Variant #0000016744 (NC_000007.13:g.107423510_107423511del, NM_000111.2:c.1148_1149del (SLC26A3))
| Chromosome |
7 |
| Allele |
Paternal (confirmed) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.107423510_107423511del |
| DNA change (hg38) |
g.107783065_107783066del |
| Published as |
deletion at 1148–1149 of a TA dinucleotide: frameshift, truncated protein product 455 amino acids long |
| ISCN |
- |
| DB-ID |
SLC26A3_000080 |
| Variant remarks |
2 Andalusian (southern Spain) sibs (com-het) and 1 Spanish DIAR1 patient |
| Reference |
PubMed: Rodriques-Herrera et al. 2011, PubMed: Wedenoja et al. 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-10 17:16:02 +01:00 (CET) |
| Date last edited |
2020-06-23 13:23:32 +02:00 (CEST) |

Variant on transcripts
|