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  Search Results: 3 unique variants retrieved



  c.301G>C
p.(Asp101His) (Legacy AA No.82)
Variant Type:
Point
Domain:
A1
Sequence Context:
GAT > CAT
Variant Effect:
Missense
Location:
Exon 3
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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  c.302A>G
p.(Asp101Gly) (Legacy AA No.82)
Variant Type:
Point
Domain:
A1
Sequence Context:
GAT > GGT
Variant Effect:
Missense
Location:
Exon 3
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


  c.302A>T
p.(Asp101Val) (Legacy AA No.82)
Variant Type:
Point
Domain:
A1
Sequence Context:
GAT > GTT
Variant Effect:
Missense
Location:
Exon 3
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show