In Depth Variant Analysis: c.1087C>A (p.Pro363Thr)
c.1087C>A
p.Pro363Thr (Legacy AA No. 303)
Mutation Type:
Point
Domain:
Serine Protease
Codon Change:
CCC > ACC
Mutation Effect:
Missense
Location:
Exon(9)
No of bases:
1
No. of patients reported:
2
Patient Information : Show
Residue Information :
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Substitution Analysis :
Structural Implications :
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