Variant #0000815726 (NC_000007.13:g.107312690G>T, NM_000441.1:c.412G>T (SLC26A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107312690G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC26A4_000072 See all 13 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs111033199
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00017 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-10-21 18:26:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A4 NM_000441.1 +?/. - c.412G>T r.(?) p.(Val138Phe)


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