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  Search Results: 3 unique variants retrieved




  c.211T>C
p.Phe71Leu (25)
Mutation Type:
Polymorphism
Domain:
Gla
Nucleotide number:
6448
Mutation Effect:
Missense
Location:
Exon(2)
CpG:
N
No. of patients reported:
1
No. of bases:
1

Structural Information

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Patient Information : Show

  c.212T>C
p.Phe71Ser (25)
Mutation Type:
Point
Domain:
Gla
Nucleotide number:
6449
Mutation Effect:
Missense
Location:
Exon(2)
CpG:
N
No. of patients reported:
6
No. of bases:
1

Structural Information

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Patient Information : Show

  c.212T>G
p.Phe71Cys (25)
Mutation Type:
Point
Domain:
Gla
Nucleotide number:
6449
Mutation Effect:
Missense
Location:
Exon(2)
CpG:
N
No. of patients reported:
1
No. of bases:
1

Structural Information

Please click here to show detailed structural analysis of this mutation.

Patient Information : Show


Factor IX Variant Database