Transcript #00018527 (NM_014139.2, SCN11A gene)

Transcript name sodium channel, voltage-gated, type XI, alpha subunit
Gene name SCN11A (sodium channel, voltage-gated, type XI, alpha subunit)
Chromosome 3
Transcript - NCBI ID NM_014139.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_054858.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

275 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-28G>C r.(?) p.(=)
?/. - c.19C>G r.(?) p.(Pro7Ala)
-?/. - c.19C>G r.(?) p.(Pro7Ala)
-?/. - c.95C>T r.(?) p.(Ala32Val)
-?/. - c.95C>T r.(?) p.(Ala32Val)
?/. - c.151C>T r.(?) p.(Arg51Trp)
-?/. - c.153G>T r.(?) p.(Arg51=)
-?/. - c.160C>T r.(?) p.(Leu54Phe)
-?/. - c.201C>T r.(?) p.(Gly67=)
-/. - c.256C>A r.(?) p.(Arg86=)
-?/. - c.256C>G r.(?) p.(Arg86Gly)
-?/. - c.267+9T>C r.(=) p.(=)
-/. - c.267+14_267+17dup r.(=) p.(=)
-/. - c.267+16G>C r.(=) p.(=)
-?/. - c.267+17_267+18insC r.(=) p.(=)
-?/. - c.267+17_267+18insCG r.(=) p.(=)
-/. - c.267+17_267+18insCGG r.(=) p.(=)
-?/. - c.267+18G>A r.(=) p.(=)
-/. - c.267+18G>C r.(=) p.(=)
-/. - c.267+19G>C r.(=) p.(=)
-/. - c.267+20G>T r.(=) p.(=)
-/. - c.267+20_267+21insT r.(=) p.(=)
-/. - c.267+22_267+38del r.(=) p.(=)
-/. - c.268-10dup r.(=) p.(=)
-/. - c.268-10dup r.(=) p.(=)
-?/. - c.268-3C>T r.spl? p.?
-?/. - c.268-3C>T r.spl? p.?
-?/. - c.268-3C>T r.spl? p.?
-?/. - c.268-3C>T r.spl? p.?
-?/. - c.268-3C>T r.spl? p.?
-?/. - c.276G>T r.(?) p.(Met92Ile)
?/. - c.277G>A r.(?) p.(Val93Met)
?/. - c.327G>T r.(?) p.(Leu109Phe)
-?/. - c.386+8T>C r.(=) p.(=)
-?/. - c.387-12G>T r.(=) p.(=)
-?/. - c.408C>T r.(?) p.(Ile136=)
-?/. - c.462C>T r.(?) p.(Ser154=)
?/. - c.494_501dup r.(?) p.(Gly168Serfs*11)
?/. - c.499A>T r.(?) p.(Thr167Ser)
?/. - c.547T>G r.(?) p.(Phe183Val)
?/. - c.575G>A r.(?) p.(Arg192Gln)
?/. - c.604G>T r.(?) p.(Val202Phe)
?/. - c.673C>T r.(?) p.(Arg225Cys)
?/. - c.695C>T r.(?) p.(Ala232Val)
?/. - c.712C>T r.(?) p.(Arg238Cys)
-?/. - c.712C>T r.(?) p.(Arg238Cys)
-/. - c.713-12C>A r.(=) p.(=)
-/. - c.713-12C>A r.(=) p.(=)
-/. - c.757C>T r.(?) p.(Leu253=)
-/. - c.757C>T r.(?) p.(Leu253=)
-/. - c.757C>T r.(?) p.(Leu253=)
-?/. - c.760G>T r.(?) p.(Val254Phe)
-?/. - c.807G>A r.(?) p.(Leu269=)
-?/. - c.865A>G r.(?) p.(Lys289Glu)
-?/. - c.881C>T r.(?) p.(Pro294Leu)
-?/. - c.892+24C>T r.(=) p.(=)
-?/. - c.959+5G>A r.spl? p.?
?/. - c.988C>A r.(?) p.(His330Asn)
-?/. - c.998T>G r.(?) p.(Ile333Ser)
?/. - c.1060C>T r.(?) p.(Arg354Trp)
+?/. - c.1060C>T r.(?) p.(Arg354Trp)
-/. - c.1062G>A r.(?) p.(Arg354=)
?/. - c.1070C>T r.(?) p.(Thr357Ile)
-?/. - c.1097A>G r.(?) p.(Gln366Arg)
-?/. - c.1097A>G r.(?) p.(Gln366Arg)
-?/. - c.1102-5T>C r.spl? p.?
?/. - c.1138_1140del r.(?) p.(Phe380del)
+?/. - c.1142T>C r.(?) p.(Ile381Thr)
?/. - c.1142T>C r.(?) p.(Ile381Thr)
?/. - c.1172T>G r.(?) p.(Leu391Arg)
+?/. - c.1187T>C r.(?) p.(Leu396Pro)
?/. - c.1220A>G r.(?) p.(Asn407Ser)
-?/. - c.1257G>T r.(?) p.(Lys419Asn)
?/. - c.1257G>T r.(?) p.(Lys419Asn)
-?/. - c.1300-18C>G r.(=) p.(=)
-?/. - c.1300-18C>G r.(=) p.(=)
?/. - c.1399A>G r.(?) p.(Lys467Glu)
-/. - c.1442G>A r.(?) p.(Gly481Glu)
-/. - c.1442G>A r.(?) p.(Gly481Glu)
-/. - c.1442G>A r.(?) p.(Gly481Glu)
-/. - c.1473+12C>T r.(=) p.(=)
-?/. - c.1473+12C>T r.(=) p.(=)
-?/. - c.1501C>T r.(?) p.(Leu501=)
-?/. - c.1566A>G r.(?) p.(Ala522=)
-?/. - c.1575T>C r.(?) p.(Ala525=)
?/. - c.1599G>A r.(?) p.(Met533Ile)
-?/. - c.1604-18T>C r.(=) p.(=)
-?/. - c.1632C>A r.(?) p.(=)
-/. - c.1638T>C r.(?) p.(Cys546=)
-?/. - c.1681C>T r.(?) p.(Pro561Ser)
-?/. - c.1683C>A r.(?) p.(Pro561=)
-?/. - c.1696G>A r.(?) p.(Val566Ile)
?/. - c.1744G>A r.(?) p.(Ala582Thr)
-?/. - c.1843-39C>T r.(=) p.(=)
-?/. - c.1843-10C>A r.(=) p.(=)
-?/. - c.1843-10C>A r.(=) p.(=)
-?/. - c.1843-10C>A r.(=) p.(=)
-?/. - c.1843-10C>A r.(=) p.(=)
-?/. - c.1843-4C>T r.spl? p.?
?/. - c.1913G>A r.(?) p.(Arg638His)
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