Variant #0000324278 (NC_000015.9:g.89873415G>A, NM_002693.2:c.752C>T (POLG))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89873415G>A |
DNA change (hg38) |
g.89330184G>A |
Published as |
POLG(NM_001126131.2):c.752C>T (p.T251I), POLG(NM_002693.2):c.752C>T (p.T251I), POLG(NM_002693.3):c.752C>T (p.(Thr251Ile), p.T251I) |
ISCN |
- |
DB-ID |
POLG_000194 See all 6 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00153 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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