Variant #0000016468 (NC_000005.9:g.149340544T>C, NC_000005.9(NM_000112.3):c.-26+2T>C (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.149340544T>C |
DNA change (hg38) |
g.149960981T>C |
Published as |
c.-26+2T>C: DTDSTFin; IVS1+2T>C |
ISCN |
- |
DB-ID |
SLC26A2_000004 See all 2 reported entries |
Variant remarks |
Finnish DTD Founder/Major mutation: ~80% of Finnish DTD patients (most hom). Also in ~18% of non-Finnish DTD patients. |
Reference |
PubMed: Hästbacka et al. 1999, PubMed: Dwyer et al. 2010, PubMed: Mäkitie et al. 2014 |
ClinVar ID |
- |
dbSNP ID |
- |
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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