EAHAD Factor VIII Variant Database
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Search Results: 4 unique variants retrieved


  c.5560T>G
p.(Trp1854Gly) (Legacy AA No.1835)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > GGG
Variant Effect:
Missense
Location:
Exon 16
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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Individual Case Information : Show

  c.5561G>A
p.(Trp1854*) (Legacy AA No.1835)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > TAG
Variant Effect:
Nonsense
Location:
Exon 16
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 16
Individual Case Information : Show

  c.5562G>A
p.(Trp1854*) (Legacy AA No.1835)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > TGA
Variant Effect:
Nonsense
Location:
Exon 16
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 16
Individual Case Information : Show

  c.5562G>T
p.(Trp1854Cys) (Legacy AA No.1835)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > TGT
Variant Effect:
Missense
Location:
Exon 16
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Please click to see if there is the available information.
Individual Case Information : Show