Variant #0000016481 (NC_000005.9:g.149360062_149360063del, NM_000112.3:c.906_907del (SLC26A2))
| Chromosome |
5 |
| Allele |
Unknown |
| 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.149360062_149360063del |
| DNA change (hg38) |
g.149980499_149980500del |
| Published as |
933-934delCT: FS/stop |
| ISCN |
- |
| DB-ID |
SLC26A2_000016 |
| Variant remarks |
Rare French DTD mutation |
| Reference |
PubMed: Rossi et al. 2001 |
| 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 |
2012-11-15 14:17:13 +01:00 (CET) |
| Date last edited |
2020-06-18 08:52:09 +02:00 (CEST) |

Variant on transcripts
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