Genomic variant #0000016481

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.149360062_149360063del
DNA change (hg38) g.149980499_149980500del
Published as 933-934delCT: FS/stop
ISCN -
DB-ID SLC26A2_000016
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 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Anne Polvi
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A2 NM_000112.3 +/+ 3 c.906_907del r.(?) p.(Cys303*)