Variant #0000016747 (NC_000007.13:g.107434821_107434822ins288, NC_000007.13(NM_000111.2):c.131+2_131+3ins288 (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.107434821_107434822ins288
DNA change (hg38) -
Published as c.131+2_131+3insU14569.1
ISCN -
DB-ID SLC26A3_000083
Variant remarks 1 Qatar DIAR1 patient; 288 bp sequence U14569.1 (genebank no) is inserted between bases c.131+2 and c.131+3
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 +?/+? 2i c.131+2_131+3ins288 r.? p.?


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