Variant #0000509813 (NC_000002.11:g.166152415C>T, NM_021007.2:c.82C>T (SCN2A))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.166152415C>T |
| DNA change (hg38) |
g.165295905C>T |
| Published as |
SCN2A(NM_001040142.1):c.82C>T (p.R28C, p.(Arg28Cys)), SCN2A(NM_021007.2):c.82C>T (p.R28C), SCN2A(NM_021007.3):c.82C>T (p.R28C) |
| ISCN |
- |
| DB-ID |
SCN2A_000038 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) |
0.00025 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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