Variant #0000300015 (NC_000004.11:g.170477125G>A, NM_001199397.1:c.1388C>T (NEK1))
| Chromosome |
4 |
| 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.170477125G>A |
| DNA change (hg38) |
g.169555974G>A |
| Published as |
NEK1(NM_001199397.1):c.1388C>T (p.A463V, p.(Ala463Val)), NEK1(NM_001199397.3):c.1388C>T (p.A463V), NEK1(NM_012224.3):c.1388C>T (p.A463V) |
| ISCN |
- |
| DB-ID |
NEK1_000019 See all 6 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) |
0.03556 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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