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  Search Results: 2 unique variants retrieved



  c.5557G>A
p.(Ala1853Thr) (Legacy AA No.1834)
Variant Type:
Point
Domain:
A3
Sequence Context:
GCC > ACC
Variant Effect:
Missense
Location:
Exon 16
No of bases:
1
No. of cases reported:
8
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.5558C>T
p.(Ala1853Val) (Legacy AA No.1834)
Variant Type:
Point
Domain:
A3
Sequence Context:
GCC > GTC
Variant Effect:
Missense
Location:
Exon 16
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show