ClinVar Miner

List of variants in gene GRXCR1 studied for Autosomal recessive nonsyndromic hearing loss 25

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001080476.3(GRXCR1):c.*55G>A rs4861050 0.45974
NM_001080476.3(GRXCR1):c.140C>T (p.Ala47Val) rs57655409 0.07551
NM_001080476.3(GRXCR1):c.777C>T (p.Ser259=) rs61733348 0.01525
NM_001080476.3(GRXCR1):c.272G>T (p.Gly91Val) rs113203706 0.00339
NM_001080476.3(GRXCR1):c.785G>A (p.Arg262Gln) rs146696590 0.00067
NM_001080476.3(GRXCR1):c.*65A>G rs531527331 0.00045
NM_001080476.3(GRXCR1):c.*89G>A rs564643132 0.00034
NM_001080476.3(GRXCR1):c.627+19A>T rs201824235 0.00021
NM_001080476.3(GRXCR1):c.331T>C (p.Tyr111His) rs201002003 0.00016
NM_001080476.3(GRXCR1):c.439C>T (p.Arg147Cys) rs569193097 0.00009
NM_001080476.3(GRXCR1):c.284G>C (p.Arg95Thr) rs775363257 0.00004
NM_001080476.3(GRXCR1):c.325G>A (p.Val109Ile) rs760182093 0.00004
NM_001080476.3(GRXCR1):c.49C>T (p.Arg17Trp) rs762049276 0.00004
NM_001080476.3(GRXCR1):c.*69T>A rs796495255 0.00003
NM_001080476.3(GRXCR1):c.236G>A (p.Ser79Asn) rs886059416 0.00003
NM_001080476.3(GRXCR1):c.289G>A (p.Val97Ile) rs186041671 0.00003
NM_001080476.3(GRXCR1):c.551A>T (p.Glu184Val) rs886059417 0.00003
NM_001080476.3(GRXCR1):c.628-9C>A rs606231120 0.00003
NM_001080476.3(GRXCR1):c.*6G>T rs1344018880 0.00001
NM_001080476.3(GRXCR1):c.358T>C (p.Phe120Leu) rs529420082 0.00001
NM_001080476.3(GRXCR1):c.412C>T (p.Arg138Cys) rs267606856 0.00001
NM_001080476.3(GRXCR1):c.469G>T (p.Glu157Ter) rs774844858 0.00001
NM_001080476.3(GRXCR1):c.79C>T (p.Arg27Ter) rs769983282 0.00001
NM_001080476.3(GRXCR1):c.229C>T (p.Gln77Ter) rs267606855
NM_001080476.3(GRXCR1):c.25G>A (p.Glu9Lys) rs78136490
NM_001080476.3(GRXCR1):c.385-2A>G rs771844359
NM_001080476.3(GRXCR1):c.385-7C>T rs748066741
NM_001080476.3(GRXCR1):c.457T>G (p.Phe153Val)
NM_001080476.3(GRXCR1):c.550G>T (p.Glu184Ter) rs2109775078
NM_001080476.3(GRXCR1):c.604T>C (p.Phe202Leu) rs886059418
NM_001080476.3(GRXCR1):c.627+8A>C rs10213360
NM_001080476.3(GRXCR1):c.668T>A (p.Leu223Gln)
NM_001080476.3(GRXCR1):c.745C>G (p.Pro249Ala) rs886059419
NM_001080476.3(GRXCR1):c.858G>T (p.Lys286Asn) rs886059420

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.