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Search Results: 2 unique variants retrieved


Variant No. 278
p.(Thr407Ala) Legacy AA No. 389
Variant Type:
Point
Genomic:
23212A>G
Domain:
Serine Protease
Codon Change:
ACA > GCA
Variant Effect:
Missense
Location:
Exon (11)
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show

Variant No. 277
p.(Thr407Pro) Legacy AA No. 389
Variant Type:
Point
Genomic:
23212A>C
Domain:
Serine Protease
Codon Change:
ACA > CCA
Variant Effect:
Missense
Location:
Exon (11)
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show