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


  c.4828G>T
p.(Ala1610Ser) (Legacy AA No.1591)
Variant Type:
Point
Domain:
B
Sequence Context:
GCT > TCT
Variant Effect:
Missense
Location:
Exon 14
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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Individual Case Information : Show