ClinVar Miner

List of variants in gene SLC26A4 studied for Nonsyndromic Hearing Loss, Recessive

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
Download table as spreadsheet
HGVS dbSNP
NM_000441.1(SLC26A4):c.-139C>T rs879914861
NM_000441.1(SLC26A4):c.-186A>G rs555307083
NM_000441.1(SLC26A4):c.-66C>G rs17154282
NM_000441.2(SLC26A4):c.*1059T>C rs183926745
NM_000441.2(SLC26A4):c.*1123A>G rs141341508
NM_000441.2(SLC26A4):c.*1200G>A rs549659217
NM_000441.2(SLC26A4):c.*1277A>G rs560359006
NM_000441.2(SLC26A4):c.*1517G>C rs2712205
NM_000441.2(SLC26A4):c.*1584dup rs886061890
NM_000441.2(SLC26A4):c.*1610C>T rs192222034
NM_000441.2(SLC26A4):c.*1640G>T rs886061891
NM_000441.2(SLC26A4):c.*1797G>C rs76820337
NM_000441.2(SLC26A4):c.*1875G>C rs886061892
NM_000441.2(SLC26A4):c.*1960T>A rs886061893
NM_000441.2(SLC26A4):c.*2047A>G rs534409544
NM_000441.2(SLC26A4):c.*2147G>A rs886061894
NM_000441.2(SLC26A4):c.*2250_*2251del rs886061895
NM_000441.2(SLC26A4):c.*239C>T rs113516368
NM_000441.2(SLC26A4):c.*343C>A rs139104953
NM_000441.2(SLC26A4):c.*409A>T rs752578836
NM_000441.2(SLC26A4):c.*523A>G rs560536749
NM_000441.2(SLC26A4):c.*614C>T rs77315223
NM_000441.2(SLC26A4):c.*618A>G rs886061888
NM_000441.2(SLC26A4):c.*69C>A rs76894072
NM_000441.2(SLC26A4):c.*780T>C rs527503006
NM_000441.2(SLC26A4):c.*791A>G rs146458433
NM_000441.2(SLC26A4):c.*840C>T rs886061889
NM_000441.2(SLC26A4):c.*868G>A rs2712218
NM_000441.2(SLC26A4):c.-8G>A rs886061882
NM_000441.2(SLC26A4):c.1050G>A (p.Leu350=) rs727504993
NM_000441.2(SLC26A4):c.1068C>T (p.Ile356=) rs886061885
NM_000441.2(SLC26A4):c.1069G>A (p.Ala357Thr) rs145467740
NM_000441.2(SLC26A4):c.1110A>G (p.Val370=) rs886061886
NM_000441.2(SLC26A4):c.1826T>G (p.Val609Gly) rs17154335
NM_000441.2(SLC26A4):c.2008G>A (p.Val670Ile) rs201689637
NM_000441.2(SLC26A4):c.2018T>G (p.Val673Gly) rs886061887
NM_000441.2(SLC26A4):c.2135A>G (p.Asn712Ser) rs772522003
NM_000441.2(SLC26A4):c.2291C>T (p.Thr764Met) rs150597240
NM_000441.2(SLC26A4):c.2320-4A>G rs727503432
NM_000441.2(SLC26A4):c.371T>A (p.Ile124Asn) rs886061883
NM_000441.2(SLC26A4):c.601-5C>T rs546450643
NM_000441.2(SLC26A4):c.841G>A (p.Val281Ile) rs727505080
NM_000441.2(SLC26A4):c.872G>A (p.Arg291Gln) rs138816005
NM_000441.2(SLC26A4):c.887T>A (p.Ile296Asn) rs886061884
NM_000441.2(SLC26A4):c.888C>T (p.Ile296=) rs765095794

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.