Variant #0000350412 (NC_000012.11:g.52082871G>A, NC_000012.11(NM_014191.3):c.706+238G>A (SCN8A))
| Chromosome |
12 |
| 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.52082871G>A |
| DNA change (hg38) |
g.51689087G>A |
| Published as |
SCN8A(NM_001330260.2):c.697G>A (p.V233I) |
| ISCN |
- |
| DB-ID |
SCN8A_000068 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) |
Retrieve |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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