Variant #0000016781 (NC_000007.13:g.107432313del, NM_000111.2:c.344del (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.107432313del
DNA change (hg38) g.107791868del
Published as c.344delT
ISCN -
DB-ID SLC26A3_000117
Variant remarks 2 Polish DIAR1 families ( 1 hom and 1 het)
Reference PubMed: Höglung et al. 1996
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/159 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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 13:23:52 +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 +?/+? 4 c.344del r.(?) p.(Ile115Thrfs*19)


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