Variant #0000556105 (NC_000015.9:g.89876867_89876869dup, NM_002693.2:c.125_127dup (POLG))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89876867_89876869dup |
| DNA change (hg38) |
g.89333636_89333638dup |
| Published as |
POLG(NM_002693.2):c.125_127dupGGC (p.(Arg42dup)), POLG(NM_002693.2):c.125_127dupGGC (p.R42dup), POLG(NM_002693.3):c.125_127dupGGC (p.R42dup) |
| ISCN |
- |
| DB-ID |
POLG_000180 See all 3 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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