Variant #0000606024 (NC_000001.10:g.979397G>A, NM_198576.3:c.1993G>A (AGRN))
| Chromosome |
1 |
| 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.979397G>A |
| DNA change (hg38) |
g.1044017G>A |
| Published as |
AGRN(NM_001305275.2):c.1993G>A (p.E665K), AGRN(NM_198576.3):c.1993G>A (p.(Glu665Lys)) |
| ISCN |
- |
| DB-ID |
AGRN_000054 See all 2 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) |
0.00282 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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