Variant #0000000592 (NC_000008.10:g.30921954G>C, NC_000008.10(NM_000553.4):c.355+4G>C (WRN))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Probably does not affect function |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.30921954G>C |
| Reference |
- |
| DB-ID |
WRN_000001 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00155 View details |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2024-06-03 15:55:36 +00:00 (UTC) |
| Date last edited |
N/A |

Variant on transcripts
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