Variant #0000985260 (NC_000003.11:g.38802682C>T, NC_000003.11(NM_006514.2):c.883+1G>A (SCN10A))
| Chromosome |
3 |
| 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.38802682C>T |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SCN10A_000326 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs757136675 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2024-05-15 10:34:01 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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