Search Results: 2 unique variants retrieved
c.3984dupA
p.(Arg1329Thrfs*1) (Legacy AA No.1310)
Variant Type:
Duplication
Domain:
B
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 14
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 (Duplication | Frameshift) of mutation at Exon 14
Individual Case Information :
Show
c.3986G>A
p.(Arg1329His) (Legacy AA No.1310)
Variant Type:
Point
Domain:
B
Sequence Context:
CGT > CAT
Variant Effect:
Missense
Location:
Exon 14
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show