Transcript #00007347 (NM_000128.3, F11 gene)

Transcript name coagulation factor XI
Gene name F11 (coagulation factor XI)
Chromosome 4
Transcript - NCBI ID NM_000128.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000119.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-316C>G r.(?) p.(=)
+/? ? c.94G>A r.(?) p.(Gly32Arg)
+/? ? c.100G>C r.(?) p.(Asp34His)
+/? ? c.127G>A r.(?) p.(Ala43Thr)
+/? ? c.137G>T r.(?) p.(Cys46Phe)
+/? ? c.151A>C r.(?) p.(Thr51Pro)
+/? ? c.151A>C r.(?) p.(Thr51Pro)
+/? ? c.152C>T r.(?) p.(Thr51Ile)
+/? ? c.159C>A r.(?) p.(His53Gln)
+/. - c.166T>C r.(?) p.(Cys56Arg)
+/? ? c.166T>C r.(?) p.(Cys56Arg)
+/? ? c.166T>C r.(?) p.(Cys56Arg)
+/? ? c.188C>T r.(?) p.(Ala63Val)
+/? ? c.197C>T r.(?) p.(Pro66Leu)
+?/. - c.290G>A r.(?) p.(Gly97Glu)
+/? ? c.302A>G r.(?) p.(Lys101Arg)
+/. - c.316C>T r.(?) p.(Gln106*)
?/. - c.325G>A r.(?) p.(Ala109Thr)
+/. - c.325+1G>A r.spl? p.?
?/. - c.344A>G r.(?) p.(Tyr115Cys)
+/. - c.400C>T r.(?) p.(Gln134*)
+/. - c.403G>T r.(?) p.(Glu135Ter)
+/? ? c.419G>A r.(?) p.(Cys140Tyr)
-/. - c.429C>T r.(?) p.(Asp143=)
?/. - c.434A>G r.(?) p.(His145Arg)
+?/. - c.449C>T r.(?) p.(Thr150Met)
+/? ? c.452A>G r.(?) p.(Tyr151Cys)
?/. - c.485G>A r.(?) p.(Arg162His)
?/. - c.617C>G r.(?) p.(Pro206Arg)
+/? ? c.664G>T r.(?) p.(Asp222Tyr)
+/? ? c.683G>A r.(?) p.(Arg228Gln)
+?/. - c.689G>A r.(?) p.(Cys230Tyr)
+/? ? c.723C>G r.(?) p.(Phe241Leu)
+/? ? c.731A>G r.(?) p.(Gln244Arg)
+/? ? c.731A>G r.(?) p.(Gln244Arg)
-/. - c.731A>G r.(?) p.(Gln244Arg)
+/? ? c.738G>C r.(?) p.(Trp246Cys)
+/? ? c.755G>C r.(?) p.(Arg252Thr)
+/. - c.755+1G>A r.spl? p.?
+/. - c.756A>T r.(?) p.(Arg252Ser)
+/? ? c.764G>A r.(?) p.(Cys255Tyr)
+/? ? c.788G>A r.(?) p.(Gly263Glu)
+/? ? c.797G>A r.(?) p.(Ser266Asn)
-/. - c.801A>G r.(?) p.(Thr267=)
+/? ? c.809A>T r.(?) p.(Lys270Ile)
+?/. - c.809A>T r.(?) p.(Lys270Ile)
+/? ? c.827C>G r.(?) p.(Ser276Cys)
+/? ? c.830G>A r.(?) p.(Gly277Asp)
-?/. - c.861C>T r.(?) p.(Ile287=)
?/. - c.866-15T>A r.(=) p.(=)
?/. - c.872G>C r.(?) p.(Cys291Ser)
+/? ? c.901T>C r.(?) p.(Phe301Leu)
+?/. - c.901T>C r.(?) p.(Phe301Leu)
+/. - c.901T>C r.(?) p.(Phe301Leu)
?/. - c.908G>A r.(?) p.(Gly303Glu)
?/. - c.919G>T r.(?) p.(Asp307Tyr)
+/? ? c.922A>T r.(?) p.(Ile308Phe)
+/? ? c.943G>A r.(?) p.(Glu315Lys)
-?/. - c.943G>A r.(?) p.(Glu315Lys)
+/? ? c.959T>C r.(?) p.(Leu320Pro)
+/? ? c.965C>T r.(?) p.(Thr322Ile)
+/? ? c.976C>T r.(?) p.(Arg326Cys)
+/? ? c.992C>T r.(?) p.(Thr331Ile)
+/? ? c.1016G>T r.(?) p.(Cys339Phe)
+/? ? c.1016G>T r.(?) p.(Cys339Phe)
+/? ? c.1021G>A r.(?) p.(Glu341Lys)
+?/. - c.1052C>T r.(?) p.(Ser351Phe)
+/. - c.1075del r.(?) p.(Ile359Tyrfs*13)
+?/. - c.1076T>C r.(?) p.(Ile359Thr)
+/. - c.1076_1077insCGGG r.(?) p.(Leu360GlyfsTer17)
+/? ? c.1079T>C r.(?) p.(Leu360Pro)
?/. - c.1099T>A r.(?) p.(Ser367Thr)
-/. - c.1191T>C r.(?) p.(Gly397=)
+/? ? c.1201T>C r.(?) p.(Trp401Arg)
+/? ? c.1207G>A r.(?) p.(Val403Met)
+/? ? c.1211C>A r.(?) p.(Thr404Asn)
+/. - c.1247G>A r.(?) p.(Cys416Tyr)
+/? ? c.1253G>T r.(?) p.(Gly418Val)
+/? ? c.1289C>T r.(?) p.(Ala430Val)
+/? ? c.1289C>T r.(?) p.(Ala430Val)
?/. - c.1304+6T>C r.(=) p.(=)
+/? ? c.1361T>A r.(?) p.(Ile454Lys)
+/? ? c.1378T>G r.(?) p.(Phe460Val)
+/. - c.1432G>A r.(?) p.(Gly478Arg)
+/? ? c.1442T>G r.(?) p.(Ile481Ser)
?/. - c.1489C>T r.(?) p.(Arg497*)
+/? ? c.1507T>C r.(?) p.(Ser503Pro)
+/? ? c.1517A>G r.(?) p.(Asp506Gly)
+/? ? c.1531T>C r.(?) p.(Tyr511His)
+/? ? c.1541G>T r.(?) p.(Cys514Phe)
+/. - c.1556G>A r.(?) p.(Trp519*)
+/? ? c.1578C>G r.(?) p.(Asp526Glu)
?/. - c.1603G>C r.(?) p.(Ala535Pro)
+/. - c.1608G>C r.(?) p.(Lys536Asn)
+/? ? c.1613C>T r.(?) p.(Pro538Leu)
+?/. - c.1633T>C r.(?) p.(Cys545Arg)
+/. - c.1647C>G r.(?) p.(Tyr549*)
+/? ? c.1693G>A r.(?) p.(Glu565Lys)
-/. - c.1707C>T r.(?) p.(=)
+/. - c.1718G>A r.(?) p.(Gly573Glu)
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