Variant #0000655411 (NC_000005.9:g.74981146G>A, NM_001099271.1:c.1293C>T (POC5))
| Chromosome |
5 |
| 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.74981146G>A |
| DNA change (hg38) |
g.75685321G>A |
| Published as |
POC5(NM_001099271.1):c.1293C>T (p.A431=) |
| ISCN |
- |
| DB-ID |
POC5_000003 |
| 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
|