Data Export Options:
Search Results: 2 unique variants retrieved
p.Gly22Ser (Legacy AA No. -39)
Variant Type:
Point
Domain:
Propeptide
Sequence Context:
GGC > AGC
Variant Effect:
Missense
Location:
Exon (1)
No of bases:
1
No. of patients reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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Patient Information : Show
p.Gly22Gly (Legacy AA No. -38)
Variant Type:
Point
Domain:
Propeptide
Sequence Context:
GGT > GGC
Variant Effect:
Missense
Location:
Exon (1)
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.