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  Search Results: 2 unique variants retrieved




  c.26C>G
p.Ala9Gly (-38)
Mutation Type:
Point
Domain:
Signal Peptide
Nucleotide number:
55
Mutation Effect:
Missense
Location:
Exon(1)
CpG:
-
No. of patients reported:
1
No. of bases:
1

Structural Information

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Patient Information : Show

  c.26C>G
p.Ala9Gly (-37)
Mutation Type:
Polymorphism
Domain:
Signal Peptide
Nucleotide number:
55
Mutation Effect:
Missense
Location:
Exon(1)
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