In-Depth Variant Analysis:  c.2129A>G (p.His710Arg)
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c.2129A>G
p.His710Arg (Legacy AA No. 682)
Variant Type: 
Point
Domain: 
d5a2
Location: 
Exon 13
Variant Effect: 
Missense
Codon Change: 
2129A>G
No. of Patients Reported: 
1
Phenotype: 
NA
Allele Count *: 
285
Allele Number *: 
282458
Allele Frequency *: 
0.001009
Variant Comments & Reference:
NAResidue Information:
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Substitution Analysis:
Structural Implications:
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