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  Search Results: 2 unique variants retrieved



  c.6769A>G
p.(Met2257Val) (Legacy AA No.2238)
Variant Type:
Point
Domain:
C2
Sequence Context:
ATG > GTG
Variant Effect:
Missense
Location:
Exon 25
No of bases:
1
No. of cases reported:
6
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show


  c.6769A>G
p.(Met2257Val) (Legacy AA No.2238)
Variant Type:
Polymorphism
Domain:
C2
Sequence Context:
ATG > GTG
Variant Effect:
Non-Synonymous
Location:
Exon 25
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Structural Analysis cannot be performed for this type (Polymorphism | Non-Synonymous) of mutation at Exon 25

Individual Case Information : Show