EAHAD Factor VIII Variant Database
Data Display Options:
UNIQUE (Without Case Data) :
MULTIPLE (With Case Data) :



Search Results: 1 unique variant retrieved.


  c.7001A>C
p.(His2334Pro) (Legacy AA No.2315)
Variant Type:
Point
Domain:
C2
Sequence Context:
CAC > CCC
Variant Effect:
Missense
Location:
Exon 26
No of bases:
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