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  Search Results: 2 unique variants retrieved



  c.241G>T
p.(Ala81Ser) (Legacy AA No.62)
Variant Type:
Point
Domain:
A1
Sequence Context:
GCT > TCT
Variant Effect:
Missense
Location:
Exon 2
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.242C>A
p.(Ala81Asp) (Legacy AA No.62)
Variant Type:
Point
Domain:
A1
Sequence Context:
GCT > GAT
Variant Effect:
Missense
Location:
Exon 2
No of bases:
1
No. of cases reported:
7
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show