All variants in the SLC26A4 gene

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)     

Published as     

RNA change     

Protein     

Clinical classification     

DNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Owner     
+/. - c.1343C>T - r.(?) p.(Ser448Leu) Likely pathogenic g.107694622C>T - Yock-Ping Chow et al.(2017) SLC26A4_000001 rs747076316 - - Nur Aisyah Athirah
+/. - c.1343C>T - r.(?) p.(Ser448Leu) Likely pathogenic g.107694622C>T - Yock-Ping Chow et al.(2017) SLC26A4_000001 rs747076316 - - Nur Aisyah Athirah
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