Search Results: 5 unique variants retrieved
c.1237G>T
p.(Gly413*) (367)
Variant Type:
Point
Domain:
Serine Protease
cDNA number:
1237
Variant Effect:
Nonsense
Location:
Exon(8)
CpG:
N
No. of cases reported:
1
No. of bases:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis is only available for missense variants and cannot be performed for this type (Point | Nonsense) of variant at Exon 8.
Individual Case Information :
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c.1237G>C
p.(Gly413Arg) (367)
Variant Type:
Point
Domain:
Serine Protease
cDNA number:
1237
Variant Effect:
Missense
Location:
Exon(8)
CpG:
No. of cases reported:
2
No. of bases:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.1237G>A
p.(Gly413Arg) (367)
Variant Type:
Point
Domain:
Serine Protease
cDNA number:
1237
Variant Effect:
Missense
Location:
Exon(8)
CpG:
N
No. of cases reported:
7
No. of bases:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.1238G>C
p.(Gly413Ala) (367)
Variant Type:
Point
Domain:
Serine Protease
cDNA number:
1238
Variant Effect:
Missense
Location:
Exon(8)
CpG:
N
No. of cases reported:
1
No. of bases:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.1238G>A
p.(Gly413Glu) (367)
Variant Type:
Point
Domain:
Serine Protease
cDNA number:
1238
Variant Effect:
Missense
Location:
Exon(8)
CpG:
N
No. of cases reported:
3
No. of bases:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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