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
Screenings
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