Variant #0000910722 (NC_000001.10:g.10042688G>A, NM_022787.3:c.769G>A (NMNAT1))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.10042688G>A |
DNA change (hg38) |
- |
Published as |
NMNAT1(NM_001297778.1):c.769G>A (p.E257K), NMNAT1(NM_022787.3):c.769G>A (p.E257K, p.(Glu257Lys)) |
ISCN |
- |
DB-ID |
NMNAT1_000002 See all 108 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) |
0.0007 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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