Variant #0000016796 (NC_000007.13:g.(?_107427272)_(107427954_?)del, NC_000007.13(NM_000111.2):c.736-?_971+?del (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.(?_107427272)_(107427954_?)del
DNA change (hg38) g.107786827_107787509del
Published as 3.5 kb genomic deletion: EX7-8del
ISCN -
DB-ID SLC26A3_000132
Variant remarks 2 Japanese siblings (hom) with DIAR1
Reference PubMed: Höglung et al. 2001b
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 2012-12-10 17:16:02 +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     
SLC26A3 NM_000111.2 +?/+? 6i_8i c.736-?_971+?del r.(736_971del) p.(Val246Ilefs*8)


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