Variant #0000016486 (NC_000005.9:g.149360517A>C, NM_000112.3:c.1361A>C (SLC26A2))

Chromosome 5
Allele Both (homozygous)
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.149360517A>C
DNA change (hg38) g.149980954A>C
Published as a1388c: Q454P
ISCN -
DB-ID SLC26A2_000021
Variant remarks 1 Lebanese DTD family
Reference PubMed: Megarbane et al. 1999
ClinVar ID -
dbSNP ID rs104893921
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 19:04:32 +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.1361A>C r.(1361a>c) p.(Gln454Pro)


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