Full data view for gene SLC26A4


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000441.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

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Panel size     

Owner     
+/. - c.241A>G r,(?) p.(Lys81Glu) Parent #1 - pathogenic (recessive) g.107303817A>G g.107663372A>G - - SLC26A4_000287 combination of alleles not reported PubMed: Wu 2019 - - Germline - 1/1291 cases hearing loss - - - DNA SEQ, SEQ-NG - 213-gene panel HL - PubMed: Wu 2019 analysis 1291 cases hearing loss - - Taiwan - - - - - 1 Johan den Dunnen
+?/. - c.241A>G r.(?) p.(Lys81Glu) Parent #1 ACMG likely pathogenic (recessive) g.107303817A>G g.107663372A>G - - SLC26A4_000287 ACMG PM2, PM3, PP3, PP4 PubMed: Lin 2019 - - Germline - - - - - DNA SEQ-NG - SLC26A4, FOXI1, KCNJ10 HL DE1021 PubMed: Lin 2019 - - - Taiwan - - - - - 1 Johan den Dunnen
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