Transcript #00028420 (NM_005141.4, FGB gene)

Transcript name transcript variant 1
Gene name FGB (fibrinogen beta chain)
Chromosome 4
Transcript - NCBI ID NM_005141.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005132.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

44 entries on 1 page. Showing entries 1 - 44.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.115-12C>T 115 r.(=) p.(=) - intron 12
./. - c.291C>T 291 r.(?) p.(=) - coding-synonymous -
./. - c.318T>C 318 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.567C>T 567 r.(?) p.(=) - coding-synonymous -
./. - c.843G>T 843 r.(?) p.(=) - coding-synonymous -
./. - c.843G>T 843 r.(?) p.(=) - coding-synonymous -
./. - c.861C>T 861 r.(?) p.(=) - coding-synonymous -
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.959-16_959-13del 959 r.(=) p.(=) - intron 13
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1125C>T 1125 r.(?) p.(=) - coding-synonymous -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
./. - c.1433G>A 1433 r.(?) p.(Arg478Lys) - missense -
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