Data Display Options:
UNIQUE (Without Case Data) :
MULTIPLE (With Case Data) :



REFERENCE SEARCH: click one of the four options above to download or display variants/cases from your chosen publication.


Search Results: 3 unique variants retrieved


Variant No. 289
p.(Trp425Arg) Legacy AA No. 407
Variant Type:
Point
Genomic:
23266T>A
Domain:
Serine Protease
Codon Change:
TGG > AGG
Variant Effect:
Missense
Location:
Exon (11)
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show

Variant No. 290
p.(Trp425Leu) Legacy AA No. 407
Variant Type:
Point
Genomic:
23267G>T
Domain:
Serine Protease
Codon Change:
TGG > TTG
Variant Effect:
Missense
Location:
Exon (11)
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show

Variant No. 291
p.(Trp425Cys) Legacy AA No. 407
Variant Type:
Point
Genomic:
23268G>C
Domain:
Serine Protease
Codon Change:
TGG > TGC
Variant Effect:
Missense
Location:
Exon (11)
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show