Variant #0000016743 (NC_000007.13:g.107423522C>G, NM_000111.2:c.1136G>C (SLC26A3))
| Chromosome |
7 |
| Allele |
Unknown |
| 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.107423522C>G |
| DNA change (hg38) |
g.107783077C>G |
| Published as |
c.1136G>C |
| ISCN |
- |
| DB-ID |
SLC26A3_000023 See all 2 reported entries |
| Variant remarks |
1 British DIAR1 patient |
| Reference |
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) |
2.0E-5 View details |
| 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 |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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