Transcript #00007995 (NM_002016.1, FLG gene)

Transcript name filaggrin
Gene name FLG (filaggrin)
Chromosome 1
Transcript - NCBI ID NM_002016.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_002007.1
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

743 entries on 8 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-31972C>T r.(?) p.(=)
-?/. - c.-31911T>C r.(?) p.(=)
-?/. - c.-31664T>A r.(?) p.(=)
?/. - c.-31192C>T r.(?) p.(=)
?/. - c.-31059_-31021del r.(?) p.(=)
?/. - c.-30599G>A r.(?) p.(=)
+/. - c.-30512del r.(?) p.(=)
-?/. - c.-30354C>A r.(?) p.(=)
-/. - c.-30024_-29794del r.(?) p.(=)
-?/. - c.-30024_-29794del r.(?) p.(=)
+?/. - c.-29898C>A r.(?) p.(=)
?/. - c.-29826G>T r.(?) p.(=)
?/. - c.-29518_-29515del r.(?) p.(=)
-?/. - c.-29364A>G r.(?) p.(=)
-?/. - c.-29020G>T r.(?) p.(=)
?/. - c.-28680_-28679dup r.(?) p.(=)
?/. - c.-28680_-28679dup r.(?) p.(=)
?/. - c.-28055del r.(?) p.(=)
-/. - c.-27598A>C r.(?) p.(=)
-?/. - c.-27543T>A r.(?) p.(=)
-?/. - c.-27523C>G r.(?) p.(=)
?/. - c.-27223G>A r.(?) p.(=)
?/. - c.-26789G>A r.(?) p.(=)
?/. - c.63dup r.(?) p.(Asp22Argfs*2)
+/. - c.94G>T r.(?) p.(Glu32*)
+/. - c.94G>T r.(?) p.(Glu32*)
-?/. - c.124C>T r.(?) p.(Arg42Trp)
?/. - c.125G>A r.(?) p.(Arg42Gln)
+/. - c.138+1G>C r.spl? p.?
-?/. - c.139-9T>C r.(=) p.(=)
?/. - c.139-9T>G r.(=) p.(=)
-/. - c.149A>G r.(?) p.(Asp50Gly)
-?/. - c.194A>G r.(?) p.(His65Arg)
?/. - c.209A>C r.(?) p.(Asp70Ala)
-/. - c.284C>T r.(?) p.(Pro95Leu)
-?/. - c.336T>C r.(?) p.(Asp112=)
-?/. - c.498T>G r.(?) p.(Pro166=)
-?/. - c.527A>G r.(?) p.(Asn176Ser)
-?/. - c.558C>A r.(?) p.(Asn186Lys)
?/. - c.754G>A r.(?) p.(Glu252Lys)
-?/. - c.975G>A r.(?) p.(=)
-/. - c.995G>T r.(?) p.(Gly332Val)
?/. - c.1020T>A r.(?) p.(Asp340Glu)
?/. - c.1111T>A r.(?) p.(Ser371Thr)
?/. - c.1157C>G r.(?) p.(Ser386Cys)
?/. - c.1204C>T r.(?) p.(Arg402Cys)
?/. - c.1214C>T r.(?) p.(Ala405Val)
-/. - c.1236T>C r.(?) p.(Arg412=)
-/. - c.1236T>C r.(?) p.(Arg412=)
-/. - c.1255G>A r.(?) p.(Gly419Ser)
?/. - c.1276G>A r.(?) p.(Glu426Lys)
-/. - c.1330G>A r.(?) p.(Gly444Arg)
-?/. - c.1342C>A r.(?) p.(Gln448Lys)
-/. - c.1360A>G r.(?) p.(Thr454Ala)
+/. - c.1378G>T r.(?) p.(Glu460*)
+/. - c.1378G>T r.(?) p.(Glu460*)
?/. - c.1387G>A r.(?) p.(Gly463Arg)
-?/. - c.1432C>T r.(?) p.(Pro478Ser)
-/. - c.1432C>T r.(?) p.(Pro478Ser)
-?/. - c.1455C>T r.(?) p.(Thr485=)
+/. - c.1484C>A r.(?) p.(Ser495*)
-?/. - c.1491C>T r.(?) p.(His497=)
-/. - c.1494G>C r.(?) p.(Glu498Asp)
-?/. - c.1494G>C r.(?) p.(Glu498Asp)
./. - c.1501C>T r.(?) p.(Arg501*)
+?/. - c.1501C>T r.(?) p.(Arg501*)
+/. - c.1501C>T r.(?) p.(Arg501Ter)
+/. - c.1501C>T r.(?) p.(Arg501Ter)
+/. - c.1501C>T r.(?) p.(Arg501Ter)
+/. - c.1501C>T r.(?) p.(Arg501Ter)
./. - c.1501C>T r.(?) p.(Arg501*)
./. - c.1501C>T r.(?) p.(Arg501*)
+?/. - c.1501C>T r.(?) p.(Arg501Ter)
+/+ 3 c.1501C>T r.(?) p.(Arg501*)
+/. - c.1501C>T r.(?) p.(Arg501*)
+/. - c.1501C>T r.(?) p.(Arg501Ter)
?/. - c.1542C>A r.(?) p.(Asp514Glu)
-?/. - c.1573G>A r.(?) p.(Gly525Arg)
-?/. - c.1603T>C r.(?) p.(Ser535Pro)
-/. - c.1683G>C r.(?) p.(Gln561His)
?/. - c.1714C>G r.(?) p.(Arg572Gly)
+/. - c.1714C>T r.(?) p.(Arg572*)
+/. - c.1714C>T r.(?) p.(Arg572*)
-?/. - c.1737C>T r.(?) p.(Asp579=)
-?/. - c.1741A>T r.(?) p.(Thr581Ser)
-?/. - c.1741A>T r.(?) p.(Thr581Ser)
?/. - c.1791C>G r.(?) p.(Ser597Arg)
?/. - c.1813C>T r.(?) p.(Gln605*)
-?/. - c.1828G>A r.(?) p.(Gly610Arg)
?/. - c.1829G>T r.(?) p.(Gly610Val)
?/. - c.1849C>T r.(?) p.(Gln617*)
-?/. - c.1899C>T r.(?) p.(Asp633=)
-/. - c.1992C>A r.(?) p.(His664Gln)
-?/. - c.1993G>A r.(?) p.(Glu665Lys)
-?/. - c.2018C>G r.(?) p.(Ser673Cys)
?/. - c.2023G>C r.(?) p.(Asp675His)
-?/. - c.2023G>C r.(?) p.(Asp675His)
-?/. - c.2036A>T r.(?) p.(Lys679Ile)
?/. - c.2047C>T r.(?) p.(Arg683Cys)
-?/. - c.2052C>A r.(?) p.(His684Gln)
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