Variant #0000016486 (NC_000005.9:g.149360517A>C, NM_000112.3:c.1361A>C (SLC26A2))
| Chromosome |
5 |
| 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.149360517A>C |
| DNA change (hg38) |
g.149980954A>C |
| Published as |
a1388c: Q454P |
| ISCN |
- |
| DB-ID |
SLC26A2_000021 |
| Variant remarks |
1 Lebanese DTD family |
| Reference |
PubMed: Megarbane et al. 1999 |
| ClinVar ID |
- |
| dbSNP ID |
rs104893921 |
| 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 |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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