Variant #0000016474 (NC_000005.9:g.149357618C>A, NM_000112.3:c.403C>A (SLC26A2))

Chromosome 5
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.149357618C>A
DNA change (hg38) g.149978055C>A
Published as 430C>A: Q135R
ISCN -
DB-ID SLC26A2_000009
Variant remarks Rare French DTD mutation
Reference PubMed: Rossi et al. 2001
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 2012-11-15 14:17:13 +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     
SLC26A2 NM_000112.3 +?/+? 2 c.403C>A r.(403c>a) p.(Gln135Lys)


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