Transcript #00001225 (NM_019842.3, KCNQ5 gene)

Transcript name transcript variant 1
Gene name KCNQ5 (potassium voltage-gated channel, KQT-like subfamily, member 5)
Chromosome 6
Transcript - NCBI ID NM_019842.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_062816.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:19:55 +02:00 (CEST)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.51G>A r.(?) p.(Trp17Ter)
?/. - c.62G>C r.(?) p.(Gly21Ala)
-?/. - c.76G>A r.(?) p.(Ala26Thr)
?/. - c.77_89del r.(?) p.(Ala26Glyfs*7)
?/. - c.83G>A r.(?) p.(Gly28Asp)
?/. - c.104G>A r.(?) p.(Gly35Asp)
-?/. - c.227G>T r.(?) p.(Arg76Met)
?/. - c.238C>T r.(?) p.(Arg80Trp)
-?/. - c.366C>T r.(?) p.(Pro122=)
./. - c.399-4566_*2910112del - -
-?/. - c.472A>G r.(?) p.(Ser158Gly)
+/. - c.532C>T r.(?) p.(Arg178*)
+/. - c.532C>T r.(?) p.(Arg178*)
?/. - c.616+3G>A r.spl? p.?
?/. - c.616+13159G>T r.(=) p.(=)
?/. - c.616+13159G>T r.(=) p.(=)
?/. - c.616+14028C>G r.(=) p.(=)
?/. - c.616+14028C>G r.(=) p.(=)
?/. - c.616+14251A>G r.(=) p.(=)
?/. - c.616+14251A>G r.(=) p.(=)
?/. - c.634G>A r.(?) p.(Ala212Thr)
?/. - c.867G>T r.(?) p.(Lys289Asn)
+/. - c.867G>T r.(?) p.(Lys289Asn)
?/. - c.909G>T r.(?) p.(Trp303Cys)
-?/. - c.972A>G r.(?) p.(Gly324=)
-?/. - c.972A>G r.(?) p.(Gly324=)
+/. - c.1105C>A r.(?) p.(Pro369Thr)
?/. - c.1135C>T r.(?) p.(Arg379Cys)
-?/. - c.1169T>C r.(?) p.(Ile390Thr)
?/. - c.1184C>T r.(?) p.(Pro395Leu)
-?/. - c.1248-3584C>T r.(=) p.(=)
?/. - c.1248-3576C>T r.(=) p.(=)
+/. - c.1270C>T r.(?) p.(Arg424*)
-?/. - c.1271G>A r.(?) p.(Arg424Gln)
+/. - c.1271G>A r.(?) p.(Arg424Gln)
?/. - c.1286G>T r.(?) p.(Ser429Ile)
-?/. - c.1377C>T r.(?) p.(Thr459=)
-?/. - c.1404C>T r.(?) p.(Asn468=)
-?/. - c.1503T>C r.(?) p.(Asp501=)
-?/. - c.1577+3T>C r.spl? p.?
+/. - c.1646T>C r.(?) p.(Val549Ala)
+/. - c.1646T>C r.(?) p.(Val549Ala)
?/. - c.1670A>G r.(?) p.(His557Arg)
+/. - c.1670A>G r.(?) p.(His557Arg)
-?/. - c.1689A>G r.(?) p.(Arg563=)
-?/. - c.1689A>G r.(?) p.(Arg563=)
?/. - c.1709G>A r.(?) p.(Arg570His)
+?/. - c.1796A>G r.(?) p.(Asp599Gly)
?/. - c.1813C>T r.(?) p.(Arg605Trp)
-?/. - c.1824G>A r.(?) p.(Lys608=)
?/. - c.1900G>A r.(?) p.(Gly634Ser)
-?/. - c.1969T>A r.(?) p.(Tyr657Asn)
?/. - c.1969T>A r.(?) p.(Tyr657Asn)
-?/. - c.2067G>A r.(?) p.(Gln689=)
-?/. - c.2110G>A r.(?) p.(Ala704Thr)
?/. - c.2368A>G r.(?) p.(Asn790Asp)
-?/. - c.2405G>A r.(?) p.(Arg802His)
-?/. - c.2405G>A r.(?) p.(Arg802His)
-?/. - c.2608T>C r.(?) p.(Phe870Leu)
?/. - c.2617G>A r.(?) p.(Asp873Asn)
+?/. - c.2725C>T r.(?) p.(Arg909*)
?/. - c.2777T>C r.(?) p.(Leu926Ser)
?/. 14 c.*2608G>A r.(?) p.(=)
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