Variant #0000974421 (NC_000002.11:g.166898844G>A, NM_001165963.1:c.2134C>T (SCN1A))
Chromosome |
2 |
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.166898844G>A |
DNA change (hg38) |
- |
Published as |
SCN1A(NM_001165963.4):c.2134C>T (p.R712*) |
ISCN |
- |
DB-ID |
SCN1A_000296 See all 5 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2024-04-19 20:20:39 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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