Variant #0000016756 (NC_000007.13:g.107434303_107434315del, NM_000111.2:c.145_157del (SLC26A3))
| Chromosome |
7 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.107434303_107434315del |
| DNA change (hg38) |
g.107793858_107793870del |
| Published as |
c.145-157del13bp |
| ISCN |
- |
| DB-ID |
SLC26A3_000001 See all 3 reported entries |
| Variant remarks |
2 Belgian siblings (Togo ancestry; hom) with DIAR1 |
| Reference |
PubMed: Makela et al. 2002 |
| 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 13:23:57 +02:00 (CEST) |

Variant on transcripts
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