ClinVar Miner

List of variants in gene combination ANAPC15, LRTOMT reported as uncertain significance for auditory system disorder

Included ClinVar conditions (322):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
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

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