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  Search Results: 3 unique variants retrieved



  c.5386A>G
p.(Asn1796Asp) (Legacy AA No.1777)
Variant Type:
Point
Domain:
A3
Sequence Context:
AAT > GAT
Variant Effect:
Missense
Location:
Exon 16
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.5387delA
p.(Asn1796Ilefs*75) (Legacy AA No.1777)
Variant Type:
Deletion
Domain:
A3
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 16
No of bases:
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 16

Individual Case Information : Show


  c.5387A>G
p.(Asn1796Ser) (Legacy AA No.1777)
Variant Type:
Point
Domain:
A3
Sequence Context:
AAT > AGT
Variant Effect:
Missense
Location:
Exon 16
No of bases:
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show