Transcript #00007333 (NM_000506.3, F2 gene)

Transcript name coagulation factor II (thrombin)
Gene name F2 (coagulation factor II (thrombin))
Chromosome 11
Transcript - NCBI ID NM_000506.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000497.1
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

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.? r.? p.?
?/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.13C>T r.(?) p.(Arg5*)
+/. 1 c.14G>A r.(?) p.(Arg5Gln)
+/. 2 c.119G>A r.(?) p.(Arg40Gln)
+/. 2 c.124C>T r.(?) p.(Arg42Trp)
+/. 2 c.128G>A r.(?) p.(Arg43Gln)
+/. - c.148G>A r.(?) p.(Glu50Lys)
+/. 2 c.148G>A r.(?) p.(Glu50Lys)
+/. 2 c.175G>C r.(?) p.(Glu59Gln)
+/. 2 c.215A>G r.(?) p.(Glu72Gly)
?/. - c.241-25C>G r.(=) p.(=)
+/. - c.260A>G r.(?) p.(Tyr87Cys)
?/. - c.260A>G r.(?) p.(Tyr87Cys)
+/. 3 c.260A>G r.(?) p.(Tyr87Cys)
-/. - c.266-91T>C r.(=) p.(=)
+/. 4 c.269G>C r.(?) p.(Cys90Ser)
-/. - c.423-7G>C r.(=) p.(=)
-/. - c.423-7G>C r.(=) p.(=)
+/. 6 c.467dup r.(?) p.(Cys157Leufs*60)
+/. 6 c.481G>T r.(?) p.(Asp161Tyr)
-/. - c.494C>T r.(?) p.(Thr165Met)
?/. 6 c.494C>T r.(?) p.(Thr165Met)
+/. 6 c.542G>A r.(?) p.(Cys181Tyr)
-?/. - c.598G>A r.(?) p.(Glu200Lys)
-?/. - c.598G>A r.(?) p.(Glu200Lys)
+/. 7 c.598G>A r.(?) p.(Glu200Lys)
+/. 7 c.787C>T r.(?) p.(Arg263Cys)
+/. 7 c.788G>C r.(?) p.(Arg263Pro)
?/. - c.859G>A r.(?) p.(Asp287Asn)
+/. 8 c.877del r.(?) p.(Glu293Argfs*87)
+/. - c.940C>T r.(?) p.(Arg314Cys)
+/. 8 c.940C>T r.(?) p.(Arg314Cys)
+/. 8 c.941G>A r.(?) p.(Arg314His)
+/. 9 c.1024T>G r.(?) p.(Phe342Val)
+/. 9 c.1027G>A r.(?) p.(Glu343Lys)
+/. 9 c.1033_1035del r.(?) p.(Lys345del)
+/. 9 c.1054G>A r.(?) p.(Glu352Lys)
+/. 9 c.1084G>A r.(?) p.(Gly362Arg)
+/. 9 c.1088G>A r.(?) p.(Arg363His)
+/. 9 c.1117G>A r.(?) p.(Gly373Ser)
+/. 10 c.1139T>C r.(?) p.(Met380Thr)
+/. 10 c.1147C>T r.(?) p.(Arg383Trp)
+/. 10 c.1189A>C r.(?) p.(Ser397Arg)
+/. 10 c.1200G>T r.(?) p.(Trp400Cys)
+/. 10 c.1213G>A r.(?) p.(Ala405Thr)
-/. - c.1233G>A r.(?) p.(Pro411=)
+/. 10 c.1273C>T r.(?) p.(Arg425Cys)
+/. 10 c.1274G>A r.(?) p.(Arg425His)
+/. 10 c.1292G>A r.(?) p.(Arg431His)
./. - c.1303G>A r.(?) p.(Glu435Lys)
+/. 11 c.1381C>T r.(?) p.(Arg461Trp)
+/. 12 c.1499G>A r.(?) p.(Arg500Gln)
+/. 12 c.1526A>C r.(?) p.(Glu509Ala)
+/. 12 c.1555C>T r.(?) p.(Gln519*)
-/. - c.1602G>A r.(?) p.(Pro534=)
?/. - c.1602G>A r.(=) p.(=)
+/. 13 c.1672_1676del r.(?) p.(Gly558Thrfs*6)
+/. 13 c.1679G>A r.(?) p.(Arg560Gln)
+?/. - c.1686T>A r.(?) p.(Asp562Glu)
+/. 13 c.1688C>T r.(?) p.(Ala563Val)
-/. - c.1726-59G>A r.(=) p.(=)
+/. 14 c.1741C>T r.(?) p.(Arg581Cys)
+/. 14 c.1750C>T r.(?) p.(Gln584*)
+/. 14 c.1772G>C r.(?) p.(Gly591Ala)
+/. 14 c.1785C>G r.(?) p.(Asp595Glu)
+/. 14 c.1796A>C r.(?) p.(Lys599Thr)
+/. 14 c.1802G>T r.(?) p.(Gly601Val)
+/. 14 c.1814A>G r.(?) p.(His605Arg)
+/. 14 c.1818_1819del r.(?) p.(Phe607Profs*11)
+/. 14 c.1835G>A r.(?) p.(Trp612*)
+/. - c.*97G>A r.(=) p.(=)
+/. - c.*97G>A r.(=) p.(=)
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