In Depth Variant Analysis: c.968T>G (p.Leu323Arg)
c.968T>G
p.Leu323Arg (Legacy AA No. 263)
Mutation Type:
Point
Domain:
Serine Protease
Codon Change:
CGG > CTG
Mutation Effect:
Missense
Location:
Exon(9)
No of bases:
1
No. of patients reported:
1
Patient Information : Show
Residue Information :
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Substitution Analysis :
Structural Implications :
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