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Search Results: 2 unique variants retrieved
p.Cys151Arg (Legacy AA No. 91)
Variant Type:
Point
Domain:
EGF2
Sequence Context:
CGT > TGT
Variant Effect:
Missense
Location:
Exon (6)
No of bases:
1
No. of patients reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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Patient Information : Show
p.Cys151Ser (Legacy AA No. 91)
Variant Type:
Point
Domain:
EGF2
Sequence Context:
TGT > TCT
Variant Effect:
Missense
Location:
Exon (6)
No of bases:
1
No. of patients reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Please click
here
to see if there is the available information.