Home Query References Browse Contact
Mutation Query
Allele 1:A467T
Allele 2: A957P

Allelic information known

Refine query
467957
Residue A467
Cluster assignment:
Cluster 2
Cluster description:Upstream DNA binding channel
Subcluster:2A (residues 463-468)
Subcluster description:Subcluster 2A maps to a region of the thumb subdomain of the pol domain at the accessory subunit interface where A467T, N468D and L463F are positioned.
POLG domain:Polymerase domain
Residue A957
Cluster assignment:
Cluster 1
Cluster description:Polymerase active site and environs
Subcluster:1E (residues 914-966)
Subcluster description:This subcluster comprises most of the fingers subdomain of the pol domain, including the O-helix and the Pol B motif (Loh and Loeb, 2005).
POLG domain:Polymerase domain
Mutation Information
A467T
Number of patients:

(with A467T)

236
Found as the only mutation:3% of entries (6 patients)
Found together with:
Non-allelic
19
A467T
19
W748S
10
G848S
8
PNF
7
E1143G
6
T914P
3
G303R
3
R852C
2
L304R
2
L966R
%
Also:
T251I (1%) P587L (1%) S305R (1%)
G11D (1%) A957P (1%) R627W (1%)
R574W (1%) F749S (1%) R227P (1%)
C418R (1%) P1073L (1%) C1188R (1%)
G737R (1%) R1138C (1%) R627Q (1%)
Q1236H (1%) R232H (1%) H277L (1%)
R3P (1%) F88L (0%) A143V (0%)
R227W (0%) R417T (0%) L428P (0%)
S1095R (0%) R807C (0%) R807H (0%)
L886P (0%) K1191N (0%) L605R (0%)
G588D (0%) H754Q (0%) R597W (0%)
L1113P (0%) P625R (0%) S1104C (0%)
G268A (0%) R275Q (0%) R1096C (0%)
K561M (0%) Q879H (0%) M919T (0%)
S1104F (0%) Q497H (0%)
Allelic
1
PNF
0
T885S
%

PNF=Putatively Non-Functional enzyme

Show Patient Data
A957P
Number of patients:

(with A957P)

3
Non-allelic with:A467T (100%)
Show Patient Data
Database patient data is inconclusive about the dominant status of mutation A467T.

See full list of putatively-dominant POLG mutations

The following information is based on existing patient data and pathogenic cluster assignment.

Pathogenicity information for a patient with mutation A467T and a cluster 1 mutation:
Age of onset information is extracted from a total of 66 patients and/ or patient families.
Age of onset
66-
33-
50
9
1
6
infantilechildhdjuvenileadult
76%14%2%9%
All mutations mapping within the pathogenic clusters are at high risk for pathogenicity. In general, a patient must have a pathogenic mutation in both of his/ her POLG genes to develop a POLG-related syndrome.
Symptoms described in patients with A467T-cluster1 mutations
Symptoms described in patients with cluster2-cluster1 mutations
New Mutation Query
Type in POLG mutations:
Allele 1:Allele 2:
Allelic information known
Allelic information not known
Example input: A467T T914P
Mutations in the same allele can be separated with a comma
:.: Privacy Statement :.: Disclaimer :.: Contact Information :.: