Variant #0000016489 (NC_000005.9:g.149360630C>T, NM_000112.3:c.1474C>T (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.149360630C>T |
DNA change (hg38) |
g.149981067C>T |
Published as |
1501C>T: R492W |
ISCN |
- |
DB-ID |
SLC26A2_000003 See all 8 reported entries |
Variant remarks |
DTD mutation, seen in several DTD patients |
Reference |
PubMed: Rossi et al. 2001 |
ClinVar ID |
- |
dbSNP ID |
rs78676079 |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.01674 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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