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

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  Search Results: 2 unique variants retrieved



  c.6772A>T
p.(Lys2258*) (Legacy AA No.2239)
Variant Type:
Point
Domain:
C2
Sequence Context:
AAA > TAA
Variant Effect:
Nonsense
Location:
Exon 25
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 25

Individual Case Information : Show


  c.6772A>G
p.(Lys2258Glu) (Legacy AA No.2239)
Variant Type:
Point
Domain:
C2
Sequence Context:
AAA > GAA
Variant Effect:
Missense
Location:
Exon 25
No of bases:
No. of cases reported:
7
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show