Variant #0000018267 (NC_000007.13:g.107423719T>G, NC_000007.13(NM_000111.2):c.1047+3A>C (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.107423719T>G
DNA change (hg38) g.107783274T>G
Published as -
ISCN -
DB-ID SLC26A3_000135
Variant remarks 1 Korean DIAR1 patient (com-het)
Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference PubMed: Hong et al. 2013
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 2013-06-19 22:49:27 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A3 NM_000111.2 +?/+? 9 c.1047+3A>C r.spl? p.?


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