POLG Pathogenicity Prediction Server
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Type in
POLG
mutations:
Allele 1:
Allele 2:
All mutations:
Allelic information known
Allelic information
not
known
Example input:
A467T
T914P
Example input:
A467T, T914P
Mutations in the same allele can be separated with a comma
Separate mutations by commas
PNF mutation queries are not supported, please use the
patient data search
where PNF queries are supported.
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Mutations outside assigned pathogenic clusters are considered to be SNPs (single nucleotide polymorphisms).