Transcript #00018515 (NM_006920.4, SCN1A gene)

Transcript name transcript variant 2
Gene name SCN1A (sodium channel, voltage-gated, type I, alpha subunit)
Chromosome 2
Transcript - NCBI ID NM_006920.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_008851.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

554 entries on 6 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     
./. - c.-178423_*1269334del r.0? p.0? -
+?/. - c.(?_-112190)_(-4848_?)del r.0? p.0? -
+?/. _1 c.(?_-108889)_(-16994_?)del r.0? p.0? -
-?/. - c.-71506G>A r.(?) p.(=) -
-?/. - c.-61C>A r.(?) p.(=) -
?/. - c.25C>T r.(?) p.(Pro9Ser) -
?/. - c.32C>A r.(?) p.(Pro11His) -
?/. - c.32C>A r.(?) p.(Pro11His) -
-?/. - c.32C>A r.(?) p.(Pro11His) -
?/. - c.32C>A r.(?) p.(Pro11His) -
-?/. - c.32C>A r.(?) p.(Pro11His) -
?/. - c.65T>C r.(?) p.(Leu22Pro) -
+?/. - c.65T>C r.(?) p.(Leu22Pro) -
-?/. - c.68C>T r.(?) p.(Ala23Val) -
-?/. - c.68C>T r.(?) p.(Ala23Val) -
-?/. - c.80G>C r.(?) p.(Arg27Thr) -
+/. - c.82C>T r.(?) p.(Arg28Cys) -
?/. - c.83G>A r.(?) p.(Arg28His) -
+/. - c.133G>A r.(?) p.(Asp45Asn) -
+?/? 1 c.172G>A r.(?) p.(Gly58Arg) -
?/. - c.179A>G r.(?) p.(Asn60Ser) -
?/. - c.193T>C r.(?) p.(Tyr65His) -
?/. - c.230T>G r.(?) p.(Leu77Arg) -
+/. - c.268T>C r.(?) p.(Phe90Leu) -
?/. - c.286G>C r.(?) p.(Gly96Arg) -
+/. - c.301C>T r.(?) p.(Arg101Trp) -
?/. - c.302G>T r.(?) p.(Arg101Leu) -
-/. - c.345T>C r.(?) p.(Asn115=) -
-/. - c.345T>C r.(?) p.(Asn115=) -
-/. - c.345T>C r.(?) p.(Asn115=) -
+/. - c.352A>G r.(?) p.(Arg118Gly) -
+?/. - c.365T>C r.(?) p.(Ile122Thr) -
?/. - c.379C>G r.(?) p.(His127Asp) -
?/. - c.379C>G r.(?) p.(His127Asp) -
?/. - c.379C>G r.(?) p.(His127Asp) -
-/. - c.384-20G>C r.(=) p.(=) -
-/. - c.384-20G>C r.(=) p.(=) -
-?/. - c.384-19T>C r.(=) p.(=) -
+/. - c.384-1C>G r.spl? p.? -
+?/. - c.413T>C r.(?) p.(Ile138Thr) -
+?/. - c.419C>G r.(?) p.(Thr140Arg) -
?/. - c.421A>T r.(?) p.(Asn141Tyr) -
?/. - c.468T>G r.(?) p.(Asn156Lys) -
-/. - c.471A>G r.(?) p.(Val157=) -
-?/. - c.474-113T>C r.(=) p.(=) -
-?/. - c.474-32_474-23del r.(=) p.(=) -
+?/. - c.487G>A r.(?) p.(Gly163Arg) -
+/. - c.493T>C r.(?) p.(Tyr165His) -
-?/. - c.495T>C r.(?) p.(Tyr165=) -
-?/. - c.495T>C r.(?) p.(Tyr165=) -
?/. - c.524C>G r.(?) p.(Ala175Gly) -
+?/. - c.535T>A r.(?) p.(Cys179Ser) -
+?/. - c.547T>C r.(?) p.(Phe183Leu) -
+?/. - c.548T>C r.(?) p.(Phe183Ser) -
+?/. - c.560G>C r.(?) p.(Arg187Pro) -
+?/. - c.580G>C r.(?) p.(Asp194His) -
+?/. - c.602C>T r.(?) p.(Ala201Val) -
+/. - c.602+1G>C r.spl? p.? -
-?/. - c.602+6_602+7dup r.(=) p.(=) -
-?/. - c.602+6_602+7dup r.(=) p.(=) -
-?/. - c.603-143G>A r.(=) p.(=) -
-?/. - c.603-107C>T r.(=) p.(=) -
+/. - c.608T>A r.(?) p.(Val203Asp) -
+?/. - c.631A>G r.(?) p.(Asn211Asp) -
?/. - c.650C>T r.(?) p.(Thr217Ile) -
+/. - c.664C>T r.(?) p.(Arg222Ter) -
+/. - c.664C>T r.(?) p.(Arg222*) -
+/. - c.664C>T r.(?) p.(Arg222Ter) -
+?/. - c.664C>T r.(?) p.(Arg222*) -
?/. - c.665G>A r.(?) p.(Arg222Gln) -
+/. - c.677C>T r.(?) p.(Thr226Met) -
+/. - c.677C>T r.(?) p.(Thr226Met) -
+/. - c.677C>T r.(?) p.(Thr226Met) -
-?/. - c.678G>A r.(?) p.(Thr226=) -
-?/. - c.688A>G r.(?) p.(Ile230Val) -
+?/. - c.694+5G>C r.spl? p.? -
-?/. - c.694+10A>G r.(=) p.(=) -
-?/. - c.694+10A>G r.(=) p.(=) -
-?/. - c.694+10A>G r.(=) p.(=) -
-?/. - c.694+184G>A r.(=) p.(=) -
-/. - c.694+227T>G r.(=) p.(=) -
-/. - c.694+232_694+233insA r.(=) p.(=) -
-/. - c.694+233T>A r.(=) p.(=) -
?/. - c.695-10_695-3del r.(?) p.? -
-?/. - c.695-4del r.spl? p.? -
+/. - c.707T>C r.(?) p.(Ile236Thr) -
+/. - c.760A>C r.(?) p.(Thr254Pro) -
+/. - c.775A>C r.(?) p.(Ser259Arg) -
+/. - c.777C>A r.(?) p.(Ser259Arg) -
+/. - c.812G>A r.(?) p.(Gly271Asp) -
?/. - c.812G>A r.(?) p.(Gly271Asp) -
?/. - c.905G>T r.(?) p.(Gly302Val) -
-?/. - c.964+41T>A r.(=) p.(=) -
-?/. - c.964+104_964+110del r.(=) p.(=) -
-/. - c.965-21C>T r.(=) p.(=) -
+?/. - c.971A>C r.(?) p.(His324Pro) -
?/. - c.971A>G r.(?) p.(His324Arg) -
+?/. - c.995A>G r.(?) p.(Asp332Gly) -
+/. - c.1006T>G r.(?) p.(Cys336Gly) -
?/. - c.1009G>C r.(?) p.(Gly337Arg) -
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