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  Search Results: 2 unique variants retrieved



  c.6352T>C
p.(Ser2118Pro) (Legacy AA No.2099)
Variant Type:
Point
Domain:
C1
Sequence Context:
TCT > CCT
Variant Effect:
Missense
Location:
Exon 22
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.6353C>T
p.(Ser2118Phe) (Legacy AA No.2099)
Variant Type:
Point
Domain:
C1
Sequence Context:
TCT > TTT
Variant Effect:
Missense
Location:
Exon 22
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