Transcript #00005238 (NM_000085.4, CLCNKB gene)

Transcript name transcript variant 1
Gene name CLCNKB (chloride channel, voltage-sensitive Kb)
Chromosome 1
Transcript - NCBI ID NM_000085.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000076.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-152_410{0} r.0 p.0
+/. - c.-152_410{0} r.0 p.0
+/. - c.-152_410{0} r.0 p.0
+/. - c.-11640_230-185del r.0? p.0?
+/. - c.-152_576del r.? p.?
+/. - c.-152_*410del r.(?) p.0?
+/? 1_20 c.(?_-136)_(*392_?)del r.0 p.0
-/. - c.-69G>T r.(?) p.(=)
-/. - c.-7-108C>T r.(=) p.(=)
+/. - c.-152_(1227+64_?){0} r.0? p.0?
+/. - c.-152_(576+1_577-1)[0] r.0? p.0?
?/. - c.2T>A r.? p.(Met1Lys)
-?/. - c.45T>C r.(?) p.(Pro15=)
-/. - c.80G>T r.(?) p.(Arg27Leu)
-/. - c.80G>T r.(?) p.(Arg27Leu)
-/. - c.100+93C>T r.(=) p.(=)
-?/. - c.171G>A r.(?) p.(Gly57=)
-?/. - c.171G>A r.(?) p.(Gly57=)
?/. - c.172G>T r.(?) p.(Val58Leu)
-/. - c.229+102T>G r.(=) p.(=)
-/. - c.229+110G>A r.(=) p.(=)
-?/. - c.231G>A r.(?) p.(Ala77=)
+/? 4 c.242T>C r.(?) p.(Leu81Pro)
+/? 4 c.274C>T r.(?) p.(Arg92Trp)
-/. - c.310G>A r.(?) p.(Val104Ile)
-/. - c.324A>G r.(?) p.(Ser108=)
-/. - c.324A>G r.(?) p.(Ser108=)
+/. - c.343A>C r.(?) p.(Thr115Pro)
-/. - c.359-6G>C r.(=) p.(=)
+/. - c.371C>T r.(?) p.(Pro124Leu)
+?/? 5 c.446T>A r.(?) p.(Val149Glu)
+/. - c.446T>A r.(?) p.(Val149Glu)
-/. - c.492G>C r.(?) p.(Gly164=)
-/. - c.492G>C r.(?) p.(Gly164=)
+/. - c.498+1G>C r.spl? p.?
?/. - c.499G>A r.(?) p.(Gly167Ser)
+?/. 5 c.500G>T r.(?) p.(Gly167Val)
-?/. - c.510G>C r.(?) p.(Val170=)
-/. - c.577-5C>T r.spl? p.?
-/. - c.577-5C>T r.spl? p.?
-/. - c.641C>G r.(?) p.(Ala214Gly)
-/. - c.641C>G r.(?) p.(Ala214Gly)
-/. - c.642A>C r.(?) p.(Ala214=)
-/. - c.642A>C r.(?) p.(Ala214=)
?/. - c.647C>T r.(?) p.(Pro216Leu)
?/. - c.656-68G>A r.(=) p.(=)
+?/. - c.656-31del r.(=) p.(=)
?/. - c.656-31del r.(=) p.(=)
+/. - c.656-31del r.(?) p.(=)
-?/. - c.656-14A>T r.(=) p.(=)
+?/. - c.656-2A>G r.spl? p.?
+/. - c.664T>C r.(?) p.(Phe222Leu)
+?/. 8 c.725C>A r.(?) p.(Ala242Glu)
+/. 8 c.725C>A r.(?) p.(Ala242Glu)
+/. 8 c.725C>A r.(?) p.(Ala242Glu)
+/? 8 c.736G>C r.(?) p.(Gly246Arg)
-?/. - c.762G>A r.(?) p.(=)
+/. - c.782-2A>G r.spl? p.?
+?/. - c.782-2A>G r.spl? p.?
-/. - c.860C>T r.(?) p.(Ala287Val)
-/. - c.860C>T r.(?) p.(Ala287Val)
+?/. 9 c.865G>C r.(?) p.(Gly289Arg)
-/. - c.866+35A>T r.(=) p.(=)
-/. - c.876T>C r.(?) p.(Cys292=)
-/. - c.876T>C r.(?) p.(Cys292=)
-/. - c.876T>C r.(?) p.(Cys292=)
+?/. - c.889A>G r.(?) p.(Ser297Gly)
+/. - c.937_940dup r.(?) p.(Arg314LysfsTer2)
+?/. - c.968+1G>A r.spl? p.?
+/. - c.968+1G>A r.spl? p.?
+/. - c.968+1G>A r.spl? p.?
-?/. - c.968+9C>T r.(=) p.(=)
-?/. - c.1000G>C r.(?) p.(Val334Leu)
+/? 11 c.1052G>C r.(?) p.(Arg315Pro)
-/. - c.1053+13G>C r.(=) p.(=)
-/. - c.1053+13G>C r.(=) p.(=)
?/. - c.1071T>A r.(?) p.(His357Gln)
-?/. - c.1092C>T r.(?) p.(Asn364=)
-?/. - c.1092C>T r.(?) p.(Asn364=)
+/. - c.1166G>A r.(?) p.(Trp389*)
-/. - c.1183C>T r.(?) p.(Arg395Trp)
-?/. - c.1192A>G r.(?) p.(Ile398Val)
+/. - c.1214_1221del r.(?) p.(Phe405TyrfsTer43)
+/. - c.1227+2T>A r.spl? p.?
-/. - c.1227+61dup r.(=) p.(=)
-/. - c.1228-73A>G r.(=) p.(=)
+?/. - c.1234A>G r.(?) p.(Met412Val)
-/. - c.1254C>T r.(?) p.(Thr418=)
-/. - c.1255A>G r.(?) p.(Ile419Val)
+/? 13 c.1271G>A r.(?) p.(Gly424Glu)
+/? 13 c.1271G>A r.(?) p.(Gly424Glu)
-?/. - c.1297+5G>T r.spl? p.?
-/. - c.1297+5G>T r.spl? p.?
+/. - c.1298G>A r.(?) p.(Gly433Glu)
-/. - c.1308C>T r.(=) p.(=)
-/. - c.1308C>T r.(?) p.(Ile436=)
+/. - c.1312C>T r.(?) p.(Arg438Cys)
+/. - c.1312C>T r.(?) p.(Arg438Cys)
+/? 14 c.1313G>A r.(?) p.(Arg438His)
+/? 14 c.1316T>C r.(?) p.(Leu439Pro)
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