Variant #0000016798 (NC_000007.13:g.107427292_107427294del, NM_000111.2:c.951_953del (SLC26A3))

Chromosome 7
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.107427292_107427294del
DNA change (hg38) g.107786847_107786849del
Published as c.951delGGT
ISCN -
DB-ID SLC26A3_000134
Variant remarks Finnish major DIAR1 mutation. 45 Finnish (and Swedish) DIAR1 patients
Reference PubMed: Höglung et al. 1996, PubMed: Wedenoja et al. 2011
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 3/436 FIN (het)
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 13:23:38 +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 +/+ 8 c.951_953del r.(?) p.(Val318del)


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