Transcript #00002115 (NM_001111.4, ADAR gene)

Transcript name transcript variant 1
Gene name ADAR (adenosine deaminase, RNA-specific)
Chromosome 1
Transcript - NCBI ID NM_001111.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001102.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-21583C>G r.(?) p.(=)
-?/. - c.-19896T>G r.(?) p.(=)
-/. - c.-19890T>C r.(?) p.(=)
?/. - c.3G>T r.(?) p.?
-?/. - c.9G>A r.(?) p.(Pro3=)
-/. - c.15+10G>T r.(=) p.(=)
-/. - c.15+10G>T r.(=) p.(=)
-/. - c.78G>A r.(?) p.(Arg26=)
-/. - c.78G>A r.(?) p.(Arg26=)
?/. - c.164C>T r.(?) p.(Pro55Leu)
?/. - c.164C>T r.(?) p.(Pro55Leu)
-?/. - c.192G>A r.(?) p.(Leu64=)
+/. 2 c.271_272del r.0? p.0?
?/. - c.289G>A r.(?) p.(Val97Met)
-/. - c.298= r.(=) p.(Gly100=)
-/. - c.298= r.(=) p.(Gly100=)
-?/. - c.487G>A r.(?) p.(Gly163Arg)
?/. - c.487G>A r.(?) p.(Gly163Arg)
-?/. - c.518A>G r.(?) p.(Asn173Ser)
-?/. - c.521G>A r.(?) p.(Arg174Gln)
?/. 2 c.524T>A r.(?) p.(Val175Asp)
+/. 2 c.556C>T r.0? p.0?
+?/+? 2 c.577C>G r.(?) p.(Pro193Ala)
+?/+? 2 c.577C>G r.(?) p.(Pro193Ala)
+?/+ 2 c.577C>G r.(?) p.(Pro193Ala)
+?/+ 2 c.577C>G r.(?) p.(Pro193Ala)
+?/+? 2 c.577C>G r.(?) p.(Pro193Ala)
+?/+? 2 c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>G r.(?) p.(Pro193Ala)
+/. - c.577C>G r.(?) p.(Pro193Ala)
+/. - c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>G r.(?) p.(Pro193Ala)
+/. - c.577C>G r.(?) p.(Pro193Ala)
?/. - c.577C>T r.(?) p.(Pro193Ser)
-?/. - c.674C>T r.(?) p.(Pro225Leu)
-?/. - c.675G>A r.(?) p.(Pro225=)
-?/. - c.675G>A r.(?) p.(Pro225=)
?/. - c.696A>C r.(?) p.(Arg232Ser)
?/. - c.700T>G r.(?) p.(Ser234Ala)
-?/. - c.748G>T r.(?) p.(Ala250Ser)
-?/. - c.772G>A r.(?) p.(Gly258Arg)
+?/. 2 c.788_791del r.(?) p.(Asp263ValfsTer31)
?/. - c.905A>C r.(?) p.(Lys302Thr)
?/. - c.989T>C r.(?) p.(Ile330Thr)
-?/. - c.1003A>T r.(?) p.(Ile335Phe)
?/. - c.1042A>G r.(?) p.(Thr348Ala)
+/. - c.1069_1072del r.(?) p.(Asp357Argfs*47)
+?/+ 2 c.1076_1080del r.(?) p.(Lys359Argfs*14)
+/. - c.1078C>T r.(?) p.(Arg360*)
-?/. - c.1125C>T r.(?) p.(Thr375=)
-/. - c.1151A>G r.(?) p.(Lys384Arg)
-/. - c.1151A>G r.(?) p.(Lys384Arg)
?/. - c.1153del r.(?) p.(Arg385Glufs*20)
-?/. - c.1158C>T r.(?) p.(Asn386=)
-?/. - c.1395T>C r.(?) p.(Ser465=)
-?/. - c.1400G>A r.(?) p.(Arg467His)
?/. - c.1445T>C r.(?) p.(Phe482Ser)
?/. - c.1465C>T r.(?) p.(Arg489Trp)
-?/. - c.1518C>T r.(?) p.(Ser506=)
-?/. - c.1591C>G r.(?) p.(His531Asp)
+/. - c.1601G>A r.1412_1601del p.Gly471Aspfs*30
-?/. - c.1602-6G>A r.(=) p.(=)
-?/. - c.1625A>G r.(?) p.(Asn542Ser)
-?/. - c.1625A>G r.(?) p.(Asn542Ser)
-?/. - c.1625A>G r.(?) p.(Asn542Ser)
?/. - c.1687A>G r.(?) p.(Met563Val)
-?/. - c.1725C>T r.(?) p.(Ala575=)
-?/. - c.1725C>T r.(?) p.(Ala575=)
-?/. - c.1757A>G r.(?) p.(His586Arg)
-/. - c.1760A>G r.(?) p.(Tyr587Cys)
-/. - c.1760A>G r.(?) p.(Tyr587Cys)
-?/. - c.1766C>G r.(?) p.(Thr589Arg)
-?/. - c.1845C>T r.(?) p.(Pro615=)
?/. - c.1846G>A r.(?) p.(Val616Ile)
-?/. - c.1926T>C r.(?) p.(His642=)
-?/. - c.1926T>C r.(?) p.(His642=)
-?/. - c.1926T>C r.(?) p.(His642=)
-?/. - c.1934+8C>T r.(=) p.(=)
-?/. - c.1934+8C>T r.(=) p.(=)
-?/. - c.1935-20C>T r.(=) p.(=)
-?/. - c.1935-20C>T r.(=) p.(=)
-?/. - c.1935-19G>A r.(=) p.(=)
+/. - c.1937_1938insGT r.(?) p.(Phe646Leufs*16)
-?/. - c.2052G>A r.(?) p.(Ala684=)
-?/. - c.2079+7C>T r.(=) p.(=)
-?/. - c.2079+8G>A r.(=) p.(=)
-?/. - c.2079+19C>T r.(=) p.(=)
-?/. - c.2080-5T>C r.spl? p.?
-?/. - c.2107G>C r.(?) p.(Asp703His)
?/. - c.2158G>T r.(?) p.(Val720Leu)
+/. - c.2184_2185insA r.(?) p.(Gly729ArgfsTer15)
-?/. - c.2271-15T>C r.(=) p.(=)
-?/. - c.2275G>A r.(?) p.(Val759Ile)
?/. - c.2275G>A r.(?) p.(Val759Ile)
-?/. - c.2275G>A r.(?) p.(Val759Ile)
?/. - c.2378T>C r.(?) p.(Ile793Thr)
-?/. - c.2496+9G>A r.(=) p.(=)
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