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Search Results: 2 unique variants retrieved
c.22A>G
p.Met8Val (-38)
Mutation Type:
Polymorphism
Domain:
Signal Peptide
Nucleotide number:
51
Mutation Effect:
Missense
Location:
Exon(1)
CpG:
N
No. of patients reported:
1
No. of bases:
1
Structural Information
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to show detailed structural analysis of this mutation.
Patient Information : Show
c.23T>C
p.Met8Thr (-38)
Mutation Type:
Polymorphism
Domain:
Signal Peptide
Nucleotide number:
52
Mutation Effect:
Missense
Location:
Exon(1)
CpG:
N
No. of patients reported:
1
No. of bases:
1
Structural Information
Please click
here
to show detailed structural analysis of this mutation.