Transcript #00025332 (NM_004366.5, CLCN2 gene)

Transcript name transcript variant 1
Gene name CLCN2 (chloride channel, voltage-sensitive 2)
Chromosome 3
Transcript - NCBI ID NM_004366.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_004357.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-10-23 22:56:07 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.0 r.0 p.0
-?/. - c.17C>T r.(?) p.(Ala6Val)
-?/. - c.60C>T r.(?) p.(Thr20=)
-?/. - c.143C>G r.(?) p.(Pro48Arg)
-/. - c.143C>G r.(?) p.(Pro48Arg)
-?/. - c.143C>G r.(?) p.(Pro48Arg)
-?/. - c.197G>A r.(?) p.(Arg66Gln)
?/. - c.202C>T r.(?) p.(Arg68Cys)
-/. - c.203G>A r.(?) p.(Arg68His)
-?/. - c.203G>A r.(?) p.(Arg68His)
-/. - c.203G>A r.(?) p.(Arg68His)
-?/. - c.218G>A r.(?) p.(Arg73His)
?/. - c.218G>A r.(?) p.(Arg73His)
-?/. - c.218G>A r.(?) p.(Arg73His)
+?/. - c.221-2A>G r.spl? p.?
?/. 3 c.246C>G r.(?) p.(Phe82Leu)
?/. - c.370C>T r.(?) p.(Arg124Trp)
?/. - c.374G>A r.(?) p.(Gly125Asp)
-/. - c.481+12G>A r.(=) p.(=)
-?/. - c.567C>T r.(?) p.(Val189=)
-?/. - c.616-19C>T r.(=) p.(=)
-?/. - c.616-19C>T r.(=) p.(=)
?/. - c.634G>A r.(?) p.(Ala212Thr)
-?/. - c.673C>T r.(?) p.(Leu225Phe)
-?/. - c.673C>T r.(?) p.(Leu225Phe)
?/. - c.694A>G r.(?) p.(Asn232Asp)
?/. - c.704G>A r.(?) p.(Arg235Gln)
?/. - c.704G>A r.(?) p.(Arg235Gln)
-?/. - c.704G>A r.(?) p.(Arg235Gln)
?/. - c.704G>A r.(?) p.(Arg235Gln)
?/. - c.719T>C r.(?) p.(Leu240Pro)
?/. - c.719T>C r.(?) p.(Leu240Pro)
-?/. - c.738G>C r.(?) p.(=)
?/. - c.898+2T>G r.spl? p.?
-/. - c.906T>C r.(?) p.(Ile302=)
-/. - c.906T>C r.(?) p.(Ile302=)
-?/. - c.936C>G r.(?) p.(Leu312=)
?/. - c.937G>A r.(?) p.(Asp313Asn)
+/. - c.969del r.(?) p.(Phe324LeufsTer18)
?/. - c.989C>T r.(?) p.(Ala330Val)
?/. - c.992G>C r.(?) p.(Ser331Thr)
?/. - c.1026C>G r.(?) p.(Asn342Lys)
-?/. - c.1086-17G>A r.(=) p.(=)
-?/. - c.1101G>A r.(?) p.(Pro367=)
-/. - c.1101G>A r.(?) p.(Pro367=)
?/. - c.1214C>T r.(?) p.(Thr405Met)
?/. - c.1214C>T r.(?) p.(Thr405Met)
?/. - c.1214C>T r.(?) p.(Thr405Met)
?/. - c.1250C>G r.(?) p.(Pro417Arg)
-?/. - c.1326+14G>A r.(=) p.(=)
-?/. - c.1396+99C>A r.(=) p.(=)
-/. - c.1397-13C>T r.(=) p.(=)
-?/. - c.1397-11C>G r.(=) p.(=)
-?/. - c.1397-11C>G r.(=) p.(=)
-?/. - c.1416G>C r.(?) p.(Leu472=)
-?/. - c.1461G>T r.(?) p.(Thr487=)
?/. - c.1478G>A r.(?) p.(Arg493Gln)
?/. - c.1486C>T r.(?) p.(Pro496Ser)
-?/. - c.1507+16C>T r.(=) p.(=)
-?/. - c.1508-16G>A r.(=) p.(=)
?/. - c.1529C>T r.(?) p.(Ala510Val)
?/. - c.1529C>T r.(?) p.(Ala510Val)
-?/. - c.1530G>A r.(?) p.(Ala510=)
-?/. - c.1548C>A r.(?) p.(Ser516=)
-?/. - c.1548C>A r.(?) p.(Ser516=)
?/. - c.1550C>T r.(?) p.(Thr517Met)
-?/. - c.1560C>T r.(?) p.(Ile520=)
-?/. - c.1626C>T r.(?) p.(Asn542=)
-/. - c.1626C>T r.(?) p.(Asn542=)
?/. - c.1633G>A r.(?) p.(Ala545Thr)
?/. - c.1652C>A r.(?) p.(Ser551Tyr)
-?/. - c.1704C>T r.(?) p.(Leu568=)
+/. - c.1709G>A r.(?) p.(Trp570*)
-?/. - c.1721+5G>A r.spl? p.?
-?/. - c.1722-19C>T r.(=) p.(=)
-?/. - c.1722-18G>A r.(=) p.(=)
-?/. - c.1722-18G>A r.(=) p.(=)
?/. - c.1724A>T r.(?) p.(Gln575Leu)
?/. - c.1730G>A r.(?) p.(Arg577Gln)
?/. - c.1730G>A r.(?) p.(Arg577Gln)
?/. - c.1757G>A r.(?) p.(Arg586Gln)
?/. - c.1795G>A r.(?) p.(Asp599Asn)
?/. - c.1795G>A r.(?) p.(Asp599Asn)
?/. - c.1829G>A r.(?) p.(Arg610Gln)
-?/. - c.1856-3C>T r.spl? p.?
-?/. - c.1856-3C>T r.spl? p.?
?/. - c.1885C>T r.(?) p.(Arg629Cys)
-/. - c.1932_1934dup r.(?) p.(Arg646dup)
-?/. - c.1932_1934dup r.(?) p.(Arg646dup)
-/. - c.1932_1934dup r.(?) p.(Arg646dup)
-?/. - c.1937G>A r.(?) p.(Arg646Gln)
-?/. - c.1937G>A r.(?) p.(Arg646Gln)
-?/. - c.1937G>A r.(?) p.(Arg646Gln)
-?/. - c.1956C>T r.(?) p.(=)
+/. - c.1957A>T r.(?) p.(Arg653Ter)
-?/. - c.1981T>A r.(?) p.(Ser661Thr)
-?/. - c.1981T>A r.(?) p.(Ser661Thr)
-?/. - c.1991A>T r.(?) p.(Glu664Val)
-/. - c.2003C>G r.(?) p.(Thr668Ser)
-/. - c.2003C>G r.(?) p.(Thr668Ser)
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