ClinVar Miner

List of variants in gene RDX studied for autosomal recessive nonsyndromic deafness 24

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
Download table as spreadsheet
HGVS dbSNP
NM_001260493.1(RDX):c.-240C>G
NM_001260493.1(RDX):c.-270G>C
NM_001260493.1(RDX):c.-272A>T
NM_001260493.1(RDX):c.-285A>G
NM_001260493.1(RDX):c.-291G>A
NM_001260494.1(RDX):c.60-5775C>T rs121918380
NM_001260496.1(RDX):c.405-1415dup
NM_002906.3(RDX):c.*1058G>A rs886047643
NM_002906.3(RDX):c.*1083G>A rs114509945
NM_002906.3(RDX):c.*1173A>G rs753716470
NM_002906.3(RDX):c.*1251A>C rs541339386
NM_002906.3(RDX):c.*1284G>A rs74676538
NM_002906.3(RDX):c.*1290A>G rs867786685
NM_002906.3(RDX):c.*1313G>C rs189484152
NM_002906.3(RDX):c.*1368A>C rs540576204
NM_002906.3(RDX):c.*156A>G rs186249296
NM_002906.3(RDX):c.*1579A>G rs772084374
NM_002906.3(RDX):c.*1955A>G rs138942667
NM_002906.3(RDX):c.*1961G>A rs746061486
NM_002906.3(RDX):c.*2006A>G rs538806036
NM_002906.3(RDX):c.*2057T>C rs886047633
NM_002906.3(RDX):c.*2423C>T rs886047632
NM_002906.3(RDX):c.*429G>A rs146390813
NM_002906.3(RDX):c.*463A>G rs886047645
NM_002906.3(RDX):c.*79A>C rs55953813
NM_002906.3(RDX):c.*800C>T rs886047644
NM_002906.3(RDX):c.*885G>A rs142279957
NM_002906.3(RDX):c.-105C>T rs78818014
NM_002906.3(RDX):c.-149C>T rs575111883
NM_002906.3(RDX):c.-169C>T rs371468276
NM_002906.3(RDX):c.-179C>T rs886047653
NM_002906.3(RDX):c.-221C>A rs886047654
NM_002906.3(RDX):c.-290C>A rs886047655
NM_002906.3(RDX):c.-297C>T rs886047656
NM_002906.3(RDX):c.-305G>T rs886047657
NM_002906.3(RDX):c.-309T>G rs886047658
NM_002906.3(RDX):c.-65+12C>T rs886047651
NM_002906.3(RDX):c.-76C>T rs886047652
NM_002906.3(RDX):c.1049G>A (p.Arg350His) rs377016439
NM_002906.3(RDX):c.1059A>G (p.Gln353=) rs139953187
NM_002906.3(RDX):c.1162C>A (p.Arg388=) rs754563690
NM_002906.3(RDX):c.1188T>C (p.Ala396=) rs886047647
NM_002906.3(RDX):c.1195G>A (p.Ala399Thr) rs886047646
NM_002906.3(RDX):c.1345-7T>C rs142161673
NM_002906.3(RDX):c.1411C>G (p.Pro471Ala) rs138560358
NM_002906.3(RDX):c.1487C>T (p.Ala496Val) rs74983220
NM_002906.3(RDX):c.1504A>G (p.Asn502Asp) rs140180881
NM_002906.3(RDX):c.1530C>T (p.Ser510=) rs192239366
NM_002906.3(RDX):c.1732G>A (p.Asp578Asn) rs121918379
NM_002906.3(RDX):c.354G>T (p.Pro118=) rs144543614
NM_002906.3(RDX):c.507A>G (p.Glu169=) rs886047648
NM_002906.3(RDX):c.551+2T>C
NM_002906.3(RDX):c.573C>A (p.Tyr191Ter) rs139960434
NM_002906.3(RDX):c.602A>G (p.Tyr201Cys) rs146019940
NM_002906.3(RDX):c.698+1G>A
NM_002906.3(RDX):c.836G>T (p.Arg279Leu) rs150863373
NM_002906.3(RDX):c.910C>T (p.Gln304Ter) rs893826250
NM_002906.4(RDX):c.*1143G>A
NM_002906.4(RDX):c.*1201A>G
NM_002906.4(RDX):c.*1215G>A
NM_002906.4(RDX):c.*1264G>C
NM_002906.4(RDX):c.*1358C>T
NM_002906.4(RDX):c.*1375G>A
NM_002906.4(RDX):c.*1383G>A
NM_002906.4(RDX):c.*1536T>C
NM_002906.4(RDX):c.*1632A>G
NM_002906.4(RDX):c.*1898A>G
NM_002906.4(RDX):c.*2070A>G
NM_002906.4(RDX):c.*2085A>C
NM_002906.4(RDX):c.*2112A>G
NM_002906.4(RDX):c.*2253C>T
NM_002906.4(RDX):c.*302C>T
NM_002906.4(RDX):c.*414A>T
NM_002906.4(RDX):c.*474A>G
NM_002906.4(RDX):c.*740C>T
NM_002906.4(RDX):c.*762C>A
NM_002906.4(RDX):c.*855T>C
NM_002906.4(RDX):c.-133C>T
NM_002906.4(RDX):c.-91G>A
NM_002906.4(RDX):c.1251+14T>G
NM_002906.4(RDX):c.1495G>C (p.Glu499Gln)
NM_002906.4(RDX):c.1547C>T (p.Thr516Ile)
NM_002906.4(RDX):c.1577A>G (p.Lys526Arg)
NM_002906.4(RDX):c.301C>T (p.Leu101Phe)
NM_002906.4(RDX):c.698+14T>C
NM_002906.4(RDX):c.6G>A (p.Pro2=)

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.