Transcript #00010758 (NM_006121.3, KRT1 gene)

Transcript name keratin 1
Gene name KRT1 (keratin 1)
Chromosome 12
Transcript - NCBI ID NM_006121.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006112.3
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.75C>T r.(=) p.(=)
-?/. - c.75C>T r.(=) p.(=)
?/. - c.112C>T r.(?) p.(Arg38Cys)
?/. - c.113G>A r.(?) p.(Arg38His)
-?/. - c.193C>T r.(?) p.(Arg65Trp)
+/. 1 c.221A>T r.(?) p.(Lys74Ile)
-?/. - c.315T>G r.(?) p.(Gly105=)
-?/. - c.318_332del r.(?) p.(Phe109_Gly113del)
+/. 1 c.464T>A r.(?) p.(Val155Asp)
+/. 1 c.464T>G r.(?) p.(Val155Gly)
+/. 1 c.482T>C r.(?) p.(Leu161Pro)
-/. 1 c.507_518del r.(?) p.(Asp170_Ile173del)
+/. 1 c.531G>T r.(?) p.(Lys177Asn)
+/. 1 c.536G>C r.(?) p.(Arg179Pro)
+/. 1 c.556T>C r.(?) p.(Ser186Pro)
+/. 1 c.559C>T r.(?) p.(Leu187Phe)
+/. 1 c.559C>T r.(?) p.(Leu187Phe)
+/. 1 c.563A>C r.(?) p.(Asn188Thr)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.563A>G r.(?) p.(Asn188Ser)
+/. - c.563A>G r.(?) p.(Asn188Ser)
+/. 1 c.564C>A r.(?) p.(Asn188Lys)
+/. 1 c.564C>A r.(?) p.(Asn188Lys)
+/. 1 c.571T>A r.(?) p.(Phe191Ile)
+/. 1 c.572T>G r.(?) p.(Phe191Cys)
+/. 1 c.577T>C r.(?) p.(Ser193Pro)
+/. 1i c.591+1G>A r.526_591del p.(Val176_Lys197del)
+/. 1i c.591+1G>C r.526_591del p.(Val176_Lys197del)
+/. 1i c.591+2T>A r.526_591del p.(Val176_Lys197del)
+/. 1i c.591+2T>A r.526_591del p.(Val176_Lys197del)
+/. 1i c.591+3_591+6del r.526_591del p.(Val176_Lys197del)
-?/. - c.592-8G>A r.(=) p.(=)
-?/. - c.592-8G>A r.(=) p.(=)
+/. 2 c.623T>C r.(?) p.(Leu208Pro)
+/. 2 c.641T>C r.(?) p.(Leu214Pro)
?/. - c.655G>T r.(?) p.(Asp219Tyr)
+/. 2 c.693T>G r.(?) p.(Phe231Leu)
+/. 2 c.698C>T r.(?) p.(Ser233Leu)
+/. 2 c.698C>T r.(?) p.(Ser233Leu)
+/. 2 c.698C>T r.(?) p.(Ser233Leu)
+/. 2 c.698C>T r.(?) p.(Ser233Leu)
-/. 2 c.720G>A r.(?) p.(=)
?/. - c.761C>T r.(?) p.(Ser254Leu)
?/. - c.800G>A r.(?) p.(Arg267Gln)
-/. 2 c.800G>A r.(?) p.(Arg267Gln)
?/. - c.956A>G r.(?) p.(Tyr319Cys)
+?/. - c.1018G>T r.(?) p.(Asp340Tyr)
+/. 5 c.1019A>G r.(?) p.(Asp340Gly)
+/. 5 c.1019A>G r.(?) p.(Asp340Gly)
+/. 5 c.1019A>G r.(?) p.(Asp340Gly)
+/. - c.1019A>G r.(?) p.(Asp340Gly)
+/. - c.1019A>G r.(?) p.(Asp340Gly)
+/. 5 c.1019A>T r.(?) p.(Asp340Val)
+/. - c.1019A>T r.(?) p.(Asp340Val)
?/. - c.1028G>A r.(?) p.(Arg343His)
-/. 5 c.1072A>T r.(?) p.(Asn358Tyr)
+/. 5i_6i c.1129-30_1254+286delins214 r.1129_1254del p.(Tyr377_Gln418del)
+/. 6i c.1254+1G>A r.1254+1_1254+54ins p.(Gln418_Ile419ins18)
-?/. - c.1254+7G>T r.(=) p.(=)
+?/. 14 c.1255-4del r.spl? p.?
+/. 6i c.1255-1G>C r.spl p.?
+/. 7 c.1310T>C r.(?) p.(Leu437Pro)
-?/. - c.1360G>T r.(?) p.(Ala454Ser)
+/. 7 c.1376_1399del r.(?) p.(Ala459_Gln466del)
?/. - c.1379G>C r.(?) p.(Arg460Pro)
-/. 7 c.1389C>T r.(?) p.(=)
-/. - c.1389C>T r.(?) p.(Arg463=)
?/. - c.1397A>G r.(?) p.(Gln466Arg)
-/. - c.1413= r.(=) p.(Thr471=)
-/. 7 c.1413C>A r.(?) p.(=)
+/. 7 c.1432G>A r.(?) p.(Glu478Lys)
+/. 7 c.1432G>C r.(?) p.(Glu478Gln)
+/. 7 c.1434G>T r.(?) p.(Glu478Asp)
+/. 7 c.1434G>T r.(?) p.(Glu478Asp)
+/. 7 c.1434G>T r.(?) p.(Glu478Asp)
+/. 7 c.1435A>T r.(?) p.(Ile479Phe)
+/. 7 c.1435A>T r.(?) p.(Ile479Phe)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1436T>C r.(?) p.(Ile479Thr)
+/. 7 c.1441A>C r.(?) p.(Thr481Pro)
+/. 7 c.1445A>G r.(?) p.(Tyr482Cys)
+/. 7 c.1454T>C r.(?) p.(Leu485Pro)
+/. 7 c.1457T>C r.(?) p.(Leu486Pro)
+/. 7 c.1457T>C r.(?) p.(Leu486Pro)
+/. 7 c.1457T>G r.(?) p.(Leu486Arg)
+/. 7 c.1465G>A r.(?) p.(Glu489Lys)
+/. 7 c.1468G>A r.(?) p.(Glu490Lys)
+/. 7 c.1468G>C r.(?) p.(Glu490Gln)
+/. 7 c.1469A>G r.(?) p.(Glu490Gly)
?/. - c.1480T>G r.(?) p.(Ser494Ala)
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