Transcript #00000314 (NM_004519.3, KCNQ3 gene)

Transcript name transcript variant 1
Gene name KCNQ3 (potassium voltage-gated channel, KQT-like subfamily, member 3)
Chromosome 8
Transcript - NCBI ID NM_004519.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004510.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 12:06:06 +02:00 (CEST)
Date last edited N/A


Variants

128 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.31dup r.(?) p.(Ala11Glyfs*17)
?/. - c.50_58dup r.(?) p.(Asp17_Gly19dup)
?/. - c.91G>A r.(?) p.(Gly31Arg)
?/. - c.105_107dup r.(?) p.(Ala36dup)
?/. - c.160A>G r.(?) p.(Thr54Ala)
?/. - c.170T>C r.(?) p.(Leu57Pro)
?/. - c.170T>C r.(?) p.(Leu57Pro)
-?/. - c.213C>T r.(?) p.(Gly71=)
?/. - c.220C>T r.(?) p.(Arg74Cys)
-/. - c.386+33162C>T r.(=) p.(=)
-/. - c.386+33167C>G r.(=) p.(=)
-/. - c.386+33167C>T r.(=) p.(=)
-/. - c.387-1129G>A r.(=) p.(=)
-/. - c.387-428C>T r.(=) p.(=)
-?/. - c.478-72G>T r.(=) p.(=)
?/. - c.604+1708G>A r.(=) p.(=)
-/. - c.660T>C r.(?) p.(Asn220=)
-/. - c.660T>C r.(?) p.(Asn220=)
-/. - c.660T>C r.(=) p.(=)
+/. - c.679C>T r.(?) p.(Arg227*)
?/. - c.680G>A r.(?) p.(Arg227Gln)
+?/. - c.688C>A r.(?) p.(Arg230Ser)
+/. - c.688C>A r.(?) p.(Arg230Ser)
+?/. - c.688C>T r.(?) p.(Arg230Cys)
+/. - c.689G>A r.(?) p.(Arg230His)
+/. - c.689G>A r.(?) p.(Arg230His)
+?/. - c.707G>A r.(?) p.(Arg236His)
-/. - c.732T>C r.(?) p.(Gly244=)
-/. - c.732T>C r.(?) p.(Gly244=)
-/. - c.732T>C r.(=) p.(=)
+?/. - c.767C>A r.(?) p.(Ala256Asp)
-/. - c.777+135A>G r.(=) p.(=)
-?/. - c.834T>C r.(?) p.(Leu278=)
-/. - c.834T>C r.(?) p.(Leu278=)
?/. - c.856G>A r.(?) p.(Val286Ile)
?/. - c.856G>A r.(?) p.(Val286Ile)
-/. - c.933+25T>C r.(=) p.(=)
-/. - c.933+25T>C r.(=) p.(=)
-/. - c.934-108G>A r.(=) p.(=)
?/. - c.950T>C r.(?) p.(Ile317Thr)
+/+ 6 c.950T>C r.(?) p.(Ile317Thr)
-?/. - c.977C>T r.(?) p.(Thr326Met)
+/. - c.988C>T r.(?) p.(Arg330Cys)
+/. - c.988C>T r.(?) p.(Arg330Cys)
+/. - c.988C>T r.(?) p.(Arg330Cys)
+?/. - c.988C>T r.(?) p.(Arg330Cys)
+?/. - c.989G>A r.(?) p.(Arg330His)
./. - c.1000G>A r.(?) p.(Ala334Thr)
?/. - c.1013T>C r.(?) p.(Leu338Ser)
?/. - c.1019G>T r.(?) p.(Gly340Val)
?/. - c.1044G>A r.(?) p.(=)
-/. - c.1044+156A>G r.(=) p.(=)
-/. - c.1044+195A>G r.(=) p.(=)
?/. - c.1048A>C r.(?) p.(Ile350Leu)
-/. - c.1071C>G r.(?) p.(Leu357=)
-/. - c.1071C>G r.(=) p.(=)
?/. - c.1114A>T r.(?) p.(Arg372Trp)
?/. - c.1121C>T r.(?) p.(Pro374Leu)
-/. - c.1140+77T>A r.(=) p.(=)
-?/. - c.1140+77T>A r.(=) p.(=)
-/. - c.1140+167G>C r.(=) p.(=)
./. - c.1142C>T r.(?) p.(Ala381Val)
-/. - c.1235+21A>G r.(=) p.(=)
-/. - c.1236-64C>T r.(=) p.(=)
-?/. - c.1236-16C>T r.(=) p.(=)
-/. - c.1241A>G r.(?) p.(Glu414Gly)
?/. - c.1249G>A r.(?) p.(Glu417Lys)
-?/. - c.1249_1250delinsAT r.(?) p.(Glu417Met)
?/. - c.1250A>T r.(?) p.(Glu417Val)
-?/. - c.1391T>C r.(?) p.(Val464Ala)
-?/. - c.1391T>C r.(?) p.(Val464Ala)
+/. - c.1403A>G r.(?) p.(Asn468Ser)
?/. - c.1403A>G r.(?) p.(Asn468Ser)
?/. - c.1457G>A r.(?) p.(Ser486Asn)
./. - c.1507G>A r.(?) p.(Gly503Arg)
?/. - c.1568+16T>C r.(=) p.(=)
-?/. - c.1583G>A r.(?) p.(Arg528His)
+?/. - c.1657G>A r.(?) p.(Gly553Arg)
?/. - c.1663C>T r.(?) p.(Leu555Phe)
-?/. - c.1700+3G>A r.spl? p.?
-/. - c.1700+29G>A r.(=) p.(=)
-/. - c.1700+29G>A r.(=) p.(=)
-/. - c.1701-148C>T r.(=) p.(=)
-/. - c.1701-143T>A r.(=) p.(=)
-/. - c.1701-141C>T r.(=) p.(=)
-/. - c.1701-133_1701-129del r.(=) p.(=)
-?/. - c.1701-126del r.(=) p.(=)
-/. - c.1701-126_1701-124del r.(=) p.(=)
?/. - c.1706A>G r.(?) p.(Asp569Gly)
?/. - c.1706A>G r.(?) p.(Asp569Gly)
?/. - c.1708_1709dup r.(?) p.(Met570Ilefs*2)
?/. - c.1709T>C r.(?) p.(Met570Thr)
./. - c.1709T>C r.(?) p.(Met570Thr)
-?/. - c.1720C>T r.(?) p.(Pro574Ser)
-?/. - c.1720C>T r.(?) p.(Pro574Ser)
-?/. - c.1720C>T r.(?) p.(Pro574Ser)
?/. - c.1720C>T r.(?) p.(Pro574Ser)
./. - c.1868T>C r.(?) p.(Val623Ala)
-/. - c.1884+12C>T r.(=) p.(=)
-/. - c.1884+80dup r.(=) p.(=)
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