1674Arg)	SCN10A (G1576R +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438081	NM_006514.4(SCN10A):c.80A>G (p.Gln27Arg)	SCN10A (Q27R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3438080	NM_006514.4(SCN10A):c.4399G>A (p.Gly1467Ser)	SCN10A (G1466S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3438079	NM_006514.4(SCN10A):c.2011A>G (p.Ile671Val)	SCN10A (I573V +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3390031	NM_006514.4(SCN10A):c.5638C>A (p.Pro1880Thr)	SCN10A (P1782T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3388463	NM_006514.4(SCN10A):c.4485G>A (p.Val1495=)	SCN10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3379450	NM_006514.4(SCN10A):c.3985A>C (p.Lys1329Gln)	SCN10A (K1231Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3370977	NM_006514.4(SCN10A):c.5128T>C (p.Phe1710Leu)	SCN10A (F1612L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368872	NM_006514.4(SCN10A):c.4507G>A (p.Glu1503Lys)	SCN10A (E1405K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368470	NM_006514.4(SCN10A):c.3631A>G (p.Lys1211Glu)	SCN10A (K1113E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368220	NM_006514.4(SCN10A):c.428A>C (p.Asn143Thr)	SCN10A (N143T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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