Transcript #00025585 (NM_015069.3, ZNF423 gene)

Transcript name transcript variant 1
Gene name ZNF423 (zinc finger protein 423)
Chromosome 16
Transcript - NCBI ID NM_015069.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_055884.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-11-26 19:39:56 +01:00 (CET)
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.-33069G>A r.(?) p.(=)
-?/. - c.-5112dup r.(?) p.(=)
-?/. - c.10A>G r.(?) p.(Lys4Glu)
?/. - c.10A>G r.(?) p.(Lys4Glu)
-/. - c.10A>G r.(?) p.(Lys4Glu)
?/. - c.11A>C r.(?) p.(Lys4Thr)
-?/. - c.17-7_17-6del r.(=) p.(=)
-?/. - c.63C>T r.(?) p.(Ser21=)
-?/. - c.76+8C>T r.(=) p.(=)
-?/. - c.76+8C>T r.(=) p.(=)
-/. - c.76+8C>T r.(=) p.(=)
-?/. - c.76+9C>G r.(=) p.(=)
-?/. - c.76+13G>A r.(=) p.(=)
-/. - c.76+13G>A r.(=) p.(=)
?/. - c.173A>C r.(?) p.(Asp58Ala)
?/. - c.185A>C r.(?) p.(Glu62Ala)
-?/. - c.185A>C r.(?) p.(Glu62Ala)
?/. - c.208G>A r.(?) p.(Asp70Asn)
+/. - c.266G>A r.(?) p.(Arg89His)
-/. - c.278-49C>T r.(=) p.(=)
-?/. - c.288C>T r.(?) p.(Asp96=)
-/. - c.288C>T r.(?) p.(Asp96=)
?/. - c.293C>G r.(?) p.(Pro98Arg)
-/. - c.429C>T r.(?) p.(Cys143=)
-?/. - c.429C>T r.(?) p.(Cys143=)
-/. - c.543T>C r.(?) p.(Arg181=)
-?/. - c.654C>T r.(?) p.(Ser218=)
-?/. - c.687C>T r.(?) p.(Arg229=)
-/. - c.687C>T r.(?) p.(Arg229=)
-/. - c.687C>T r.(?) p.(Arg229=)
-?/. - c.688G>A r.(?) p.(Gly230Ser)
-?/. - c.761C>T r.(?) p.(Ser254Leu)
-?/. - c.783C>T r.(?) p.(=)
?/. - c.802T>G r.(?) p.(Cys268Gly)
?/. 4 c.955G>A r.(?) p.(Ala319Thr)
?/. 4 c.955G>A r.(?) p.(Ala319Thr)
?/. 5 c.1059C>A r.(?) p.(His353Gln)
?/. - c.1099A>G r.(?) p.(Met367Val)
?/. - c.1100T>G r.(?) p.(Met367Arg)
-?/. - c.1107C>T r.(?) p.(Ser369=)
-?/. - c.1107C>T r.(?) p.(Ser369=)
-?/. - c.1108G>A r.(?) p.(Ala370Thr)
-?/. - c.1125C>T r.(?) p.(Ser375=)
?/. - c.1144T>C r.(?) p.(Ser382Pro)
?/. - c.1144T>C r.(?) p.(Ser382Pro)
?/. - c.1168C>T r.(?) p.(Pro390Ser)
-?/. - c.1170G>A r.(?) p.(Pro390=)
-?/. - c.1170G>A r.(?) p.(Pro390=)
?/. - c.1229G>A r.(?) p.(Ser410Asn)
?/. - c.1270G>A r.(?) p.(Val424Met)
-?/. - c.1301C>T r.(?) p.(Ala434Val)
-?/. - c.1302G>A r.(?) p.(Ala434=)
-?/. - c.1302G>A r.(?) p.(Ala434=)
-/. - c.1323C>T r.(?) p.(His441=)
-/. - c.1341G>C r.(?) p.(Leu447=)
-?/. - c.1341G>C r.(?) p.(Leu447=)
-?/. - c.1371C>T r.(?) p.(Asn457=)
?/. - c.1378G>A r.(?) p.(Val460Ile)
?/. - c.1378G>A r.(?) p.(Val460Ile)
?/. - c.1382G>A r.(?) p.(Arg461His)
?/. - c.1471G>T r.(?) p.(Asp491Tyr)
?/. - c.1520A>G r.(?) p.(Asn507Ser)
+?/. - c.1537G>A r.(?) p.(Gly513Ser)
?/. - c.1554C>G r.(?) p.(Phe518Leu)
?/. - c.1559A>G r.(?) p.(Asn520Ser)
-?/. - c.1628T>C r.(?) p.(Val543Ala)
-?/. - c.1631G>T r.(?) p.(Gly544Val)
-/. - c.1653G>A r.(?) p.(Pro551=)
-?/. - c.1728C>T r.(?) p.(Ser576=)
+?/. - c.1801G>A r.(?) p.(Ala601Thr)
-?/. - c.1824C>T r.(?) p.(Ser608=)
-/. - c.1845G>A r.(=) p.(=)
-/. - c.1845G>A r.(=) p.(=)
-?/. - c.1850G>A r.(?) p.(Arg617Gln)
-/. - c.1886A>G r.(?) p.(Asn629Ser)
-/. - c.1886A>G r.(?) p.(Asn629Ser)
-/. - c.1886A>G r.(?) p.(Asn629Ser)
-?/. - c.1959G>A r.(?) p.(Leu653=)
-/. - c.1962C>T r.(?) p.(His654=)
?/. - c.1982A>C r.(?) p.(Lys661Thr)
-/. - c.1989G>A r.(?) p.(Ala663=)
-?/. - c.1989G>A r.(?) p.(Ala663=)
-?/. - c.1989G>T r.(?) p.(Ala663=)
-?/. - c.2064G>A r.(?) p.(Thr688=)
?/. - c.2108C>T r.(?) p.(Ser703Leu)
-?/. - c.2109G>A r.(?) p.(Ser703=)
-?/. - c.2109G>A r.(?) p.(Ser703=)
?/. - c.2288C>T r.(?) p.(Ala763Val)
-/. - c.2304C>T r.(?) p.(His768=)
-/. - c.2376C>T r.(?) p.(Thr792=)
-?/. - c.2507C>T r.(?) p.(Ala836Val)
-?/. - c.2507C>T r.(?) p.(Ala836Val)
?/. - c.2507C>T r.(?) p.(Ala836Val)
-?/. - c.2511C>T r.(?) p.(Thr837=)
-?/. - c.2517C>T r.(?) p.(Asn839=)
?/. - c.2616T>C r.(?) p.(His872=)
?/. - c.2734C>T r.(?) p.(Arg912Trp)
?/. - c.2738C>T r.(?) p.(Pro913Leu)
?/. - c.2738C>T r.(?) p.(Pro913Leu)
?/. - c.2758C>T r.(?) p.(Arg920Cys)
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