Variant #0000725655 (NC_000016.9:g.23226701G>A, NM_001039.3:c.1861G>A (SCNN1G))
Chromosome |
16 |
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.23226701G>A |
DNA change (hg38) |
- |
Published as |
SCNN1G(NM_001039.3):c.1861G>A (p.G621S) |
ISCN |
- |
DB-ID |
SCNN1G_000026 |
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) |
6.0E-5 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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