Variant #0000933851 (NC_000016.9:g.56900547_56900598dup, NC_000016.9(NM_000339.2):c.283-438_283-387dup (SLC12A3))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56900547_56900598dup |
DNA change (hg38) |
g.56866635_56866686dup |
Published as |
- |
ISCN |
- |
DB-ID |
SLC12A3_000197 See all 2 reported entries |
Variant remarks |
in vitro midigene splicing assay; suggested clinical classification variant “likely pathogenic" |
Reference |
PubMed: Viering 2023, Journal: Viering 2023 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-10-06 17:19:51 +02:00 (CEST) |
Date last edited |
2023-10-12 14:34:16 +02:00 (CEST) |

Variant on transcripts
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