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  Search Results: 1 unique variant retrieved.




  c.10G>A
p.Val4Met (-42)
Mutation Type:
Polymorphism
Domain:
Signal Peptide
Nucleotide number:
39
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


Factor IX Variant Database