Variant #0000044719 (NC_000019.9:g.35524817_35524818del, NM_199037.3:c.622_623del (SCN1B))
| Chromosome |
19 |
| 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.35524817_35524818del |
| DNA change (hg38) |
g.35033913_35033914del |
| Published as |
delCT |
| ISCN |
- |
| DB-ID |
SCN1B_000003 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Uschi Peeters |
| Database submission license |
No license selected |
| Created by |
Uschi Peeters |
| Date created |
2014-10-10 14:01:08 +02:00 (CEST) |
| Date last edited |
2014-10-11 13:06:24 +02:00 (CEST) |

Variant on transcripts
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