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

  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



  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