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  Search Results: 2 unique variants retrieved



  c.5932A>G
p.(Ser1978Gly) (Legacy AA No.1959)
Variant Type:
Point
Domain:
A3
Sequence Context:
AGT > GGT
Variant Effect:
Missense
Location:
Exon 18
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.5934T>G
p.(Ser1978Arg) (Legacy AA No.1959)
Variant Type:
Point
Domain:
A3
Sequence Context:
AGT > AGG
Variant Effect:
Missense
Location:
Exon 18
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