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


  c.6559G>A
p.(Gly2187Ser) (Legacy AA No.2168)
Variant Type:
Point
Domain:
C1
Sequence Context:
GGC > AGC
Variant Effect:
Missense
Location:
Exon 23
No of bases:
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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Individual Case Information : Show

  c.6560G>A
p.(Gly2187Asp) (Legacy AA No.2168)
Variant Type:
Point
Domain:
C1
Sequence Context:
GGC > GAC
Variant Effect:
Missense
Location:
Exon 23
No of bases:
No. of cases reported:
3
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Please click to see if there is the available information.
Individual Case Information : Show