Variant #0000016782 (NC_000007.13:g.107432299C>T, NM_000111.2:c.358G>A (SLC26A3))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107432299C>T
DNA change (hg38) g.107791854C>T
Published as c.358G>A
ISCN -
DB-ID SLC26A3_000006 See all 2 reported entries
Variant remarks 1 Polish, 1 Swedish and 1 Norwegian DIAR1 family (all com-het)
Reference PubMed: Höglung et al. 1998, PubMed: Höglung et al. 2001b
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/100 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-10 17:16:02 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A3 NM_000111.2 +?/+? 4 c.358G>A r.(358g>a) p.(Gly120Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.