Transcript #00025553 (NM_001135243.1, TCOF1 gene)

Transcript name transcript variant 4
Gene name TCOF1 (Treacher Collins-Franceschetti syndrome 1)
Chromosome 5
Transcript - NCBI ID NM_001135243.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001128715.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2020-09-30 12:22:01 +02:00 (CEST)
Date last edited N/A


Variants

422 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-89T>G r.(?) p.(=)
-?/-? 1 c.-59G>A r.(?) p.(=)
+/+ 1 c.1A>T r.(?) p.0?
+/. - c.3G>A r.(?) p.(Met1?)
+/+ 1 c.3G>A r.(?) p.0?
+/+ 1 c.28del r.(?) p.(Leu10Tyrfs*4)
+/+ 1 c.40A>T r.(?) p.(Ile14Phe)
+/+ 1 c.41del r.(?) p.(Ile14Thrfs*17)
+/+ 1 c.42C>G r.(?) p.(Ile14Met)
+/+ 1 c.48_50del r.(?) p.(His17del)
+/+ 1 c.50A>G r.(?) p.(His17Arg)
?/. - c.58C>T r.(?) p.(Arg20Trp)
+/+ 1 c.61del r.(?) p.(Ala21Leufs*10)
+/+ 1 c.61G>C r.(?) p.(Ala21Pro)
+/+ 1 c.77C>T r.(?) p.(Ala26Val)
+/+ 1 c.79G>A r.(?) p.(Ala27Thr)
+/+ 1 c.87del r.(?) p.(Val30*)
+/+ 1 c.106C>T r.(?) p.(Gln36*)
+/+ 1i c.109-2A>T r.spl p.?
+/+ 1i c.109-1del r.spl p.?
-?/. - c.122C>T r.(?) p.(Ala41Val)
-?/. - c.122C>T r.(?) p.(Ala41Val)
-?/. - c.122C>T r.(?) p.(Ala41Val)
-?/. - c.122C>T r.(?) p.(Ala41Val)
-?/. - c.122C>T r.(?) p.(Ala41Val)
+/. - c.149A>C r.(?) p.(Tyr50Ser)
+/+ 2 c.149A>G r.(?) p.(Tyr50Cys)
+/. - c.149A>G r.(?) p.(Tyr50Cys)
+/. - c.150T>A r.(?) p.(Tyr50*)
+/+ 2 c.157T>C r.(?) p.(Trp53Arg)
+/+ 2 c.159G>A r.(?) p.(Trp53*)
-?/. - c.162A>G r.(?) p.(Gln54=)
+/+ 2 c.163C>T r.(?) p.(Gln55*)
+/. - c.163C>T r.(?) p.(Gln55*)
+/. - c.164+1G>A r.spl? p.?
-?/. - c.187C>T r.(?) p.(Arg63Trp)
-?/. - c.188G>A r.(?) p.(Arg63Gln)
-?/. - c.188G>A r.(?) p.(Arg63Gln)
+/+ 3 c.218_219insAACC r.(?) p.(Lys74Thrfs*2)
-?/. - c.230G>A r.(?) p.(Arg77His)
+/+ 3 c.274del r.(?) p.(Glu92Lysfs*14)
+/+ 3 c.277G>T r.(?) p.(Glu93*)
-?/. - c.295G>A r.(?) p.(Ala99Thr)
-?/. - c.295G>A r.(?) p.(Ala99Thr)
+/+ 3 c.303_304del r.(?) p.(Thr102Profs*72)
+/+ 3i c.304+5G>C r.spl? p.?
+/+ 3i c.305-1G>A r.spl p.?
+/+ 4 c.343del r.(?) p.(Ala115Argfs*7)
+/+ 4 c.357_358del r.(?) p.(Ser120Hisfs*54)
+/+ 4 c.376_378+15del r.spl p.?
+/+ 4i c.379-2A>G r.spl p.?
+/+ 5 c.386_387del r.(?) p.(Thr129Argfs*45)
+/+ 5 c.389dup r.(?) p.(Lys131Glufs*44)
+/+ 5 c.390_391del r.(?) p.(Lys131Serfs*43)
+/+ 5 c.405_406del r.(?) p.(Gly136Glufs*38)
+/+ 5 c.408del r.(?) p.(Asn137Ilefs*82)
+/+ 5 c.422dup r.(?) p.(His141Glnfs*34)
+/+ 5 c.431del r.(?) p.(Thr144Metfs*75)
-?/. - c.440C>T r.(?) p.(Thr147Met)
-?/. - c.449A>G r.(?) p.(Asn150Ser)
+/+ 5 c.475A>T r.(?) p.(Lys159*)
+/+ 5 c.497_500del r.(?) p.(Asn166Ilefs*52)
-?/. 5 c.503C>T r.(?) p.(Thr168Met)
-?/. - c.503C>T r.(?) p.(Thr168Met)
+/+ 5 c.514_515del r.(?) p.(Glu172Asnfs*2)
+/+ 5 c.519del r.(?) p.(Glu174Argfs*45)
-?/. - c.534C>T r.(?) p.(Ser178=)
+/+ 5i c.565+1G>A r.spl p.?
+/+ 5i c.566-10C>A r.spl? p.?
+/. - c.566-1G>A r.spl? p.?
?/. - c.566G>A r.(?) p.(Gly189Glu)
+/+ - c.574_589del r.(?) p.(Ser192Thrfs*22)
-/. - c.579G>A r.(?) p.(Ala193=)
+/+ - c.599del r.(?) p.(Ser200Thrfs*19)
+/+ - c.618del r.(?) p.(Ser207Valfs*12)
+/+ - c.631_632del r.(?) p.(Asp211Argfs*20)
+/+ - c.639+1G>A r.spl p.?
-?/. - c.639+6T>G r.(=) p.(=)
-?/. - c.713C>T r.(?) p.(Ala238Val)
?/. - c.724C>T r.(?) p.(Pro242Ser)
-?/. - c.724C>T r.(?) p.(Pro242Ser)
+/+ - c.726del r.(?) p.(Lys244Argfs*5)
?/. - c.827_844del r.(?) p.(Gly276_Glu281del)
-?/. - c.827_844del r.(?) p.(Gly276_Glu281del)
-?/. - c.827_844del r.(?) p.(Gly276_Glu281del)
-?/. - c.870+1G>A r.spl? p.?
+/+ - c.889del r.(?) p.(Ile297Phefs*30)
+/+ - c.932del r.(?) p.(Pro311Leufs*16)
+/. - c.939dup r.(?) p.(Gly314Argfs*35)
+/+ - c.951_958del r.(?) p.(Ala318Trpfs*28)
+/+ - c.959dup r.(?) p.(Gly321Trpfs*28)
?/. - c.966G>T r.(?) p.(Lys322Asn)
+/+ - c.975dup r.(?) p.(Val326Cysfs*23)
?/. - c.983C>G r.(?) p.(Ser328Cys)
+/. - c.985C>T r.(?) p.(Gln329Ter)
+/+ - c.985C>T r.(?) p.(Gln329*)
-?/. - c.999G>A r.(?) p.(Gly333=)
+/. 8 c.999_1000insT r.(?) p.(Lys334*)
+/+ - c.1016C>G r.(?) p.(Ser339*)
+/+ - c.1017del r.(?) p.(Glu340Argfs*153)
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