Data Display Options:
Search Results: 2 unique variants retrieved
c.6748C>T
p.(Gln2250*) (Legacy AA No.2231)
Variant Type:
Point
Domain:
C2
Sequence Context:
CAA > TAA
Variant Effect:
Nonsense
Location:
Exon 25
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 25
Individual Case Information : Show
c.6750A>C
p.(Gln2250His) (Legacy AA No.2231)
Variant Type:
Point
Domain:
C2
Sequence Context:
CAA > CAC
Variant Effect:
Missense
Location:
Exon 25
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):