Home > Mutations Untitled Document The mutations reported for Combined Factor V and VIII deficiency are listed below: Missense Position* Wild type Mutant Domain PMID 81 AspHis 2049195881 AspTyr 1914116089 AspAla 16304051, 1839107789 AspAsn 21492322100 ValAsp 20491958122 AspVal 18391077, 17610559129 AspGlu 12717434135 TyrAsn 18685427136 IleThr 16304051, 12717434 Insertion Mutation Codon Exon/Intron Domain PMID 89-90insG Exon 1 Lectin 10090935, 10090934, 18391077 912-913insA Exon 8 10090934 1208-1209insT Exon 10 10090934 Deletion Mutation Codon Exon/Intron Domain PMID 23delG Exon 1 10090934 31delG Exon 1 Lectin 10090934 8.4 kb deletion Exon 1 17971482 103delC Exon 2 12717434 422delC Exon 3 Lectin 10090935 210-244del35-bp Exon 3 EF1 17610559 249delT Exon 3 EF1 12717434 263del8-bp Exon 3 EF1 12717434 374-375delGA Exon 3 EF1 18391077 720del16-bp Exon 6 Lectin 10090935 780-781delT Exon 7 Lectin 16304051 795delC Exon 7 Lectin 18391077 813-822del72-bp Exon 7 Lectin 17610559 839-841delA Exon 8 16304051 1109delTC Exon 9 10090935 1214-1218delAAATG Exon 10 10090934 1271delG Exon 11 16676083 1356delC Exon 11 18391077 1524delA Exon 13 10090935 Nonsense Mutation* Codon Exon/Intron Domain PMID Gly114X Exon 2 Lectin 16044454 Ser144X Exon 4 EF2 17971482 Arg202X Exon 5 Lectin 20301226, 19937244, 20331761, 20664902, 21429375, 20231421, Lys302X Exon 8 10090935, 10090934 Gln317X Exon 8 17910641 Glu321X Exon 9 16304051 Gln380X Exon 9 16676083 Arg456X Exon 11 10090934, 15876275 Splice site Mutation Codon Exon/Intron Domain PMID IVS1-1 G>C Intron 1 16304051 IVS2+5 G>A Intron 2 16304051, 18391077 149+5G>A Intron 2 17610559 IVS3+1G>A Intron 3 EF1 12717434 IVS5+1G>T Intron 5 Lectin 10090934 822G>A Exon 7 Lectin 10090934 IVS7+1G>A Intron 7 Lectin 16304051 IVS7+33insGGTT Intron 7 Lectin 16304051 IVS7-1G>C Intron 7 Lectin 15876275 IVS9+2T>G Exon 9 10090934 IVS9+2T>C Exon 9 10090935, 18391077 * The positions are based on the protein sequence inclusive of the signal peptide if present.
Home > Mutations
The mutations reported for Combined Factor V and VIII deficiency are listed below:
Missense
Insertion
Deletion
Nonsense
Splice site
* The positions are based on the protein sequence inclusive of the signal peptide if present.
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