Variant #0000867289 (NC_000023.10:g.24745161C>T, NM_016937.3:c.1486C>T (POLA1))
| Chromosome |
X |
| 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.24745161C>T |
| DNA change (hg38) |
- |
| Published as |
POLA1(NM_001330360.2):c.1504C>T (p.(Pro496Ser)), POLA1(NM_016937.3):c.1486C>T (p.P496S), POLA1(NM_016937.4):c.1486C>T (p.P496S) |
| ISCN |
- |
| DB-ID |
POLA1_000019 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) |
0.00052 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|