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Search Results: 2 unique variants retrieved


Variant No. 392
p.(Val611Met) (Legacy AA No. 593)
Variant Type:
Point
Genomic:
27604G>A
Codon Change:
GTG ATG
Variant Effect:
Missense
Location:
Exon 15
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Domain:
Serine Protease
Pathogenicity(ACMG): 2=Likely Benign, 3=Uncertain, 4=Likely Pathogenic:

Individual Case Information : Show


Variant No. 393
p.(Val611Gly) (Legacy AA No. 593)
Variant Type:
Point
Genomic:
27605T>G
Codon Change:
GTG GGG
Variant Effect:
Missense
Location:
Exon 15
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Domain:
Serine Protease
Pathogenicity(ACMG): 2=Likely Benign, 3=Uncertain, 4=Likely Pathogenic:

Individual Case Information : Show