Variant #0000016742 (NC_000007.13:g.107423722_107423739delinsGGCATC, NM_000111.2:c.1030_1047delinsGATGCC (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.107423722_107423739delinsGGCATC
DNA change (hg38) g.107783277_107783294delinsGGCATC
Published as c.1030_1047delinsGATGCC
ISCN -
DB-ID SLC26A3_000022 See all 2 reported entries
Variant remarks 1 Polish DIAR1 patient
Reference 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 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 +?/+? 9 c.1030_1047delinsGATGCC r.(1030_1047delinsgaugcc) p.(Phe344_Val349delinsAspAla)


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