Variant #0000016756 (NC_000007.13:g.107434303_107434315del, NM_000111.2:c.145_157del (SLC26A3))

Chromosome 7
Allele Both (homozygous)
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.107434303_107434315del
DNA change (hg38) g.107793858_107793870del
Published as c.145-157del13bp
ISCN -
DB-ID SLC26A3_000001 See all 3 reported entries
Variant remarks 2 Belgian siblings (Togo ancestry; hom) with DIAR1
Reference PubMed: Makela et al. 2002
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 13:23:57 +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 +?/+? 3 c.145_157del r.(145_157del) p.(Lys49Leufs*8)


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