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  Search Results: 2 unique variants retrieved



  c.1634C>G
p.(Pro545Arg) (Legacy AA No.526)
Variant Type:
Point
Domain:
A2
Sequence Context:
CCT > CGT
Variant Effect:
Missense
Location:
Exon 11
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.1634C>A
p.(Pro545His) (Legacy AA No.526)
Variant Type:
Point
Domain:
A2
Sequence Context:
CCT > CAT
Variant Effect:
Missense
Location:
Exon 11
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