ClinVar Miner

List of variants in gene ANAPC15, LRTOMT studied for autosomal recessive nonsyndromic hearing loss 63

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014042.3(ANAPC15):c.*79A>G rs113912971 0.01193
NM_014042.3(ANAPC15):c.121-132T>A rs142914900 0.00418
NM_014042.3(ANAPC15):c.181-63G>T rs759367241 0.00031
NM_014042.3(ANAPC15):c.*105C>T rs186960319 0.00021
NM_014042.3(ANAPC15):c.296C>T (p.Pro99Leu) rs531848254 0.00016
NM_014042.3(ANAPC15):c.180+75T>C rs912805774 0.00014
NM_014042.3(ANAPC15):c.318+3A>G rs201099496 0.00010
NM_014042.3(ANAPC15):c.318+47C>T rs375298971 0.00004
NM_014042.3(ANAPC15):c.180+11C>G rs769123440 0.00001
NM_014042.3(ANAPC15):c.256A>T (p.Met86Leu) rs1469899576 0.00001
NM_014042.3(ANAPC15):c.*96C>T rs1946187692
NM_014042.3(ANAPC15):c.121-110G>C rs886048640
NM_014042.3(ANAPC15):c.121-95G>A rs561162900
NM_014042.3(ANAPC15):c.180+131A>C rs932792064

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.