In-Depth Variant Analysis:  c.198G>C (p.Glu66Asp)
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c.198G>C
p.Glu66Asp (Legacy AA No. 26)
Variant Type: 
Point
Domain: 
Gla domain
Location: 
Exon 2
Variant Effect: 
Missense
Codon Change: 
G>C
No. of Patients Reported: 
0
Phenotype: 
U
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-
Variant Comments & Reference:
Residue Information:
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Substitution Analysis:
Structural Implications:
Glu66 is an exposed residue  (surface accessibility value = 2 ).
Glu66 is in a region of secondary structure within the FX domains.
The DSSP assignment for this residue is ... H.
Glu66 is in a region of secondary structure within the FX domains.
The DSSP assignment for this residue is ... H.
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