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  Search Results: 3 unique variants retrieved



  c.823C>A
p.(His275Asn) (Legacy AA No.256)
Variant Type:
Point
Domain:
A1
Sequence Context:
CAT > AAT
Variant Effect:
Missense
Location:
Exon 7
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.824A>G
p.(His275Arg) (Legacy AA No.256)
Variant Type:
Point
Domain:
A1
Sequence Context:
CAT > CGT
Variant Effect:
Missense
Location:
Exon 7
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.824A>T
p.(His275Leu) (Legacy AA No.256)
Variant Type:
Point
Domain:
A1
Sequence Context:
CAT > CTT
Variant Effect:
Missense
Location:
Exon 7
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