Transcript #00025619 (NM_014191.3, SCN8A gene)

Transcript name transcript variant 1
Gene name SCN8A (sodium channel, voltage gated, type VIII, alpha subunit)
Chromosome 12
Transcript - NCBI ID NM_014191.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_055006.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2021-05-28 11:43:18 +02:00 (CEST)
Date last edited N/A


Variants

329 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. 27 c.? r.? p.?
?/. 2 c.? r.? p.?
?/. 5 c.? r.? p.?
?/. 7 c.? r.? p.?
?/. 12 c.? r.? p.?
?/. 13 c.? r.? p.?
?/. - c.10C>T r.(?) p.(Arg4Trp)
?/. - c.53C>A r.(?) p.(Thr18Asn)
-?/. - c.95G>A r.(?) p.(Ser32Asn)
-?/. - c.95G>A r.(?) p.(Ser32Asn)
?/. - c.269C>T r.(?) p.(Thr90Met)
-?/. - c.270G>T r.(?) p.(Thr90=)
?/. - c.272A>C r.(?) p.(Gln91Pro)
-?/. - c.327G>A r.(?) p.(Thr109=)
-?/. - c.389T>C r.(?) p.(Ile130Thr)
-?/. - c.396-6C>T r.(=) p.(=)
+?/. - c.415A>C r.(?) p.(Met139Leu)
-?/. - c.508A>T r.(?) p.(Thr170Ser)
-/. - c.576C>T r.(?) p.(Asp192=)
-/. - c.576C>T r.(?) p.(Asp192=)
-/. - c.576C>T r.(?) p.(Asp192=)
?/. - c.599G>A r.(?) p.(Ser200Asn)
?/. - c.614+1G>A r.spl? p.?
?/. - c.615-3C>G r.spl? p.?
?/. - c.619A>G r.(?) p.(Ile207Val)
+/. - c.641G>A r.(?) p.(Gly214Asp)
+?/. - c.641G>A r.(?) p.(Gly214Asp)
+/. - c.643A>G - -
+/. 7 c.647T>A r.(?) p.(Val216Asp)
?/. - c.658C>T r.(?) p.(Arg220Cys)
-?/. - c.658C>T r.(?) p.(Arg220Cys)
+/. - c.667A>G r.(?) p.(Arg223Gly)
?/. - c.686A>G r.(?) p.(Lys229Arg)
+/. - c.697G>C r.(?) p.(Val233Leu)
-?/. - c.706+5G>T r.spl? p.?
-?/. - c.706+5G>T r.spl? p.?
-?/. - c.706+5G>T r.spl? p.?
?/. - c.706+238G>A r.(=) p.(=)
+?/. - c.706+238G>A r.(=) p.(=)
-?/. - c.706+256A>T r.(=) p.(=)
-?/. - c.707-20C>T r.(=) p.(=)
-?/. - c.707-20C>T r.(=) p.(=)
?/. - c.728C>T r.(?) p.(Ala243Val)
?/. - c.740C>A r.(?) p.(Ser247Tyr)
-?/. - c.744G>A r.(?) p.(Val248=)
-?/. - c.751C>T r.(?) p.(Leu251=)
+?/. - c.752T>C r.(?) p.(Leu251Pro)
+/. - c.779T>C r.(?) p.(Phe260Ser)
+?/. - c.800T>C r.(?) p.(Leu267Ser)
-?/. - c.810G>A r.(?) p.(Leu270=)
-?/. - c.928+9C>T r.(=) p.(=)
?/. - c.929-4C>G - -
-?/. - c.975G>A r.(?) p.(Gly325=)
+?/. - c.979A>C r.(?) p.(Ser327Arg)
?/. - c.1020G>A r.(?) p.(Met340Ile)
-?/. - c.1026A>T r.(?) p.(Ala342=)
?/. - c.1200C>A r.(?) p.(Phe400Leu)
+?/. - c.1215del r.(?) p.(Ile406SerfsTer58)
+/. - c.1219T>G r.(?) p.(Leu407Val)
?/. - c.1330G>T r.(?) p.(Glu444*)
-?/. - c.1349C>T r.(?) p.(Ala450Val)
+?/. - c. 1391A>G r.(?) p.Glu464Ala
-?/. - c.1416C>T r.(?) p.(=)
?/. - c.1450A>G r.(?) p.(Ser484Gly)
?/. - c.1460G>T r.(?) p.(Ser487Ile)
-?/. - c.1470A>G r.(?) p.(Glu490=)
-?/. - c.1470A>G r.(?) p.(Glu490=)
-?/. - c.1509C>A r.(?) p.(Leu503=)
?/. - c.1529G>A r.(?) p.(Gly510Glu)
-?/. - c.1534C>T r.(?) p.(Pro512Ser)
+/. - c.1588C>T - -
-?/. - c.1620T>C r.(?) p.(Phe540=)
+?/. - c.1622C>A - -
?/. - c.1651_1695dup r.(?) p.(Pro551_Ile565dup)
?/. - c.1717C>T - -
+?/. 12 c.1723C>T r.? p.?
-?/. - c.1740G>A r.(?) p.(Glu580=)
?/. - c.1769C>T r.(?) p.(Thr590Met)
-?/. - c.1779G>C r.(?) p.(Glu593Asp)
-?/. - c.1779G>C r.(?) p.(Glu593Asp)
?/. - c.1779G>C r.(?) p.(Glu593Asp)
+?/. - c.1790G>A r.(?) p.(Arg597His)
?/. - c.1796A>T r.(?) p.(Asp599Val)
-?/. - c.1819G>A r.(?) p.(Ala607Thr)
-?/. - c.1819G>A r.(?) p.(Ala607Thr)
?/. - c.1829G>C r.(?) p.(Arg610Pro)
-?/. - c.1833G>T r.(?) p.(Arg611=)
+/. - c.1849dup r.(?) p.(Tyr617LeufsTer54)
?/. - c.1855_1863del r.(?) p.(Gly619_Ser621del)
?/. - c.1855_1863del r.(?) p.(Gly619_Ser621del)
?/. - c.1876T>A r.(?) p.(Ser626Thr)
?/. - c.1876T>C r.(?) p.(Ser626Pro)
-?/. - c.1890C>G r.(?) p.(Phe630Leu)
?/. - c.1938C>A r.(?) p.(Asn646Lys)
-?/. - c.1963C>T r.(?) p.(Pro655Ser)
-?/. - c.1965C>T r.(?) p.(=)
?/. - c.1984C>T r.(?) p.(Arg662Cys)
-/. - c.1999-5del r.spl? p.?
-/. - c.1999-5dup r.spl? p.?
-?/. - c.1999-5T>A r.spl? p.?
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