Variant #0000044892 (NC_000011.9:g.118047358G>A, NM_004588.4:c.-212C>T (SCN2B))
Chromosome |
11 |
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.118047358G>A |
DNA change (hg38) |
g.118176643G>A |
Published as |
- |
ISCN |
- |
DB-ID |
SCN2B_000002 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 |
2014-10-17 10:31:24 +02:00 (CEST) |
Date last edited |
2014-10-31 19:24:17 +01:00 (CET) |

Variant on transcripts
Screenings
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