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  Search Results: 2 unique variants retrieved



  c.1957G>A
p.(Val653Met) (Legacy AA No.634)
Variant Type:
Point
Domain:
A2
Sequence Context:
GTG > ATG
Variant Effect:
Missense
Location:
Exon 13
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.1958T>C
p.(Val653Ala) (Legacy AA No.634)
Variant Type:
Point
Domain:
A2
Sequence Context:
GTG > GCG
Variant Effect:
Missense
Location:
Exon 13
No of bases:
1
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