Transcript #00023136 (NM_024721.4, ZFHX4 gene)

Transcript name zinc finger homeobox 4
Gene name ZFHX4 (zinc finger homeobox 4)
Chromosome 8
Transcript - NCBI ID NM_024721.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_078997.4
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

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-46-8T>G r.(=) p.(=)
-?/. - c.490G>A r.(?) p.(Ala164Thr)
+?/. - c.703_704del r.(?) p.(Lys235Glufs*9)
?/. - c.827C>A r.(?) p.(Pro276His)
?/. - c.866A>G r.(?) p.(Tyr289Cys)
-?/. - c.1030G>A r.(?) p.(Val344Ile)
?/. - c.1146A>T r.(?) p.(Leu382Phe)
-?/. - c.1177G>C r.(?) p.(Glu393Gln)
?/. - c.1223del r.(?) p.(Leu408ArgfsTer7)
-?/. - c.1475C>T r.(?) p.(Thr492Ile)
?/. - c.1505T>C r.(?) p.(Leu502Pro)
?/. - c.1505T>C r.(?) p.(Leu502Pro)
?/. - c.1574C>T r.(?) p.(Ser525Phe)
-?/. - c.1790C>T r.(?) p.(Thr597Ile)
?/. - c.1866G>T r.(?) p.(Leu622Phe)
?/. - c.1910C>G r.(?) p.(Ser637Trp)
?/. - c.2081G>A r.(?) p.(Cys694Tyr)
?/. - c.2114A>G r.(?) p.(Asn705Ser)
?/. - c.2335G>T r.(?) p.(Ala779Ser)
-?/. - c.2488G>C r.(?) p.(Gly830Arg)
-?/. - c.2591-3T>C r.spl? p.?
+?/. - c.3093+1G>T r.spl p.?
?/. - c.3319G>A r.(?) p.(Glu1107Lys)
?/. - c.3361_3363dup r.(?) p.(Asp1121dup)
-/. - c.3387G>A r.(?) p.(Ser1129=)
+/. - c.3646-1G>A r.spl p.?
-?/. - c.3683A>T r.(?) p.(Asp1228Val)
-?/. - c.3760G>A r.(?) p.(Val1254Ile)
?/. - c.3777G>A r.(?) p.(Met1259Ile)
-?/. - c.3991A>G r.(?) p.(Met1331Val)
-?/. - c.4118C>A r.(?) p.(Thr1373Lys)
-?/. - c.4188G>T r.(?) p.(Lys1396Asn)
?/. - c.4202A>G r.(?) p.(His1401Arg)
-?/. - c.4336G>A r.(?) p.(Ala1446Thr)
?/. - c.4564C>T r.(?) p.(Pro1522Ser)
?/. - c.4912A>G r.(?) p.(Ile1638Val)
?/. - c.5048C>T r.(?) p.(Pro1683Leu)
-?/. - c.5176C>A r.(?) p.(Pro1726Thr)
?/. - c.5200C>A r.(?) p.(Gln1734Lys)
-?/. - c.5361C>T r.(?) p.(His1787=)
-?/. - c.5384T>C r.(?) p.(Ile1795Thr)
?/. - c.5656A>T r.(?) p.(Lys1886Ter)
?/. - c.5888G>T r.(?) p.(Ser1963Ile)
?/. - c.5948G>A r.(?) p.(Arg1983His)
?/. - c.6352G>A r.(?) p.(Gly2118Arg)
-/. - c.6708C>T r.(?) p.(Tyr2236=)
?/. - c.6791A>G r.(?) p.(Asn2264Ser)
?/. - c.6914T>C r.(?) p.(Ile2305Thr)
-?/. - c.7200G>C r.(?) p.(Glu2400Asp)
-?/. - c.7222T>C r.(?) p.(Tyr2408His)
?/. - c.7352_7357del r.(?) p.(Gln2451_Pro2452del)
?/. - c.7548C>G r.(?) p.(Phe2516Leu)
?/. - c.7781_7783del r.(?) p.(Glu2594del)
?/. - c.8309C>T r.(?) p.(Pro2770Leu)
?/. - c.8473A>T r.(?) p.(Ser2825Cys)
?/. - c.8847T>G r.(?) p.(Ser2949Arg)
-?/. - c.9047A>T r.(?) p.(Tyr3016Phe)
?/. - c.9126_9130del r.(?) p.(Leu3043SerfsTer21)
?/. - c.9268C>T r.(?) p.(His3090Tyr)
?/. - c.9331G>A r.(?) p.(Gly3111Arg)
?/. - c.9413T>G r.(?) p.(Phe3138Cys)
-?/. - c.9431C>T r.(?) p.(Ser3144Leu)
-?/. - c.9517_9519del r.(?) p.(Pro3173del)
?/. - c.9517_9519dup r.(?) p.(Pro3173dup)
?/. - c.9594G>T r.(?) p.(Lys3198Asn)
?/. - c.9701G>A r.(?) p.(Gly3234Asp)
?/. - c.9701G>A r.(?) p.(Gly3234Asp)
-?/. - c.10022A>C r.(?) p.(Gln3341Pro)
?/. - c.10381G>A r.(?) p.(Ala3461Thr)
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