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  Search Results: 3 unique variants retrieved



  c.1744G>A
p.(Gly582Arg) (Legacy AA No.563)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGA > AGA
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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  c.1745G>C
p.(Gly582Ala) (Legacy AA No.563)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGA > GCA
Variant Effect:
Missense
Location:
Exon 11
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.1745G>A
p.(Gly582Glu) (Legacy AA No.563)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGA > GAA
Variant Effect:
Missense
Location:
Exon 11
No of bases:
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