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  Search Results: 3 unique variants retrieved



  c.5641_5642delACinsGA
p.(Thr1881Glu) (Legacy AA No.1862)
Variant Type:
Indel
Domain:
A3
Sequence Context:
Variant Effect:
Inframe
Location:
Exon 17
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 (Indel | Inframe) of mutation at Exon 17

Individual Case Information : Show


  c.5641delA
p.(Thr1881Hisfs*2) (Legacy AA No.1862)
Variant Type:
Deletion
Domain:
A3
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 17
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 17

Individual Case Information : Show


  c.5641A>C
p.(Thr1881Pro) (Legacy AA No.1862)
Variant Type:
Point
Domain:
A3
Sequence Context:
ACA > CCA
Variant Effect:
Missense
Location:
Exon 17
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show