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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A2 NM_000112.3 +/+ 1i c.-26+2T>C r.[0,=] p.[0,=]


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