EAHAD Factor VIII Variant Database
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Search Results: 1 unique variant retrieved.


  c.5093T>C
p.(Ile1698Thr) (Legacy AA No.1679)
Variant Type:
Point
Domain:
a3
Sequence Context:
ATT > ACT
Variant Effect:
Missense
Location:
Exon 14
No of bases:
1
No. of cases reported:
8
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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