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  Search Results: 4 unique variants retrieved



  c.5881T>A
p.(Trp1961Arg) (Legacy AA No.1942)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > AGG
Variant Effect:
Missense
Location:
Exon 18
No of bases:
1
No. of cases reported:
4
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.5881T>C
p.(Trp1961Arg) (Legacy AA No.1942)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > CGG
Variant Effect:
Missense
Location:
Exon 18
No of bases:
1
No. of cases reported:
4
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.5882G>A
p.(Trp1961*) (Legacy AA No.1942)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > TAG
Variant Effect:
Nonsense
Location:
Exon 18
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 18

Individual Case Information : Show


  c.5883G>A
p.(Trp1961*) (Legacy AA No.1942)
Variant Type:
Point
Domain:
A3
Sequence Context:
TGG > TGA
Variant Effect:
Nonsense
Location:
Exon 18
No of bases:
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 18

Individual Case Information : Show