Transcript #00003192 (NM_003502.3, AXIN1 gene)

Transcript name transcript variant 1
Gene name AXIN1 (axin 1)
Chromosome 16
Transcript - NCBI ID NM_003502.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003493.1
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

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-19C>A r.(?) p.(=)
./. - c.137C>T r.(?) p.(Ser46Phe)
?/. - c.187C>T r.(?) p.(Arg63Cys)
./. - c.188G>A r.(?) p.(Arg63His)
-?/. - c.299G>A r.(?) p.(Ser100Asn)
./. - c.299G>A r.(?) p.(Ser100Asn)
./. - c.400G>A r.(?) p.(Glu134Lys)
./. - c.586A>G r.(?) p.(Asn196Asp)
-?/. - c.644C>T r.(?) p.(Ser215Leu)
-/. - c.762T>C r.(?) p.(Asp254=)
./. - c.787C>A r.(?) p.(Pro263Thr)
./. - c.805C>G r.(?) p.(Gln269Glu)
-?/. - c.833C>T r.(?) p.(Pro278Leu)
./. - c.833C>T r.(?) p.(Pro278Leu)
?/. - c.833C>T r.(?) p.(Pro278Leu)
?/. - c.871G>C r.(?) p.(Glu291Gln)
-?/. - c.878+8C>T r.(=) p.(=)
./. - c.964G>A r.(?) p.(Glu322Lys)
./. - c.1007C>A r.(?) p.(Thr336Lys)
?/. - c.1007C>T r.(?) p.(Thr336Met)
?/. - c.1030C>T r.(?) p.(Pro344Ser)
?/. - c.1054C>A r.(?) p.(His352Asn)
?/. - c.1074G>C r.(?) p.(Glu358Asp)
-/. - c.1116+20T>C r.(=) p.(=)
./. - c.1127G>A r.(?) p.(Arg376Gln)
-?/. - c.1133C>G r.(?) p.(Pro378Arg)
./. - c.1144C>T r.(?) p.(Arg382Cys)
-?/. - c.1145G>A r.(?) p.(Arg382His)
./. - c.1145G>A r.(?) p.(Arg382His)
./. - c.1147G>A r.(?) p.(Val383Met)
./. - c.1205C>T r.(?) p.(Thr402Met)
?/. - c.1205C>T r.(?) p.(Thr402Met)
?/. - c.1244G>A r.(?) p.(Arg415His)
?/. - c.1244G>A r.(?) p.(Arg415His)
-/. - c.1254+17G>A r.(=) p.(=)
?/. - c.1378C>T r.(?) p.(Arg460Trp)
?/. - c.1417G>A r.(?) p.(Glu473Lys)
-?/. - c.1576G>A r.(?) p.(Ala526Thr)
-?/. - c.1577C>T r.(?) p.(Ala526Val)
-?/. - c.1602C>A r.(?) p.(His534Gln)
-?/. - c.1677G>A r.(?) p.(Gln559=)
?/. - c.1784+3G>C r.spl? p.?
./. - c.1798G>A r.(?) p.(Val600Met)
./. - c.1838A>G r.(?) p.(Lys613Arg)
-?/. - c.1948G>A r.(?) p.(Gly650Ser)
./. - c.1948G>A r.(?) p.(Gly650Ser)
./. - c.1948G>A r.(?) p.(Gly650Ser)
./. - c.1948G>A r.(?) p.(Gly650Ser)
-?/. - c.1982C>A r.(?) p.(Pro661His)
-?/. - c.1989G>T r.(?) p.(Glu663Asp)
-?/. - c.2129C>T r.(?) p.(Ala710Val)
+/. - c.2167C>T r.(?) p.(Arg723Ter)
+/. - c.2167C>T r.(?) p.(Arg723Ter)
+/. - c.2167C>T r.(?) p.(Arg723Ter)
+/. - c.2167C>T r.(?) p.(Arg723Ter)
-?/. - c.2186+4C>T r.spl? p.?
-?/. - c.2186+4C>T r.spl? p.?
?/. - c.2197G>T r.(?) p.(Glu733Ter)
?/. - c.2234C>T r.(?) p.(Ala745Val)
?/. - c.2243C>T r.(?) p.(Pro748Leu)
-?/. - c.2243C>T r.(?) p.(Pro748Leu)
./. - c.2303C>T r.(?) p.(Ser768Leu)
+/. - c.2395dup r.(?) p.(Val799GlyfsTer4)
+/. - c.2395dup r.(?) p.(Val799GlyfsTer4)
-?/. - c.2410G>A r.(?) p.(Ala804Thr)
+/. - c.2413C>T r.(?) p.(Arg805Ter)
?/. - c.2462G>C r.(?) p.(Arg821Thr)
./. - c.2522G>A r.(?) p.(Arg841Gln)
./. - c.2563A>G r.(?) p.(Ile855Val)
-?/. - c.*1233dup r.(?) p.(=)
?/. - c.*1256T>C r.(=) p.(=)
-?/. - c.*1392G>T r.(=) p.(=)
?/. - c.*1709C>T r.(=) p.(=)
?/. - c.*2414C>T r.(=) p.(=)
-?/. - c.*2483C>A r.(=) p.(=)
?/. - c.*2574C>G r.(=) p.(=)
?/. - c.*2704G>A r.(=) p.(=)
-?/. - c.*2738G>A r.(=) p.(=)
-?/. - c.*2971C>A r.(=) p.(=)
-?/. - c.*3025C>G r.(=) p.(=)
?/. - c.*3202G>A r.(=) p.(=)
?/. - c.*3425G>A r.(=) p.(=)
-?/. - c.*3591G>A r.(=) p.(=)
-?/. - c.*3742G>A r.(=) p.(=)
?/. - c.*4783C>T r.(=) p.(=)
-?/. - c.*4838G>A r.(=) p.(=)
-?/. - c.*4852G>A r.(=) p.(=)
-?/. - c.*4926_*4928dup r.(=) p.(=)
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