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  Search Results: 2 unique variants retrieved



  c.1699A>T
p.(Ile567Phe) (Legacy AA No.548)
Variant Type:
Point
Domain:
A2
Sequence Context:
ATT > TTT
Variant Effect:
Missense
Location:
Exon 11
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


  c.1700T>C
p.(Ile567Thr) (Legacy AA No.548)
Variant Type:
Point
Domain:
A2
Sequence Context:
ATT > ACT
Variant Effect:
Missense
Location:
Exon 11
No of bases:
1
No. of cases reported:
13
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show