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  Search Results: 2 unique variants retrieved



  c.1657T>C
p.(Ser553Pro) (Legacy AA No.534)
Variant Type:
Point
Domain:
A2
Sequence Context:
TCT > CCT
Variant Effect:
Missense
Location:
Exon 11
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.1658C>G
p.(Ser553Cys) (Legacy AA No.534)
Variant Type:
Point
Domain:
A2
Sequence Context:
TCT > TGT
Variant Effect:
Missense
Location:
Exon 11
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