Transcript #00001413 (NM_000130.4, F5 gene)

Transcript name coagulation factor V (proaccelerin, labile factor)
Gene name F5 (coagulation factor V (proaccelerin, labile factor))
Chromosome 1
Transcript - NCBI ID NM_000130.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000121.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:31:30 +02:00 (CEST)
Date last edited N/A


Variants

236 entries on 3 pages. Showing entries 1 - 100.
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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.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
-?/. - c.136C>G r.(?) p.(Arg46Gly)
-/. - c.237A>G r.(?) p.(Gln79=)
-/. - c.237A>G r.(?) p.(Gln79=)
-?/. - c.244A>G r.(?) p.(Ile82Val)
?/. - c.251-3832T>C r.(=) p.(=)
+/. 3 c.269T>C r.(?) p.(Leu90Ser)
+?/. - c.283G>A r.(?) p.(Gly95Arg)
+/. 3 c.283G>A r.(?) p.(Gly95Arg)
+/. 3 c.286G>C r.(?) p.(Asp96His)
?/. 3 c.319G>C r.(?) p.(Asp107His)
+/. 3 c.355T>A r.(?) p.(Tyr119Asn)
?/. 4 c.403G>A r.(?) p.(Ala135Thr)
-/. - c.405G>A r.(?) p.(Ala135=)
+/. 4 c.434del r.(?) p.(Gly145Alafs*34)
+/. 4 c.439G>T r.(?) p.(Glu147*)
+/. 4 c.479C>G r.(?) p.(Pro160Arg)
?/. - c.479C>T r.(?) p.(Pro160Leu)
?/. - c.524A>G r.(?) p.(His175Arg)
?/. - c.524A>G r.(?) p.(His175Arg)
-?/. - c.524A>G r.(?) p.(His175Arg)
-/. - c.552G>T r.(?) p.(Ser184=)
+/. 4 c.585del r.(?) p.(Thr197Profs*2)
?/. 5 c.647C>T r.(?) p.(Ala216Val)
+/. 5 c.653T>C r.(?) p.(Phe218Ser)
-?/. - c.676C>G r.(?) p.(Gln226Glu)
+/. 5 c.692T>G r.(?) p.(Met231Arg)
+/. 5 c.706G>T r.(?) p.(Gly236*)
-/. - c.730+7C>T r.(=) p.(=)
+/. 6 c.746C>T r.(?) p.(Ala249Val)
+/. 6 c.763T>C r.(?) p.(Trp255Arg)
+/. 6 c.776G>A r.(?) p.(Gly259Glu)
?/. 6 c.785C>G r.(?) p.(Ser262Trp)
+/. 6 c.785C>T r.(?) p.(Ser262Leu)
+/. 6 c.833A>G r.(?) p.(Gln278Arg)
+/. 6 c.911G>A r.(?) p.(Gly304Glu)
+/. - c.911G>A r.(?) p.(Gly304Glu)
+/. 7 c.1000A>G r.(?) p.(Arg334Gly)
-?/. - c.1000A>G r.(?) p.(Arg334Gly)
+/. 7 c.1001G>C r.(?) p.(Arg334Thr)
?/. - c.1001G>C r.(?) p.(Arg334Thr)
+/. 7 c.1012A>T r.(?) p.(Lys338*)
+/. 7 c.1042_1049del r.(?) p.(Lys348Glyfs*32)
+/. 7 c.1059C>G r.(?) p.(Phe353Leu)
+/. 7 c.1064C>T r.(?) p.(Ala355Val)
+/. 8 c.1128G>T r.(?) p.(Arg376Ser)
+/. 8 c.1160T>C r.(?) p.(Ile387Thr)
-/. - c.1238T>C r.(?) p.(Met413Thr)
?/. 8 c.1238T>C r.(?) p.(Met413Thr)
-/. - c.1242A>G r.(?) p.(Lys414=)
?/. 8 c.1242G>A r.(?) p.(Lys414=)
+/. 8 c.1258G>T r.(?) p.(Gly420Cys)
+/. 9 c.1321C>T r.(?) p.(Arg441Cys)
+/. 9 c.1334T>C r.(?) p.(Ile445Thr)
-/. - c.1380C>T r.(?) p.(Asn460=)
+/. 10 c.1426C>T r.(?) p.(Gln476*)
+/. 10 c.1498T>G r.(?) p.(Cys500Gly)
+/. 10 c.1516_1518del r.(?) p.(Tyr506del)
?/. 10 c.1538G>A r.(?) p.(Arg513Lys)
-/. - c.1538G>A r.(?) p.(Arg513Lys)
+/. 10 c.1561G>A r.(?) p.(Gly521Arg)
+/. 10 c.1599del r.(?) p.(Arg533Serfs*41)
+/. 10 c.1600C>T r.(?) p.(Gln534*)
+/. - c.1601G>A r.(?) p.(Arg534Gln)
+/. 10 c.1601G>A r.1601g>a p.Arg534Gln
+/. 10 c.1601G>A r.(?) p.(Arg534Gln)
+/. 10 c.1601G>A r.(?) p.(Arg534Gln)
+/. 10 c.1601G>A r.(?) p.(Arg534Gln)
+?/. - c.1601G>A r.(?) p.(Arg534Gln)
+?/. - c.1601G>A r.(?) p.(Arg534Gln)
+?/. - c.1601G>A r.(?) p.(Arg534Gln)
+?/. - c.1601G>A r.(?) p.(Arg534Gln)
+?/. - c.1601G>A r.(?) p.(Arg534Gln)
+/. 11 c.1633C>T r.(?) p.(Gln545*)
+/. 11 c.1654G>C r.(?) p.(Asp552His)
+/. 11 c.1673A>C r.(?) p.(Tyr558Ser)
-/. - c.1716G>A r.(?) p.(Glu572=)
+?/. - c.1762+4A>G r.spl? p.?
?/. - c.1837T>C r.(?) p.(Cys613Arg)
+/. 12 c.1837T>C r.(?) p.(Cys613Arg)
+/. 12 c.1852dup r.(?) p.(Gln618Profs*3)
-/. - c.1926C>A r.(?) p.(Thr642=)
?/. - c.1976G>A r.(?) p.(Gly659Glu)
+/. 13 c.2032A>G r.(?) p.(Lys678Glu)
+/. 13 c.2051G>A r.(?) p.(Cys684Tyr)
+/. 13 c.2082G>C r.(?) p.(Glu694Asp)
+/. 13 c.2149_2150del r.(?) p.(Asp717*)
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