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  Search Results: 3 unique variants retrieved



  c.2066T>G
p.(Leu689Arg) (Legacy AA No.670)
Variant Type:
Point
Domain:
A2
Sequence Context:
CTA > CGA
Variant Effect:
Missense
Location:
Exon 13
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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  c.2066T>C
p.(Leu689Pro) (Legacy AA No.670)
Variant Type:
Point
Domain:
A2
Sequence Context:
CTA > CCA
Variant Effect:
Missense
Location:
Exon 13
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.2067_2088del
p.(Leu689Leufs*26) (Legacy AA No.670)
Variant Type:
Deletion
Domain:
A2
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 13
No of bases:
22
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 13

Individual Case Information : Show