Variant #0000016479 (NC_000005.9:g.149359920G>A, NM_000112.3:c.764G>A (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.149359920G>A
DNA change (hg38) g.149980357G>A
Published as g791a (G255E)
ISCN -
DB-ID SLC26A2_000014
Variant remarks Several DTD patients of various ethnicity; Functional studies show dicreased sulfate transport activity
Reference PubMed: Hästbacka et al. 1994, PubMed: Superti-Furga et al. 1996b, PubMed: Superti-Furga et al. 1996a
ClinVar ID -
dbSNP ID rs104893917
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 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 +/+ 3 c.764G>A r.(764g>a) p.(Gly255Glu)


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