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  Search Results: 2 unique variants retrieved



  c.940A>G
p.(Thr314Ala) (Legacy AA No.295)
Variant Type:
Point
Domain:
A1
Sequence Context:
ACT > GCT
Variant Effect:
Missense
Location:
Exon 7
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.941C>T
p.(Thr314Ile) (Legacy AA No.295)
Variant Type:
Point
Domain:
A1
Sequence Context:
ACT > ATT
Variant Effect:
Missense
Location:
Exon 7
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