Transcript #00018526 (NM_006514.2, SCN10A gene)

Transcript name sodium channel, voltage-gated, type X, alpha subunit
Gene name SCN10A (sodium channel, voltage-gated, type X, alpha subunit)
Chromosome 3
Transcript - NCBI ID NM_006514.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006505.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

471 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-8A>T r.(?) p.(=)
?/. - c.-8A>T r.(?) p.(=)
?/. - c.23T>C r.(?) p.(Leu8Pro)
-?/. - c.32A>T r.(?) p.(Asn11Ile)
-?/. - c.39C>T r.(?) p.(Phe13=)
?/. - c.40C>T r.(?) p.(Arg14Cys)
-?/. - c.41G>T r.(?) p.(Arg14Leu)
-?/. - c.41G>T r.(?) p.(Arg14Leu)
-?/. - c.41G>T r.(?) p.(Arg14Leu)
-/. - c.45C>T r.(?) p.(Arg15=)
-/. - c.45C>T r.(?) p.(Arg15=)
?/. - c.70A>T r.(?) p.(Ile24Leu)
?/. - c.80A>G r.(?) p.(Gln27Arg)
-?/. - c.87T>C r.(?) p.(Ala29=)
-?/. - c.87T>C r.(?) p.(Ala29=)
?/. - c.115G>A r.(?) p.(Glu39Lys)
-?/. - c.132G>A r.(?) p.(Gln44=)
-?/. - c.141A>C r.(?) p.(Gln47His)
?/. - c.154C>T r.(?) p.(Arg52Trp)
-?/. - c.179G>A r.(?) p.(Cys60Tyr)
+?/. - c.212C>T r.(?) p.(Pro71Leu)
?/. - c.212C>T r.(?) p.(Pro71Leu)
?/. - c.268C>T r.(?) p.(Arg90Trp)
-?/. - c.268C>T r.(?) p.(Arg90Trp)
-/. - c.268C>T r.(?) p.(Arg90Trp)
-/. - c.268C>T r.(?) p.(Arg90Trp)
-?/. - c.271-24A>G r.(=) p.(=)
+?/. - c.280G>A r.(?) p.(Val94Met)
?/. - c.281T>G r.(?) p.(Val94Gly)
?/. - c.297G>T r.(?) p.(Arg99Ser)
-?/. - c.308G>A r.(?) p.(Arg103Gln)
-?/. - c.322C>T r.(?) p.(Arg108Trp)
?/. - c.364A>G r.(?) p.(Thr122Ala)
-?/. - c.365C>T r.(?) p.(Thr122Met)
-?/. - c.372C>T r.(?) p.(Ile124=)
?/. - c.374A>G r.(?) p.(Lys125Arg)
-?/. - c.390-9G>A r.(=) p.(=)
-/. - c.390-9G>A r.(=) p.(=)
-?/. - c.406A>G r.(?) p.(Ile136Val)
-?/. - c.458C>T r.(?) p.(Pro153Leu)
?/. - c.472T>G r.(?) p.(Tyr158Asp)
+?/. - c.472T>G r.(?) p.(Tyr158Asp)
?/. - c.476T>C r.(?) p.(Val159Ala)
?/. - c.483T>A r.(?) p.(Thr161=)
-?/. - c.503C>A r.(?) p.(Ala168Asp)
?/. - c.542A>C r.(?) p.(Glu181Ala)
-?/. - c.543G>A r.(?) p.(Glu181=)
-?/. - c.585C>T r.(?) p.(Ser195=)
?/. - c.599C>T r.(?) p.(Ala200Val)
-?/. - c.600-33T>G r.(=) p.(=)
-/. - c.618A>G r.(?) p.(Ile206Met)
-/. - c.618A>G r.(?) p.(Ile206Met)
?/. - c.626G>A r.(?) p.(Arg209His)
-?/. - c.630G>A r.(?) p.(Gly210=)
?/. - c.643C>T r.(?) p.(Arg215Trp)
-?/. - c.648A>C r.(?) p.(Thr216=)
-?/. - c.648A>C r.(?) p.(Thr216=)
-/. - c.648A>C r.(?) p.(Thr216=)
?/. - c.724T>A r.(?) p.(Ser242Thr)
+?/. - c.724T>A r.(?) p.(Ser242Thr)
?/. - c.724T>A r.(?) p.(Ser242Thr)
+?/. - c.800T>A r.(?) p.(Leu267His)
-?/. - c.852T>C r.(?) p.(Asn284=)
-?/. - c.853G>A r.(?) p.(Glu285Lys)
-?/. - c.853G>A r.(?) p.(Glu285Lys)
-?/. - c.853G>A r.(?) p.(Glu285Lys)
-?/. - c.853G>A r.(?) p.(Glu285Lys)
-?/. - c.866A>G r.(?) p.(Tyr289Cys)
?/. - c.883+1G>A r.(?) p.(?)
-/. - c.883+27_883+63del r.(=) p.(=)
-/. - c.884-13T>C r.(=) p.(=)
-/. - c.884-13T>C r.(=) p.(=)
-?/. - c.905G>A r.(?) p.(Arg302Gln)
-?/. - c.905G>A r.(?) p.(Arg302Gln)
-?/. - c.905G>A r.(?) p.(Arg302Gln)
-?/. - c.950+3G>A r.spl? p.?
-?/. - c.950+17T>C r.(=) p.(=)
-/. - c.950+17T>C r.(=) p.(=)
-?/. - c.950+17T>C r.(=) p.(=)
-?/. - c.950+28G>A r.(=) p.(=)
-/. - c.969T>C r.(?) p.(Tyr323=)
-?/. - c.969T>C r.(?) p.(Tyr323=)
+/. - c.1087C>T r.(?) p.(Gln363*)
-?/. - c.1092+13A>C r.(=) p.(=)
-?/. - c.1092+13A>G r.(=) p.(=)
-/. - c.1092+18C>T r.(=) p.(=)
-/. - c.1093-15C>T r.(=) p.(=)
-?/. - c.1093-7C>A r.(=) p.(=)
-?/. - c.1093-7C>A r.(=) p.(=)
-?/. - c.1093-7C>A r.(=) p.(=)
?/. - c.1128T>G r.(?) p.(Phe376Leu)
?/. - c.1138G>A r.(?) p.(Val380Ile)
?/. - c.1138G>A r.(?) p.(Val380Ile)
+?/. - c.1141A>G r.(?) p.(Ile381Val)
-?/. - c.1155T>A r.(?) p.(Ser385=)
-/. - c.1157T>G r.(?) p.(Phe386Cys)
-?/. - c.1162C>T r.(?) p.(=)
?/. - c.1163T>C r.(?) p.(Leu388Pro)
?/. - c.1192A>G r.(?) p.(Met398Val)
?/. - c.1196C>T r.(?) p.(Ala399Val)
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