Transcript #00005902 (NM_001913.3, CUX1 gene)

Transcript name transcript variant 2
Gene name CUX1 (cut-like homeobox 1)
Chromosome 7
Transcript - NCBI ID NM_001913.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001904.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

66 entries on 1 page. Showing entries 1 - 66.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.19T>C r.(?) p.(Ser7Pro)
-?/. - c.63+9C>T r.(=) p.(=)
-?/. - c.63+1584G>A r.(=) p.(=)
-?/. - c.63+47589_63+47590del r.(=) p.(=)
-?/. - c.175-36414G>A r.(=) p.(=)
-?/. - c.175-20896C>T r.(=) p.(=)
-?/. - c.223-18185G>A r.(=) p.(=)
-?/. - c.295G>A r.(?) p.(Val99Ile)
-?/. - c.302-4G>A r.spl? p.?
?/. - c.353G>A r.(?) p.(Arg118His)
?/. - c.671A>T r.(?) p.(Asp224Val)
?/. - c.688G>A r.(?) p.(Asp230Asn)
-?/. - c.707+9C>T r.(=) p.(=)
-?/. - c.709G>A r.(?) p.(Ala237Thr)
?/. - c.983G>A r.(?) p.(Arg328Gln)
?/. - c.992C>T r.(?) p.(Ser331Leu)
-?/. - c.1109+9G>A r.(=) p.(=)
-?/. - c.1255+1093C>T r.(=) p.(=)
?/. - c.1255+1155C>G r.(=) p.(=)
?/. - c.1255+1158G>C r.(=) p.(=)
-?/. - c.1255+1213A>G r.(=) p.(=)
-?/. - c.1255+1213A>G r.(=) p.(=)
?/. - c.1255+1388C>T r.(=) p.(=)
-?/. - c.1255+1593A>G r.(=) p.(=)
+?/. - c.1255+1596G>A r.(=) p.(=)
-?/. - c.1255+5749C>T r.(=) p.(=)
-?/. - c.1255+5797C>G r.(=) p.(=)
?/. - c.1255+5814G>A r.(=) p.(=)
-?/. - c.1255+6026C>T r.(=) p.(=)
?/. - c.1255+6199C>T r.(=) p.(=)
+?/. - c.1255+6278C>T r.(=) p.(=)
?/. - c.1255+6338T>C r.(=) p.(=)
-?/. - c.1255+6461A>C r.(=) p.(=)
?/. - c.1255+6583G>A r.(=) p.(=)
-?/. - c.1255+9521C>T r.(=) p.(=)
-?/. - c.1255+23489_1255+23492del r.(=) p.(=)
-?/. - c.1255+23491_1255+23492dup r.(=) p.(=)
-?/. - c.1255+31961G>A r.(=) p.(=)
?/. - c.1255+32001C>G r.(=) p.(=)
-?/. - c.1255+32001C>G r.(=) p.(=)
?/. - c.1255+32002C>T r.(=) p.(=)
-?/. - c.1255+32002C>T r.(=) p.(=)
-?/. - c.1255+32033C>A r.(=) p.(=)
?/. - c.1256-24764T>G r.(=) p.(=)
-?/. - c.1256-24730G>A r.(=) p.(=)
-?/. - c.1256-24587G>C r.(=) p.(=)
-?/. - c.1256-24535C>G r.(=) p.(=)
-?/. - c.1256-24535C>G r.(=) p.(=)
-?/. - c.1256-24535C>T r.(=) p.(=)
-?/. - c.1256-24520C>G r.(=) p.(=)
-?/. - c.1256-24445C>T r.(=) p.(=)
-?/. - c.1256-24408C>A r.(=) p.(=)
-?/. - c.1256-9691A>C r.(=) p.(=)
-?/. - c.1265C>T r.(?) p.(Ala422Val)
-?/. - c.1384G>A r.(?) p.(Gly462Ser)
-?/. - c.1384G>A r.(?) p.(Gly462Ser)
?/. - c.1543C>T r.(?) p.(Arg515Trp)
-?/. - c.1544G>A r.(?) p.(Arg515Gln)
+?/. - c.1563+1G>A r.spl? p.?
-?/. - c.1624G>A r.(?) p.(Ala542Thr)
-?/. - c.1633A>G r.(?) p.(Ile545Val)
-?/. - c.1636A>C r.(?) p.(Lys546Gln)
-?/. - c.1699A>G r.(?) p.(Thr567Ala)
?/. - c.1708C>T r.(?) p.(Arg570Trp)
?/. - c.1902+1G>T r.spl? p.?
-?/. - c.1903-5G>C r.spl? p.?
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