Transcript #00007206 (NM_000400.3, ERCC2 gene)

Transcript name transcript variant 1
Gene name ERCC2 (excision repair cross-complementing rodent repair deficiency, complementation group 2)
Chromosome 19
Transcript - NCBI ID NM_000400.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000391.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.1A>G r.(?) p.?
?/. - c.2T>C r.(?) p.?
?/. - c.47A>G r.(?) p.(Tyr16Cys)
?/. - c.47A>G r.(?) p.(Tyr16Cys)
-?/. - c.57C>T r.(?) p.(Pro19=)
?/. - c.76C>G r.(?) p.(Arg26Gly)
?/. - c.85A>G r.(?) p.(Lys29Glu)
?/. - c.92C>T r.(?) p.(Thr31Met)
-?/. - c.177C>T r.(?) p.(Tyr59=)
./. - c.230_231del r.(?) p.(Val77Alafs*4)
?/. - c.260T>C r.(?) p.(Leu87Pro)
?/. - c.260T>C r.(?) p.(Leu87Pro)
?/. - c.260T>C r.(?) p.(Leu87Pro)
-/. - c.284A>G r.(?) p.(Glu95Gly)
-/. - c.284A>G r.(?) p.(Glu95Gly)
-?/. - c.284A>G r.(?) p.(Glu95Gly)
-?/. - c.292G>A r.(?) p.(Glu98Lys)
-?/. - c.294G>C r.(?) p.(Glu98Asp)
+?/. - c.334C>T r.(?) p.(Arg112Cys)
?/. - c.373C>T r.(?) p.(Arg125Cys)
-?/. - c.417C>G r.(?) p.(Ala139=)
?/. - c.428G>A r.(?) p.(Arg143Gln)
?/. - c.442C>T r.(?) p.(His148Tyr)
+/. - c.466C>T r.(?) p.(Arg156Ter)
-/. - c.468A>C r.(?) p.(Arg156=)
-/. - c.468A>C r.(?) p.(Arg156=)
?/. - c.473A>G r.(?) p.(Tyr158Cys)
-/. - c.477+9A>C r.(=) p.(=)
-/. - c.477+9A>C r.(=) p.(=)
-?/. - c.478-7G>T r.(=) p.(=)
-?/. - c.491A>G r.(?) p.(His164Arg)
?/. - c.496C>T r.(?) p.(Arg166Cys)
-?/. - c.545C>T r.(?) p.(Ala182Val)
?/. - c.556C>T r.(?) p.(Arg186Cys)
+/. - c.594+2_594+5del r.spl p.?
-?/. - c.595-11C>T r.(=) p.(=)
-?/. - c.595-8C>A r.(=) p.(=)
-?/. - c.601C>T r.(?) p.(His201Tyr)
-?/. - c.601C>T r.(?) p.(His201Tyr)
?/. - c.601C>T r.(?) p.(His201Tyr)
?/. - c.679C>T r.(?) p.(Arg227Cys)
?/. - c.679C>T r.(?) p.(Arg227Cys)
-?/. - c.687C>T r.(?) p.(Ala229=)
-?/. - c.687C>T r.(?) p.(Ala229=)
-/. - c.687C>T r.(?) p.(Ala229=)
?/. - c.691G>A r.(?) p.(Val231Met)
-?/. - c.699C>T r.(?) p.(Phe233=)
-?/. - c.699C>T r.(?) p.(Phe233=)
+/. - c.718+1G>T r.spl p.?
-/. - c.718+6G>T r.(=) p.(=)
-/. - c.718+6G>T r.(=) p.(=)
?/. - c.720C>G r.(?) p.(Asp240Glu)
?/. - c.720C>G r.(?) p.(Asp240Glu)
?/. - c.733G>A r.(?) p.(Asp245Asn)
?/. - c.733G>A r.(?) p.(Asp245Asn)
?/. - c.733G>A r.(?) p.(Asp245Asn)
?/. - c.776G>T r.(?) p.(Cys259Phe)
+/. - c.816-2A>G r.spl p.?
+/. - c.816-2A>G r.spl p.?
?/. - c.818T>G r.(?) p.(Ile273Ser)
-?/. - c.846G>A r.(?) p.(Arg282=)
?/. - c.884C>T r.(?) p.(Ala295Val)
-/. - c.934G>A r.(?) p.(Asp312Asn)
-/. - c.934G>A r.(?) p.(Asp312Asn)
-?/. - c.946C>G r.(?) p.(Gln316Glu)
-?/. - c.949+21G>A r.(=) p.(=)
-/. - c.949+27dup r.(=) p.(=)
-?/. - c.974C>T r.(?) p.(Thr325Met)
?/. - c.974C>T r.(?) p.(Thr325Met)
?/. - c.980A>T r.(?) p.(Glu327Val)
?/. - c.1003C>T r.(?) p.(Arg335Trp)
+/. - c.1017C>G r.(?) p.(Tyr339Ter)
?/. - c.1018G>A r.(?) p.(Val340Met)
?/. - c.1085C>T r.(?) p.(Ala362Val)
-?/. - c.1118+17C>T r.(=) p.(=)
-?/. - c.1119-5G>A r.spl? p.?
-?/. - c.1119-5G>A r.spl? p.?
+?/. - c.1132C>T r.(?) p.(Arg378Cys)
-?/. - c.1238-1207C>T r.(=) p.(=)
-?/. - c.1238-1191C>T r.(=) p.(=)
?/. - c.1238-1181C>T r.(=) p.(=)
?/. - c.1238-1175dup r.(=) p.(=)
?/. - c.1255G>A r.(?) p.(Glu419Lys)
-?/. - c.1267G>A r.(?) p.(Asp423Asn)
-?/. - c.1267G>A r.(?) p.(Asp423Asn)
?/. - c.1276C>G r.(?) p.(Pro426Ala)
?/. - c.1318G>A r.(?) p.(Ala440Thr)
?/. - c.1349G>A r.(?) p.(Arg450His)
?/. - c.1349G>A r.(?) p.(Arg450His)
?/. - c.1376G>A r.(?) p.(Gly459Glu)
-/. - c.1377+8C>T r.(=) p.(=)
-?/. - c.1377+16C>T r.(=) p.(=)
+/. - c.1378-26_1383del r.spl p.?
-/. - c.1378-23T>C r.(=) p.(=)
-?/. - c.1378-8C>T r.(=) p.(=)
-?/. - c.1378-7G>A r.(=) p.(=)
?/. - c.1381C>G r.(?) p.(Leu461Val)
?/. - c.1381C>G r.(?) p.(Leu461Val)
?/. - c.1381C>G r.(?) p.(Leu461Val)
+/. - c.1381C>G r.(?) p.(Leu461Val)
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