Transcript #00001805 (NM_000096.3, CP gene)

Transcript name transcript variant 1
Gene name CP (ceruloplasmin (ferroxidase))
Chromosome 3
Transcript - NCBI ID NM_000096.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000087.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2013-04-24 12:33:55 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.6G>A r.(?) p.(Lys2=)
?/. - c.70T>C r.(?) p.(Tyr24His)
-?/. - c.93G>A r.(?) p.(Thr31=)
-?/. - c.146C>T r.(?) p.(Thr49Met)
+?/. - c.164A>G r.(?) p.(Tyr55Cys)
?/. - c.188T>C r.(?) p.(Ile63Thr)
-?/. - c.247A>T r.(?) p.(Thr83Ser)
-?/. - c.249T>C r.(?) p.(Thr83=)
-?/. - c.301A>G r.(?) p.(Thr101Ala)
-?/. - c.322C>T r.(?) p.(His108Tyr)
-?/. - c.347C>A r.(?) p.(Pro116His)
-?/. - c.375T>A r.(?) p.(Thr125=)
-?/. - c.394+16G>A r.(=) p.(=)
-?/. - c.394+19G>A r.(=) p.(=)
-/. - c.394+20C>T r.(=) p.(=)
-/. - c.394+20C>T r.(=) p.(=)
-/. - c.394+20C>T r.(=) p.(=)
?/. - c.494A>G r.(?) p.(Gln165Arg)
-?/. - c.516C>A r.(?) p.(Gly172=)
-/. - c.782-14C>T r.(=) p.(=)
-/. - c.782-14C>T r.(=) p.(=)
-/. - c.782-14C>T r.(=) p.(=)
-?/. - c.782-9G>T r.(=) p.(=)
?/. - c.788A>G r.(?) p.(Asn263Ser)
?/. - c.788A>G r.(?) p.(Asn263Ser)
?/. - c.788A>G r.(?) p.(Asn263Ser)
?/. - c.878A>G r.(?) p.(Asp293Gly)
?/. - c.929G>A r.(?) p.(Arg310His)
?/. - c.929G>A r.(?) p.(Arg310His)
?/. - c.938C>T r.(?) p.(Thr313Ile)
-?/. - c.938C>T r.(?) p.(Thr313Ile)
-?/. - c.938C>T r.(?) p.(Thr313Ile)
-?/. - c.938C>T r.(?) p.(Thr313Ile)
-?/. - c.1038C>T r.(?) p.(Ala346=)
-?/. - c.1099C>T r.(?) p.(Arg367Cys)
-?/. - c.1099C>T r.(?) p.(Arg367Cys)
-?/. - c.1104G>C r.(?) p.(Gly368=)
-?/. - c.1104G>C r.(?) p.(Gly368=)
?/. - c.1132G>A r.(?) p.(Ala378Thr)
?/. - c.1132G>A r.(?) p.(Ala378Thr)
-?/. - c.1209-15T>A r.(=) p.(=)
-?/. - c.1209-15T>A r.(=) p.(=)
-?/. - c.1217C>A r.(?) p.(Ala406Glu)
?/. - c.1258T>C r.(?) p.(Tyr420His)
-/. - c.1275T>C r.(?) p.(Tyr425=)
-?/. - c.1275T>C r.(?) p.(Tyr425=)
-?/. - c.1275T>C r.(?) p.(Tyr425=)
-?/. - c.1276C>A r.(?) p.(Arg426Ser)
-?/. - c.1348+9T>C r.(=) p.(=)
-/. - c.1348+9T>C r.(=) p.(=)
-?/. - c.1349-13T>C r.(=) p.(=)
-?/. - c.1349-13T>C r.(=) p.(=)
-?/. - c.1353T>C r.(?) p.(Pro451=)
-?/. - c.1430C>T r.(?) p.(Pro477Leu)
-?/. - c.1430C>T r.(?) p.(Pro477Leu)
-?/. - c.1430C>T r.(?) p.(Pro477Leu)
-?/. - c.1458C>T r.(?) p.(Asn486=)
-?/. - c.1493A>G r.(?) p.(Gln498Arg)
-?/. - c.1501A>C r.(?) p.(Ser501Arg)
?/. - c.1594C>G r.(?) p.(Pro532Ala)
-/. - c.1632= r.(=) p.(Asp544=)
-/. - c.1632= r.(=) p.(Asp544=)
-/. - c.1632= r.(=) p.(Asp544=)
-/. - c.1652C>T r.(?) p.(Thr551Ile)
-/. - c.1652C>T r.(?) p.(Thr551Ile)
-?/. - c.1652C>T r.(?) p.(Thr551Ile)
-/. - c.1652C>T r.(?) p.(Thr551Ile)
-?/. - c.1735T>C r.(?) p.(Tyr579His)
-?/. - c.1818G>A r.(?) p.(Gln606=)
+?/? 10i c.1864+5G>A r.spl? p.?
-?/. - c.1945G>A r.(?) p.(Ala649Thr)
-?/. - c.1945G>A r.(?) p.(Ala649Thr)
+/. - c.1948G>A r.(?) p.(Gly650Arg)
-/. - c.1950A>C r.(?) p.(Gly650=)
-?/. - c.1950A>C r.(=) p.(=)
-?/. - c.1950A>C r.(=) p.(=)
-/. - c.1950A>C r.(?) p.(Gly650=)
-/. - c.1950A>C r.(?) p.(Gly650=)
?/. - c.1960G>A r.(?) p.(Asp654Asn)
-?/. - c.2139T>C r.(?) p.(=)
?/. - c.2158C>T r.(?) p.(Arg720Trp)
?/. - c.2158C>T r.(?) p.(Arg720Trp)
?/. - c.2158C>T r.(?) p.(Arg720Trp)
?/. - c.2158C>T r.(?) p.(Arg720Trp)
?/. - c.2158C>T r.(?) p.(Arg720Trp)
-?/. - c.2191G>C r.(?) p.(Glu731Gln)
-?/. - c.2285+9C>T r.(=) p.(=)
-/. - c.2286-15del r.(=) p.(=)
-/. - c.2286-15del r.(=) p.(=)
-/. - c.2286-15del r.(=) p.(=)
-/. - c.2286-15G>T r.(=) p.(=)
-?/. - c.2286-15G>T r.(=) p.(=)
-?/. - c.2286-15_2286-14del r.(=) p.(=)
-?/. - c.2286-12T>G r.(=) p.(=)
-/. - c.2286-12T>G r.(=) p.(=)
-/. - c.2286-4del r.spl? p.?
-/. - c.2286-4dup r.spl? p.?
-/. - c.2286-4dup r.spl? p.?
-?/. - c.2286-4dup r.spl? p.?
-?/. - c.2287G>T r.(?) p.(Val763Phe)
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