ClinVar Miner

List of variants in gene DIAPH1 reported as pathogenic for autosomal dominant nonsyndromic hearing loss 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005219.5(DIAPH1):c.1549C>T (p.Gln517Ter) rs2099895754 0.00001
NM_005219.5(DIAPH1):c.3022C>T (p.Arg1008Ter) rs1461242879 0.00001
NC_000005.10:g.(?_141516831)_(141618934_?)del
NM_005219.5(DIAPH1):c.1016del (p.Met339fs) rs2154596448
NM_005219.5(DIAPH1):c.1051C>T (p.Arg351Ter)
NM_005219.5(DIAPH1):c.108dup (p.Lys37Ter) rs2154597562
NM_005219.5(DIAPH1):c.1483C>T (p.Arg495Ter)
NM_005219.5(DIAPH1):c.2100dup (p.Pro701fs) rs2154596284
NM_005219.5(DIAPH1):c.2108dup (p.Pro704fs) rs771360300
NM_005219.5(DIAPH1):c.2350_2351dup (p.Trp784fs)
NM_005219.5(DIAPH1):c.2540_2541del (p.Lys847fs) rs2099888710
NM_005219.5(DIAPH1):c.3166C>T (p.Gln1056Ter) rs1331356644
NM_005219.5(DIAPH1):c.3211_3212insAT (p.Arg1071fs)
NM_005219.5(DIAPH1):c.3268dup (p.Met1090fs) rs1235751512
NM_005219.5(DIAPH1):c.3624_3625del (p.Ala1210fs) rs1064797096
NM_005219.5(DIAPH1):c.3637C>T (p.Arg1213Ter) rs876657776
NM_005219.5(DIAPH1):c.3661+1G>T rs1476157529
NM_005219.5(DIAPH1):c.626dup (p.Tyr209Ter)
NM_005219.5(DIAPH1):c.684+1G>A
NM_005219.5(DIAPH1):c.839del (p.Leu280fs)
NM_005219.5(DIAPH1):c.89del (p.Gly30fs)
NM_005219.5(DIAPH1):c.910dup (p.Ser304fs) rs2154596461

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.