Transcript #00007207 (NM_000122.1, ERCC3 gene)

Transcript name excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)
Gene name ERCC3 (excision repair cross-complementing rodent repair deficiency, complementation group 3)
Chromosome 2
Transcript - NCBI ID NM_000122.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_000113.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.25C>G r.(?) p.(Arg9Gly)
-?/. - c.29-15G>T r.(=) p.(=)
?/. - c.36_38del r.(?) p.(Lys13del)
-?/. - c.126G>A r.(?) p.(Ala42=)
-?/. - c.144G>C r.(?) p.(Glu48Asp)
?/. - c.224C>T r.(?) p.(Pro75Leu)
-?/. - c.240C>T r.(?) p.(Pro80=)
+/. - c.296T>C r.(?) p.(Phe99Ser)
+/. - c.296T>C r.(?) p.(Phe99Ser)
+/. - c.325C>T r.(?) p.(Arg109Ter)
+/. - c.325C>T r.(?) p.(Arg109Ter)
+/. - c.325C>T r.(?) p.(Arg109*)
?/. - c.326G>A r.(?) p.(Arg109Gln)
?/. - c.362A>G r.(?) p.(Tyr121Cys)
-?/. - c.417C>T r.(?) p.(Tyr139=)
-?/. - c.417C>T r.(?) p.(Tyr139=)
-?/. - c.576C>T r.(?) p.(Pro192=)
+/. - c.576_583del r.(?) p.(Val193Argfs*8)
-?/. - c.611G>A r.(?) p.(Gly204Glu)
-/. - c.615G>A r.(?) p.(Glu205=)
-?/. - c.618C>T r.(?) p.(Ala206=)
-?/. - c.618C>T r.(?) p.(Ala206=)
-?/. - c.657C>T r.(?) p.(=)
+/. - c.760C>T r.(?) p.(Gln254Ter)
+/. - c.760C>T r.(?) p.(Gln254Ter)
-?/. - c.789_791del r.(?) p.(Glu264del)
?/. - c.789_791del r.(?) p.(Glu264del)
-?/. - c.801A>G r.(?) p.(Thr267=)
-?/. - c.822+14C>T r.(=) p.(=)
?/. - c.847C>T r.(?) p.(Arg283Cys)
-?/. - c.847C>T r.(?) p.(Arg283Cys)
?/. - c.847C>T r.(?) p.(Arg283Cys)
-?/. - c.847C>T r.(?) p.(Arg283Cys)
?/. - c.917T>C r.(?) p.(Ile306Thr)
-?/. - c.1005G>A r.(?) p.(Ser335=)
-?/. - c.1008G>A r.(?) p.(Gly336=)
-/. - c.1027+3A>G r.spl? p.?
-?/. - c.1028-16C>T r.(=) p.(=)
?/. - c.1055C>A r.(?) p.(Thr352Asn)
?/. - c.1078C>T r.(?) p.(Arg360Cys)
-?/. - c.1110T>C r.(?) p.(Ser370=)
-?/. - c.1119G>A r.(?) p.(Gln373=)
?/. - c.1153G>A r.(?) p.(Asp385Asn)
?/. - c.1270G>A r.(?) p.(Glu424Lys)
+/. - c.1273C>T r.(?) p.(Arg425*)
-?/. - c.1335C>T r.(?) p.(Thr445=)
-/. - c.1485G>A r.(?) p.(Glu495=)
-?/. - c.1485G>A r.(?) p.(Glu495=)
-?/. - c.1528-9G>A r.(=) p.(=)
+/. - c.1588C>T r.(?) p.(Arg530*)
+/. - c.1720C>T r.(?) p.(Arg574Ter)
?/. - c.1750A>G r.(?) p.(Thr584Ala)
+/. - c.1757del r.(?) p.(Gln586ArgfsTer25)
?/. - c.1757del r.(?) p.(Gln586ArgfsTer25)
+/. - c.1757del r.(?) p.(Gln586ArgfsTer25)
+/. - c.1757delA r.(?) p.(Gln586ArgfsTer25)
+/. - c.1762G>T r.(?) p.(Glu588*)
-?/. - c.1960G>A r.(?) p.(Glu654Lys)
-/. - c.1962G>C r.(?) p.(Glu654Asp)
-?/. - c.2080G>A r.(?) p.(Ala694Thr)
-?/. - c.2111C>T r.(?) p.(Ser704Leu)
?/. - c.2111C>T r.(?) p.(Ser704Leu)
?/. - c.2111C>T r.(?) p.(Ser704Leu)
-?/. - c.2112G>A r.(?) p.(Ser704=)
-?/. - c.2218-6C>T r.(=) p.(=)
-?/. - c.2268T>C r.(?) p.(Thr756=)
-?/. - c.2304G>A r.(?) p.(=)
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