In Depth Variant Analysis: c.796G>A (p.Ala266Thr)
c.796G>A
p.Ala266Thr (Legacy AA No. 206)
Mutation Type:
Point
Domain:
Serine Protease
Codon Change:
GCG > ACG
Mutation Effect:
Missense
Location:
Exon(8)
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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