RF Logo The European Association for Haemophilia and Allied Disorders Factor VII Variant Database EAHAD Coagulation Variant Databases

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  Search Results: 1 unique variant retrieved.



  c.121G>T
p.(Gly41Cys) (Legacy AA No.22)
Variant Type:
Point
Domain:
A1
Sequence Context:
GGT > TGT
Variant Effect:
Missense
Location:
Exon 1
No of bases:
1
No. of cases reported:
5
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show