EAHAD Factor VIII Variant Database
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Factor VIII Gene (F8) Variant Database  

F8
Data Display Options:
UNIQUE (Without Case Data) :
EXCEL/CSV
SCREEN TABLE
MULTIPLE (With Case Data) :
EXCEL/CSV
SCREEN TABLE



Search Results: 3 unique variants retrieved

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  c.6481C>A
p.(Pro2161Thr) (Legacy AA No.2142)
Variant Type:
Point
Domain:
C1
Sequence Context:
CCT > ACT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
1
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

  c.6482C>A
p.(Pro2161His) (Legacy AA No.2142)
Variant Type:
Point
Domain:
C1
Sequence Context:
CCT > CAT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Please click to see if there is the available information.
Individual Case Information : Show

  c.6482C>T
p.(Pro2161Leu) (Legacy AA No.2142)
Variant Type:
Point
Domain:
C1
Sequence Context:
CCT > CTT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
1
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
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