Variant #0000657176 (NC_000012.11:g.6457051dup, NM_001038.5:c.2004dup (SCNN1A))
| Chromosome |
12 |
| 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.6457051dup |
| DNA change (hg38) |
g.6347885dup |
| Published as |
SCNN1A(NM_001159576.1):c.2181dupG (p.P728Afs*62) |
| ISCN |
- |
| DB-ID |
LTBR_000006 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-02 12:28:35 +02:00 (CEST) |

Variant on transcripts
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