EAHAD Factor VIII Variant Database
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Search Results: 2 unique variants retrieved


  c.6082G>T
p.(Gly2028Trp ) (Legacy AA No.2009)
Variant Type:
Point
Domain:
A3
Sequence Context:
GGG > TGG
Variant Effect:
Missense
Location:
Exon 19
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.6082G>A
p.(Gly2028Arg) (Legacy AA No.2009)
Variant Type:
Point
Domain:
A3
Sequence Context:
GGG > AGG
Variant Effect:
Missense
Location:
Exon 19
No of bases:
1
No. of cases reported:
10
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Please click to see if there is the available information.
Individual Case Information : Show