Database of Pathogenic Variants
Home
Variants
Diseases
Genes
About
Gene Detail
Gene Symbol
SLC26A4
Gene:5172
HGNC:8818
Gene Name
solute carrier family 26 member 4
Chromosome
7
Cytogenetic Band
q22.3
RefSeq Accession
NM_000441
Associated Diseases
Deafness, autosomal recessive, 4
Associated Variants
NM_000441.1:c.367C>T
NM_000441.1:c.416-1G>A
NM_000441.1:c.439A>G
NM_000441.1:c.600+1G>T
NM_000441.1:c.601-1G>A
NM_000441.1:c.890C>A
NM_000441.1:c.919-2A>G
NM_000441.1:c.1001+1G>A
NM_000441.1:c.1105A>G
NM_000441.1:c.1115C>T
NM_000441.1:c.1174A>T
NM_000441.1:c.1187G>A
NM_000441.1:c.1229C>T
NM_000441.1:c.1315G>A
NM_000441.1:c.1586T>G
NM_000441.1:c.1743G>C
NM_000441.1:c.1970G>A
NM_000441.1:c.1997C>T
NM_000441.1:c.2162C>T
NM_000441.1:c.2167C>T
NM_000441.1:c.2168A>G
NM_000441.1:c.82A>G
NM_000441.1:c.1226G>A
NM_000441.1:c.1614+1G>A
NM_000441.1:c.1651dupT
NM_000441.1:c.1667A>G
NM_000441.1:c.1707+5G>A
NM_000441.1:c.1708-27_1708-11del17
NM_000441.1:c.2074T>C
NM_000441.1:c.2228T>A
NM_000441.1:c.322delC
NM_000441.1:c.1079C>T
NM_000441.1:c.1625C>G
NM_000441.1:c.1829C>A
NM_000441.1:c.916dupG
NM_000441.1:c.2106_2110dupGCTGG