Variant #0000016497 (NC_000005.9:g.149361150A>C, NM_000112.3:c.1994A>C (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.149361150A>C
DNA change (hg38) g.149981587A>C
Published as 2021A>C: H665P
ISCN -
DB-ID SLC26A2_000031 See all 4 reported entries
Variant remarks Rare Canadian-British DTD mutation
Reference PubMed: Rossi et al. 2001
ClinVar ID -
dbSNP ID rs141798540
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-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 2012-11-15 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 +?/+? 3 c.1994A>C r.(1994a>c) p.(His665Pro)


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