Variant #0000016786 (NC_000007.13:g.107431671G>A, NM_000111.2:c.392C>T (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.107431671G>A
DNA change (hg38) g.107791226G>A
Published as c.392C>T
ISCN -
DB-ID SLC26A3_000011 See all 2 reported entries
Variant remarks 1 American DIAR1 patient and 2 Korean siblings with DIAR1
Reference PubMed: Wedenoja et al. 2011, PubMed: Hong et al. 2013
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 18:33:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A3 NM_000111.2 +?/+? 5 c.392C>T r.(392c>u) p.(Pro131Leu)


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