Variant #0000016476 (NC_000005.9:g.149357747C>T, NM_000112.3:c.532C>T (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.149357747C>T
DNA change (hg38) g.149978184C>T
Published as c559t: R178X
ISCN -
DB-ID SLC26A2_000011 See all 4 reported entries
Variant remarks Several DTD patients of various ethnicity; Functional studies show dicreased sulfate transport activity
Reference PubMed: Superti-Furga et al. 1996b, PubMed: Superti-Furga et al. 1996a, PubMed: Barbosa et al. 2011
ClinVar ID -
dbSNP ID rs104893919
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
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 18:33:04 +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 +/+ 2 c.532C>T r.(532c>u) p.(Arg178*)


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