Transcript #00010338 (NM_004975.2, KCNB1 gene)

Transcript name potassium voltage-gated channel, Shab-related subfamily, member 1
Gene name KCNB1 (potassium voltage-gated channel, Shab-related subfamily, member 1)
Chromosome 20
Transcript - NCBI ID NM_004975.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_004966.1
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

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.99C>A r.(?) p.(Val33=)
+?/. - c.128A>G r.(128a>g) p.(Glu43Gly)
?/. - c.325_327del r.(?) p.(Glu109del)
?/. - c.359A>T r.(?) p.(Asp120Val)
-?/. - c.375C>T r.(?) p.(Asp125=)
?/. - c.451G>A r.(?) p.(Glu151Lys)
-?/. - c.490G>C r.(?) p.(Asp164His)
?/. - c.554C>T r.(?) p.(Ser185Phe)
+?/. - c.587T>C r.(?) p.(Ile196Thr)
+/. - c.629C>T r.(?) p.(Thr210Met)
+?/. 2 c.629C>T r.(?) p.(Thr210Met)
+/. - c.629C>T r.(?) p.(Thr210Met)
?/. - c.698A>G r.(?) p.(Glu233Gly)
?/. - c.752C>T r.(?) p.(Ser251Leu)
?/. - c.899G>C r.(?) p.(Arg300Pro)
+?/. - c.916C>T r.(?) p.(Arg306Cys)
+/. - c.916C>T r.(?) p.(Arg306Cys)
+?/. - c.916C>T r.(?) p.(Arg306Cys)
+?/. - c.919A>C r.(?) p.(Ile307Leu)
+/. - c.934C>T r.(?) p.(Arg312Cys)
+/. - c.934C>T r.(?) p.(Arg312Cys)
+?/. - c.934C>T r.(?) p.(Arg312Cys)
+?/. - c.946G>A r.(?) p.(Gly316Ser)
+?/. - c.968C>T r.(?) p.(Thr323Ile)
?/. 2 c.995G>C r.(?) p.(Gly332Ala)
+?/. - c.1041C>G r.(?) p.(Ser347Arg)
+?/. - c.1053T>G r.(?) p.(Phe351Leu)
?/. - c.1054G>T r.(?) p.(Ala352Ser)
-?/. - c.1077C>T r.(?) p.(Thr359=)
+/. - c.1121C>T r.(?) p.(Thr374Ile)
+/. - c.1133T>C r.(?) p.(Val378Ala)
+/. - c.1135G>A r.(?) p.(Gly379Arg)
+?/. - c.1135G>A r.(?) p.(Gly379Arg)
+/. - c.1141G>A r.(?) p.(Gly381Arg)
+?/. - c.1193G>T r.(?) p.(Cys398Phe)
+/. - c.1222C>T r.(?) p.(Pro408Ser)
?/. - c.1237G>A r.(?) p.(Val413Ile)
?/. - c.1237G>C r.(?) p.(Val413Leu)
+?/. - c.1248C>G r.(?) p.(Phe416Leu)
-?/. - c.1296G>A r.(?) p.(Arg432=)
?/. - c.1300G>C r.(?) p.(Glu434Gln)
-?/. - c.1305T>C r.(?) p.(Ala435=)
+/. - c.1463G>A r.(?) p.(Trp488Ter)
?/. - c.1468T>C r.(?) p.(Trp490Arg)
./. - c.1576G>A r.(?) p.(Val526Ile)
./. - c.1576G>A r.(?) p.(Val526Ile)
-?/. - c.1576G>A r.(?) p.(Val526Ile)
-?/. - c.1576G>A r.(?) p.(Val526Ile)
./. - c.1576G>A r.(?) p.(Val526Ile)
./. - c.1576G>A r.(?) p.(Val526Ile)
+?/. - c.1579C>T r.(?) p.(Gln527*)
+?/. - c.1614_1626del r.(?) p.(Lys538AsnfsTer28)
?/. - c.1662C>A r.(?) p.(Ser554Arg)
./. - c.1723C>A r.(?) p.(Arg575Ser)
./. - c.1723C>A r.(?) p.(Arg575Ser)
-?/. - c.1734G>C r.(?) p.(Gly578=)
-?/. - c.1847C>G r.(?) p.(Thr616Ser)
?/. - c.1997C>T r.(?) p.(Pro666Leu)
?/. - c.2008C>T r.(?) p.(Arg670*)
?/. - c.2051T>C r.(?) p.Leu684Pro
-?/. - c.2092C>T r.(?) p.(Arg698Trp)
?/. - c.2105C>A r.(?) p.(Ala702Glu)
-?/. - c.2106G>A r.(?) p.(Ala702=)
-?/. - c.2115C>T r.(?) p.(Val705=)
-?/. - c.2152G>A r.(?) p.(Val718Met)
-?/. - c.2323C>A r.(?) p.(Pro775Thr)
?/. - c.2323C>T r.(?) p.(Pro775Ser)
?/. - c.2478T>A r.(?) p.(Ser826Arg)
-?/. - c.2570G>A r.(?) p.(Ser857Asn)
-/. - c.2570G>A r.(?) p.(Ser857Asn)
-?/. - c.*13855_*13856insTAC r.(=) p.(=)
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