Variant #0000857810 (NC_000002.11:g.166032639A>C, NM_021007.2:c.-118058A>C (SCN2A))
| Chromosome |
2 |
| 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.166032639A>C |
| DNA change (hg38) |
- |
| Published as |
SCN3A(NM_001081676.1):c.264+2T>G (p.?) |
| ISCN |
- |
| DB-ID |
SCN2A_000308 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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