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: 2 unique variants retrieved


Variant No. 401
p.(Glu620Arg) Legacy AA No. 602
Variant Type:
Indel
Genomic:
27631_27632delinsAG
Domain:
Serine Protease
Codon Change:
GAG > AGG
Variant Effect:
Missense
Location:
Exon (15)
No of bases:
2
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. 402
p.(Glu620Gln) Legacy AA No. 602
Variant Type:
Point
Genomic:
27631G>C
Domain:
Serine Protease
Codon Change:
GAG > CAG
Variant Effect:
Missense
Location:
Exon (15)
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