Variant #0000016774 (NC_000007.13:g.(?_107443556)_(107443678_?)del, NC_000007.13(NM_000111.2):c.-211-?_-89+?del (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.(?_107443556)_(107443678_?)del
DNA change (hg38) g.107803111_107803233del
Published as 8.6 kb deletion: Exon 1 deletion
ISCN -
DB-ID SLC26A3_000110
Variant remarks 1 Swedish 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 +?/+? _1_1i c.-211-?_-89+?del r.? p.?


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