Transcript #00000176 (NM_000123.2, ERCC5 gene)

Transcript name excision repair cross-complementing rodent repair deficiency, complementation group 5 (expired, new version available)
Gene name ERCC5 (excision repair cross-complementing rodent repair deficiency, complementation group 5)
Chromosome 13
Transcript - NCBI ID NM_000123.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000114.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-05-11 13:12:20 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.26T>C r.(?) p.(Leu9Pro)
+/. - c.50del r.(?) p.(Val17AlafsTer19)
?/. - c.56C>T r.(?) p.(Pro19Leu)
?/. - c.73A>G r.(?) p.(Lys25Glu)
-?/. - c.76A>G r.(?) p.(Ile26Val)
+/. 1 c.83C>A r.(?) p.(Ala28Asp)
+/. 1 c.83C>A r.(?) p.(Ala28Asp)
-?/. - c.134G>A r.(?) p.(Arg45His)
+/. - c.136del r.(?) p.(His46Metfs*5)
-/. - c.138T>C r.(?) p.(His46=)
-/. - c.138T>C r.(?) p.(His46=)
?/. - c.170C>T r.(?) p.(Thr57Ile)
+/. - c.264+1del r.spl p.?
+/. - c.264+1del r.spl p.?
-/. - c.264+7G>A r.(=) p.(=)
-?/. - c.330G>A r.(?) p.(Leu110=)
-?/. - c.378A>G r.(?) p.(Lys126=)
-?/. - c.413G>A r.(?) p.(Arg138Gln)
-/. - c.429C>G r.(?) p.(Leu143=)
-/. - c.429C>G r.(?) p.(Leu143=)
-?/. - c.542A>G r.(?) p.(His181Arg)
?/. - c.550C>G r.(?) p.(Gln184Glu)
-?/. - c.592C>A r.(?) p.(Pro198Thr)
-?/. - c.592C>G r.(?) p.(Pro198Ala)
?/. - c.592C>G r.(?) p.(Pro198Ala)
-?/. - c.593C>T r.(?) p.(Pro198Leu)
?/. - c.640C>T r.(?) p.(Arg214Cys)
-/. - c.640C>T r.(?) p.(Arg214Cys)
-/. - c.641G>A r.(?) p.(Arg214His)
-/. - c.672+533T>C r.(=) p.(=)
+/. - c.697_700del r.(?) p.(Gln233SerfsTer10)
-?/. - c.760A>G r.(?) p.(Met254Val)
-/. - c.760A>G r.(?) p.(Met254Val)
-/. - c.760A>G r.(?) p.(Met254Val)
-?/. - c.760A>G r.(?) p.(Met254Val)
-?/. - c.767A>G r.(?) p.(Gln256Arg)
-/. - c.767A>G r.(?) p.(Gln256Arg)
?/. - c.787C>T r.(?) p.(Arg263*)
-?/. - c.788G>A r.(?) p.(Arg263Gln)
+/. - c.869T>A r.(?) p.(Ile290Asn)
?/. - c.926C>T r.(?) p.(Pro309Leu)
?/. - c.932C>G r.(?) p.(Ser311Cys)
-?/. - c.945C>T r.(?) p.(His315=)
-?/. - c.945C>T r.(?) p.(His315=)
-?/. - c.960C>T r.(?) p.(Asp320=)
-/. - c.960C>T r.(?) p.(Asp320=)
-?/. - c.1109G>A r.(?) p.(Arg370His)
-?/. - c.1110T>A r.(?) p.(Arg370=)
-?/. - c.1110T>A r.(?) p.(Arg370=)
-?/. - c.1147A>G r.(?) p.(Ile383Val)
-?/. - c.1225G>A r.(?) p.(Val409Met)
-?/. - c.1259G>A r.(?) p.(Arg420His)
-?/. - c.1259G>A r.(?) p.(Arg420His)
-?/. - c.1287T>C r.(?) p.(Asp429=)
-?/. - c.1328C>G r.(?) p.(Thr443Ser)
-/. - c.1440C>T r.(?) p.(His480=)
-/. - c.1440C>T r.(?) p.(His480=)
-?/. - c.1499G>A r.(?) p.(Arg500Gln)
-?/. - c.1538C>G r.(?) p.(Ala513Gly)
-?/. - c.1557A>C r.(?) p.(Gly519=)
-/. - c.1586G>C r.(?) p.(Cys529Ser)
-/. - c.1586G>C r.(?) p.(Cys529Ser)
-/. - c.1586G>C r.(?) p.(Cys529Ser)
-?/. - c.1694A>G r.(?) p.(Asp565Gly)
-?/. - c.1738C>G r.(?) p.(Pro580Ala)
+/. - c.1753G>T r.(?) p.(Glu585*)
+/. - c.1753G>T r.(?) p.(Glu585*)
-?/. - c.1768G>A r.(?) p.(Val590Ile)
-?/. - c.1768G>A r.(?) p.(Val590Ile)
-?/. - c.1789G>C r.(?) p.(Val597Leu)
-?/. - c.1789G>C r.(?) p.(Val597Leu)
+/. - c.1842del r.(?) p.(Leu615Trpfs*17)
?/. - c.1880C>A r.(?) p.(Ala627Glu)
-?/. - c.1911C>T r.(?) p.(Ala637=)
-?/. - c.2042G>T r.(?) p.(Gly681Val)
-/. - c.2100C>A r.(?) p.(Leu700=)
-?/. - c.2108A>G r.(?) p.(Asp703Gly)
-?/. - c.2163G>A r.(?) p.(Ala721=)
-?/. - c.2199+14A>G r.(=) p.(=)
?/. - c.2281G>A r.(?) p.(Ala761Thr)
?/. - c.2281G>A r.(?) p.(Ala761Thr)
+?/. - c.2353C>T r.(?) p.(Gln785Ter)
+/. - c.2353C>T r.(?) p.(Gln785Ter)
-?/. - c.2382C>T r.(?) p.(Cys794=)
+/. - c.2383G>A r.(?) p.(Ala795Thr)
+/. - c.2413G>A r.(?) p.(Gly805Arg)
-?/. - c.2421C>T r.(?) p.(Ile807=)
+/. - c.2453C>T r.(?) p.(Ala818Val)
+/. - c.2453C>T r.(?) p.(Ala818Val)
+/. - c.2453C>T r.(?) p.(Ala818Val)
-?/. - c.2454G>A r.(?) p.(Ala818=)
-?/. - c.2534-10T>G r.(=) p.(=)
?/. - c.2542C>T r.(?) p.(Arg848Trp)
?/. - c.2542C>T r.(?) p.(Arg848Trp)
+/. - c.2586_2587del r.(?) p.(Thr863Argfs*17)
?/. - c.2636A>G r.(?) p.(Asn879Ser)
-/. - c.2636A>G r.(?) p.(Asn879Ser)
?/. - c.2636A>G r.(?) p.(Asn879Ser)
-/. - c.2768T>C r.(?) p.(Leu923Pro)
+/. - c.2775del r.(?) p.(Gly926AlafsTer56)
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