Transcript #00000055 (NM_001165963.2, SCN1A gene)

Transcript name transcript variant 1
Gene name SCN1A (sodium voltage-gated channel alpha subunit 1)
Chromosome 2
Transcript - NCBI ID NM_001165963.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001159435.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

56 entries on 1 page. Showing entries 1 - 56.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 1 c.247T>G - r.(?) p.(Tyr83Asp) - -
+/. - c.265-699A>G - r.(=) p.(=) - -
?/. - c.280A>C - r.(?) p.(Asn94His) - ClinVar
+/. - c.424T>C - r.(?) p.(Cys142Arg) - -
+/. - c.506C>G - r.(?) p.(Ser169*) - -
+/. - c.602+1G>A - r.spl? p.? - -
+/. - c.603-91G>A - r.(=) p.(=) - drug response
+/. - c.603-91G>A - r.(=) p.(=) - drug response
+/. - c.603-91G>A - r.(=) p.(=) - drug response
+/. - c.603-91G>A - r.(=) p.(=) - -
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.603-91G>A - r.(=) p.(=) - ClinVar
+/. - c.654_655delCA - r.(?) p.(Phe218Leufs*58) - -
+/. - c.838T>C - r.(?) p.(Trp280Arg) - ClinVar
+/. - c.942G>A - r.(?) p.(Trp314*) - -
+/. - c.1034G>A - r.(?) p.(Cys345Tyr) - ClinVar
-/. 8 c.1152G>A - r.(?) p.(Trp384*) - ClinVar
+/. 9 c.1177C>T - r.(?) p.(Arg393Cys) - ClinVar
+/. 9 c.1259C>T - r.(?) p.(Ala420Val) - ClinVar
+/. - c.1377+1G>A - r.spl? p.? - -
+/. 11 c.1702C>T - r.(?) p.(Arg568*) - ClinVar
+/. - c.1813_1814del - r.(?) p.(Asp606Phefs*21) - -
+/. - c.2068_2069insT - r.(?) p.(Arg690Metfs*39) - -
+/. 12 c.2134C>T - r.(?) p.(Arg712*) - ClinVar
+/. 12 c.2173G>A - r.(?) p.(Glu725Lys) - -
+/. - c.2415+2T>A - r.spl? p.? - -
+/. 14 c.2439A>T - r.(=) p.(=) - -
+/. - c.2589+3A>T - r.spl? p.? - ClinVar
+/. 15 c.2643G>C - r.(?) p.(Lys881Asn) - -
+/. - c.2836C>T - r.(?) p.(Arg946Cys) - -
+/. - c.2837G>A - r.(?) p.(Arg946His) - -
+/. - c.3079A>T - r.(?) p.(Lys1027*) - -
?/. 16 c.3099delT - r.(?) p.(Phe1033Leufs*13) - ClinVar
+/. - c.3199G>C - r.(?) p.(Ala1067Pro) - Benign
+/. - c.3829C>T - r.(?) p.(Gln1277*) - -
+/. 20 c.3943_3949del - r.(?) p.(Leu1315Hisfs*2) - -
+/. - c.4072T>C - r.(?) p.(Trp1358Arg) - -
+/. 22 c.4324G>C - r.(?) p.(Val1442Leu) - -
+/. 24 c.4547C>A - r.(?) p.(Ser1516*) - ClinVar
+/. 25 c.4649T>G - r.(?) p.(Leu1550Arg) - -
+/. - c.4786_4788delCGC - r.(?) p.(Arg1596del) - -
+/. 25 c.4790A>G - r.(?) p.(His1597Arg) - -
+/. 26 c.4906C>T - r.(?) p.(Arg1636*) - ClinVar
+/. 26 c.5129T>G - r.(?) p.(Phe1710Cys) - ClinVar
+/. 26 c.5155C>T - r.(?) p.(Gln1719*) - -
+/. 26 c.5197A>G - r.(?) p.(Ile1733Val) - -
+/. 26 c.5230A>G - r.(?) p.(Asn1744Asp) - -
+/. - c.5345T>C - r.(?) p.(Ile1782Thr) - -
+/. 26 c.5656C>T - r.(?) p.(Arg1886*) - ClinVar
+/. - c.5734C>T - r.(?) p.(Arg1912*) - ClinVar
+/. 26 c.5753C>T - r.(?) p.(Ser1918Phe) - Likely Pathogenic
+/. 26 c.5788delC - r.(?) p.(Leu1930Phefs*2) - -
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