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


  c.6362T>A
p.(Ile2121Asn) (Legacy AA No.2102)
Variant Type:
Point
Domain:
C1
Sequence Context:
ATC > AAC
Variant Effect:
Missense
Location:
Exon 22
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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