Variant #0000016494 (NC_000005.9:g.149361113T>A, NM_000112.3:c.1957T>A (SLC26A2))
Chromosome |
5 |
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.149361113T>A |
DNA change (hg38) |
g.149981550T>A |
Published as |
1984T>A: C653S |
ISCN |
- |
DB-ID |
SLC26A2_000028 See all 3 reported entries |
Variant remarks |
DTD mutation, observed in several DTD patients and also in one rMED DTD patient. |
Reference |
PubMed: Rossi et al. 2001 |
ClinVar ID |
- |
dbSNP ID |
rs104893924 |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
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 18:33:04 +02:00 (CEST) |

Variant on transcripts
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