Variant #0000323622 (NC_000014.8:g.24653972G>A, NC_000014.8(NM_024658.3):c.1523-3C>T (IPO4))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24653972G>A |
| DNA change (hg38) |
g.24184766G>A |
| Published as |
IPO4(NM_024658.3):c.1523-3C>T (p.?) |
| ISCN |
- |
| DB-ID |
IPO4_000001 |
| 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) |
0.00122 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 |
2020-07-05 13:45:10 +02:00 (CEST) |

Variant on transcripts
|