Variant #0000016491 (NC_000005.9:g.149360806del, NM_000112.3:c.1650del (SLC26A2))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.149360806del |
DNA change (hg38) |
g.149981243del |
Published as |
1677delG: FS/stop |
ISCN |
- |
DB-ID |
SLC26A2_000025 |
Variant remarks |
Rare British-Italian DTD mutation |
Reference |
PubMed: Rossi et al. 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-11-15 14:17:13 +01:00 (CET) |
Date last edited |
2020-06-18 08:52:18 +02:00 (CEST) |

Variant on transcripts
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