In Depth Mutation Analysis: c.51C>G (p.Ile17Met)
c.51C>G
p.Ile17Met (-29)
Mutation Type:
Polymorphism
Mutation Effect:
Missense
Domain:
Signal Peptide
Location:
Exon 1
No. of bases:
1
CpG:
N
Comments:
dbSNP database
No. of patients reported:
1
Patient Information : Show
Residue Information :
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Structural Implications :
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