Transcript #00028421 (NM_001184741.1, FGB gene)

Transcript name transcript variant 2
Gene name FGB (fibrinogen beta chain)
Chromosome 4
Transcript - NCBI ID NM_001184741.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001171670.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

43 entries on 1 page. Showing entries 1 - 43.
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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.166-25T>C 166 r.(=) p.(=) - intron 25
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.390C>T 390 r.(?) p.(=) - coding-synonymous -
./. - c.666G>T 666 r.(?) p.(=) - coding-synonymous -
./. - c.666G>T 666 r.(?) p.(=) - coding-synonymous -
./. - c.684C>T 684 r.(?) p.(=) - coding-synonymous -
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.782-16_782-13del 782 r.(=) p.(=) - intron 13
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.948C>T 948 r.(?) p.(=) - coding-synonymous -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
./. - c.1256G>A 1256 r.(?) p.(Arg419Lys) - missense -
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