Transcript #00000177 (NM_000124.2, ERCC6 gene)

Transcript name excision repair cross-complementing rodent repair deficiency, complementation group 6
Gene name ERCC6 (excision repair cross-complementing rodent repair deficiency, complementation group 6)
Chromosome 10
Transcript - NCBI ID NM_000124.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000115.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:12:20 +02:00 (CEST)
Date last edited N/A


Variants

214 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-154_*2370{0} r.0 p.0
-/. - c.-87C>A r.(?) p.(=)
-/. - c.-78G>T r.(?) p.(=)
-/. - c.135C>G r.(?) p.(Leu45=)
-/. - c.135C>G r.(?) p.(Leu45=)
-/. - c.135C>G r.(?) p.(Leu45=)
?/. - c.147T>C r.(?) p.(Ser49=)
-?/. - c.150G>A r.(?) p.(Val50=)
?/. - c.150G>A r.(?) p.(Val50=)
-?/. - c.384C>T r.(?) p.(Asp128=)
-/. - c.385G>A r.(?) p.(Val129Met)
-?/. - c.385G>A r.(?) p.(Val129Met)
-/. - c.411G>A r.(?) p.(Leu137=)
-/. - c.411G>A r.(?) p.(Leu137=)
+/. - c.526C>T r.(?) p.(Arg176*)
-?/. - c.528A>G r.(?) p.(Arg176=)
-/. - c.528A>G r.(?) p.(Arg176=)
+/. - c.550C>T r.(?) p.(Gln184*)
?/. - c.565A>G r.(?) p.(Thr189Ala)
+?/. - c.574C>T r.(?) p.(Gln192*)
+?/. - c.643G>T r.(?) p.(Glu215Ter)
?/. - c.646G>A r.(?) p.(Asp216Asn)
?/. - c.721C>T r.(?) p.(Arg241Cys)
?/. - c.802G>A r.(?) p.(Ala268Thr)
+/. - c.809del r.(?) p.(Gly270AlafsTer59)
?/. - c.979C>T r.(?) p.(Arg327Cys)
-?/. - c.986A>G r.(?) p.(Lys329Arg)
+/. 5 c.1012del r.(?) p.(Arg338GlyfsTer22)
-?/. - c.1044G>A r.(?) p.(Leu348=)
+/. - c.1135G>T r.(?) p.(Glu379Ter)
?/. - c.1145A>G r.(?) p.(Glu382Gly)
-/. - c.1146G>A r.(?) p.(Glu382=)
-?/. - c.1146G>A r.(?) p.(Glu382=)
-?/. - c.1158C>G r.(?) p.(Asp386Glu)
-?/. - c.1158C>G r.(?) p.(Asp386Glu)
-?/. - c.1158C>G r.(?) p.(Asp386Glu)
?/. - c.1159G>A r.(?) p.(Glu387Lys)
?/. - c.1159G>A r.(?) p.(Glu387Lys)
-?/. - c.1170G>A r.(?) p.(Gly390=)
-/. - c.1196G>A r.(?) p.(Gly399Asp)
-/. - c.1196G>A r.(?) p.(Gly399Asp)
-?/. - c.1241A>C r.(?) p.(Gln414Pro)
?/. - c.1274A>C r.(?) p.(Asp425Ala)
?/. - c.1274A>C r.(?) p.(Asp425Ala)
-?/. - c.1337G>A r.(?) p.(Gly446Asp)
-?/. - c.1337G>A r.(?) p.(Gly446Asp)
-?/. - c.1337G>A r.(?) p.(Gly446Asp)
-?/. - c.1337G>A r.(?) p.(Gly446Asp)
?/. - c.1339C>T r.(?) p.(Arg447Trp)
?/. - c.1339C>T r.(?) p.(Arg447Trp)
?/. - c.1378T>G r.(?) p.(Tyr460Asp)
?/. - c.1379A>C r.(?) p.(Tyr460Ser)
?/. - c.1397+7070_1397+7073del r.(=) p.(=)
-?/. - c.1397+7197G>A r.(=) p.(=)
?/. - c.1397+7318G>A r.(=) p.(=)
-?/. - c.1397+7359A>G r.(=) p.(=)
?/. - c.1397+7450T>C r.(=) p.(=)
?/. - c.1397+7541T>G r.(=) p.(=)
?/. - c.1397+7657C>T r.(=) p.(=)
-?/. - c.1397+7671C>T r.(=) p.(=)
?/. - c.1397+7750G>T r.(=) p.(=)
?/. - c.1397+7763G>A r.(=) p.(=)
?/. - c.1397+7904C>T r.(=) p.(=)
-/. - c.1397+8063G>A r.(=) p.(=)
-?/. - c.1397+8066T>C r.(=) p.(=)
-/. - c.1397+8395C>T r.(=) p.(=)
-?/. - c.1435C>T r.(?) p.(Arg479Cys)
-?/. - c.1436G>A r.(?) p.(Arg479His)
-?/. - c.1445T>G r.(?) p.(Leu482Arg)
?/. - c.1457C>G r.(?) p.(Ser486Cys)
+/. - c.1526+1G>T r.spl? p.?
+/. 7 c.1536dup r.(?) p.(Thr513AspfsTer4)
-?/. - c.1650C>T r.(?) p.(Ser550=)
?/. - c.1652_1653insT r.(?) p.(Ser552Glnfs*13)
?/. - c.1659G>T r.(?) p.(Lys553Asn)
-?/. - c.1659G>T r.(?) p.(Lys553Asn)
?/. - c.1669C>G r.(?) p.(Arg557Gly)
?/. - c.1669C>T r.(?) p.(Arg557Cys)
?/. - c.1670G>A r.(?) p.(Arg557His)
?/. - c.1772C>T r.(?) p.(Pro591Leu)
?/. - c.1772C>T r.(?) p.(Pro591Leu)
?/. - c.1801G>A r.(?) p.(Gly601Ser)
?/. - c.1801G>A r.(?) p.(Gly601Ser)
-/. - c.1821+7C>T r.(=) p.(=)
-/. - c.1821+7C>T r.(=) p.(=)
-/. - c.1821+7C>T r.(=) p.(=)
./. - c.1945C>T r.(?) p.(His649Tyr)
./. - c.1945C>T r.(?) p.(His649Tyr)
?/. - c.1946A>G r.(?) p.(His649Arg)
+/. - c.1954C>T r.(?) p.(Arg652Ter)
-?/. - c.1992+7C>T r.(=) p.(=)
-?/. - c.1992+7C>T r.(=) p.(=)
?/. - c.1996C>T r.(?) p.(Arg666Cys)
?/. - c.1996C>T r.(?) p.(Arg666Cys)
?/. - c.1996C>T r.(?) p.(Arg666Cys)
+/. - c.2008C>T r.(?) p.(Arg670Trp)
?/. - c.2053C>G r.(?) p.(Leu685Val)
-/. - c.2082G>A r.(?) p.(Pro694=)
?/. - c.2096C>T r.(?) p.(Thr699Met)
?/. - c.2167C>A r.(?) p.(Gln723Lys)
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