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  Search Results: 2 unique variants retrieved



  c.6904T>G
p.(Phe2302Val) (Legacy AA No.2283)
Variant Type:
Point
Domain:
C2
Sequence Context:
TTT > GTT
Variant Effect:
Missense
Location:
Exon 26
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.6905T>C
p.(Phe2302Ser) (Legacy AA No.2283)
Variant Type:
Point
Domain:
C2
Sequence Context:
TTT > TCT
Variant Effect:
Missense
Location:
Exon 26
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