Variant #0000016744 (NC_000007.13:g.107423510_107423511del, NM_000111.2:c.1148_1149del (SLC26A3))

Chromosome 7
Allele Paternal (confirmed)
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.107423510_107423511del
DNA change (hg38) g.107783065_107783066del
Published as deletion at 1148–1149 of a TA dinucleotide: frameshift, truncated protein product 455 amino acids long
ISCN -
DB-ID SLC26A3_000080
Variant remarks 2 Andalusian (southern Spain) sibs (com-het) and 1 Spanish DIAR1 patient
Reference PubMed: Rodriques-Herrera et al. 2011, PubMed: Wedenoja et al. 2011
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 2012-12-10 17:16:02 +01:00 (CET)
Date last edited 2020-06-23 13:23:32 +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 +/+ 10 c.1148_1149del r.(?) p.(Ile383Serfs*74)


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