Search Results: 2 unique variants retrieved
c.1338delA
p.(Phe447Leufs*35) (Legacy AA No.428)
Variant Type:
Deletion
Domain:
A2
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 9
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Deletion | Frameshift) of mutation at Exon 9
Individual Case Information :
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c.1340T>C
p.(Phe447Ser) (Legacy AA No.428)
Variant Type:
Point
Domain:
A2
Sequence Context:
TTT > TCT
Variant Effect:
Missense
Location:
Exon 9
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show