Transcript #00024248 (NM_004980.4, KCND3 gene)

Transcript name transcript variant 1
Gene name KCND3 (potassium voltage-gated channel, Shal-related subfamily, member 3)
Chromosome 1
Transcript - NCBI ID NM_004980.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004971.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-04-22 16:07:10 +02:00 (CEST)
Date last edited N/A


Variants

97 entries on 1 page. Showing entries 1 - 97.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-210G>T r.(?) p.(=)
-?/. - c.5C>A r.(?) p.(Ala2Glu)
-?/. - c.5C>A r.(?) p.(Ala2Glu)
?/. - c.5C>A r.(?) p.(Ala2Glu)
-?/. - c.5C>A r.(?) p.(Ala2Glu)
-?/. - c.5C>A r.(?) p.(Ala2Glu)
-?/. - c.9C>T r.(?) p.(Ala3=)
?/. - c.43G>A r.(?) p.(Ala15Thr)
-?/. - c.96C>T r.(?) p.(Ala32=)
-/. - c.117T>C r.(?) p.(Asp39=)
-?/. - c.117T>C r.(?) p.(Asp39=)
-/. - c.264C>T r.(?) p.(Pro88=)
-/. - c.264C>T r.(?) p.(Pro88=)
-/. - c.321C>A r.(?) p.(Arg107=)
-?/. - c.321C>A r.(?) p.(Arg107=)
-?/. - c.348C>T r.(?) p.(Asp116=)
-/. - c.375G>A r.(?) p.(Pro125=)
-/. - c.375G>A r.(?) p.(Pro125=)
-/. - c.459G>A r.(?) p.(Ser153=)
?/. - c.500A>C r.(?) p.(Gln167Pro)
-/. - c.534C>T r.(?) p.(=)
?/. - c.611C>G r.(?) p.(Thr204Arg)
-/. - c.627G>C r.(?) p.(Thr209=)
-?/. - c.627G>C r.(?) p.(Thr209=)
-?/. - c.641A>G r.(?) p.(Lys214Arg)
-?/. - c.641A>G r.(?) p.(Lys214Arg)
-?/. - c.651G>A r.(?) p.(Pro217=)
-/. - c.651G>A r.(?) p.(Pro217=)
-/. - c.669G>C r.(?) p.(Ser223=)
-/. - c.669G>C r.(?) p.(Ser223=)
?/. - c.730C>T r.(?) p.(Arg244Trp)
?/. - c.787G>A r.(?) p.(Asp263Asn)
-/. - c.789C>T r.(?) p.(Asp263=)
-/. - c.870G>T r.(?) p.(Arg290=)
+/. - c.877_885dup r.(?) p.(Val294_Arg296dup)
+/. - c.880G>T r.(?) p.(Val294Phe)
+?/. - c.910T>C r.(?) p.(Ser304Pro)
+?/. - c.917G>T r.(?) p.(Gly306Val)
?/. - c.929T>C r.(?) p.(Leu310Pro)
-?/. - c.957C>G r.(?) p.(Ser319=)
-/. - c.957C>T r.(?) p.(Ser319=)
+?/. - c.958G>A r.(?) p.(Glu320Lys)
+?/. 2 c.1016T>C r.(?) p.(Met339Thr)
-/. - c.1026C>T r.(?) p.(Ala342=)
?/. - c.1058G>T r.(?) p.(Ser353Ile)
-?/. - c.1062C>A r.(?) p.(Ile354=)
-?/. - c.1062C>A r.(?) p.(Ile354=)
-/. - c.1062C>A r.(?) p.(Ile354=)
+/. - c.1070C>T r.(?) p.(Ser357Leu)
+?/. - c.1090A>G r.(?) p.(Thr364Ala)
+/. - c.1097C>T r.(?) p.(Thr366Ile)
?/. - c.1099A>G r.(?) p.(Thr367Ala)
-?/. - c.1106+10C>T r.(=) p.(=)
-?/. - c.1106+10C>T r.(=) p.(=)
-/. - c.1106+10C>T r.(=) p.(=)
-/. - c.1106+11G>A r.(=) p.(=)
+?/. - c.1119G>A r.(?) p.(Met373Ile)
+/. 3 c.1153T>C r.(?) p.(Ser385Pro)
-/. - c.1161C>T r.(?) p.(Cys387=)
+?/. - c.1163C>T r.(?) p.(Ser388Phe)
+?/. - c.1169G>A r.(?) p.(Ser390Asn)
-?/. - c.1173C>A r.(?) p.(=)
+?/. - c.1174G>A r.(?) p.(Val392Ile)
+?/. 3 c.1174G>A r.(?) p.(Val392Ile)
-/. - c.1269+14G>A r.(=) p.(=)
-/. - c.1269+15C>A r.(=) p.(=)
-/. - c.1269+15C>A r.(=) p.(=)
-?/. - c.1270-6T>C r.(=) p.(=)
?/. - c.1292G>A r.(?) p.(Arg431His)
-/. - c.1323C>T r.(?) p.(Tyr441=)
-/. - c.1323C>T r.(?) p.(Tyr441=)
?/. - c.1348C>T r.(?) p.(Leu450Phe)
?/. - c.1348C>T r.(?) p.(Leu450Phe)
-/. - c.1372-6dup r.(=) p.(=)
-?/. - c.1372-6dup r.(=) p.(=)
-?/. - c.1438C>T r.(?) p.(Leu480=)
?/. - c.1453A>G r.(?) p.(Lys485Glu)
-?/. - c.1456A>G r.(?) p.(Thr486Ala)
?/. - c.1456A>G r.(?) p.(Thr486Ala)
-?/. - c.1456A>G r.(?) p.(Thr486Ala)
-?/. - c.1456A>G r.(?) p.(Thr486Ala)
?/. - c.1502G>A r.(?) p.(Arg501Gln)
-/. - c.1512C>T r.(?) p.(Thr504=)
-/. - c.1519-4G>T r.spl? p.?
-/. - c.1519-4G>T r.spl? p.?
?/. - c.1525G>A r.(?) p.(Glu509Lys)
-?/. - c.1573A>G r.(?) p.(Met525Val)
-?/. 7 c.1588T>C r.(?) p.(Ser530Pro)
?/. - c.1622G>A r.(?) p.(Gly541Asp)
?/. - c.1630A>G r.(?) p.(Thr544Ala)
+?/. - c.1649G>A r.(?) p.(Arg550His)
?/. - c.1736A>G r.(?) p.(Gln579Arg)
?/. - c.1798G>A r.(?) p.(Gly600Arg)
?/. - c.1798G>A r.(?) p.(Gly600Arg)
+?/. 8 c.1798G>A r.(?) p.(Gly600Arg)
-?/. - c.1937C>T r.(?) p.(Ala646Val)
-/. - c.1959C>T r.(?) p.(Ser653=)
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