Search Results: 3 unique variants retrieved
c.60delA
p.(Gly21Aspfs*22) Legacy AA -26
Variant Type:
Deletion
Domain:
Signal Peptide
cDNA number:
60
Variant Effect:
Frameshift
Location:
Exon(1)
CpG:
N
No. of cases reported:
2
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 (Deletion | Frameshift) of variant at Exon 1.
Individual Case Information :
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c.61G>T
p.(Gly21*) Legacy AA -26
Variant Type:
Point
Domain:
Signal Peptide
cDNA number:
61
Variant Effect:
Nonsense
Location:
Exon(1)
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 1.
Individual Case Information :
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c.62G>T
p.(Gly21Val) Legacy AA -26
Variant Type:
Point
Domain:
Signal Peptide
cDNA number:
62
Variant Effect:
Missense
Location:
Exon(1)
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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