ClinVar Miner

List of variants in gene TMEM132E studied for auditory system disorder

Included ClinVar conditions (325):
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Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001304438.2(TMEM132E):c.-32T>C rs4795938 0.89192
NM_001304438.2(TMEM132E):c.67+48T>C rs7218304 0.66325
NM_001304438.2(TMEM132E):c.257A>C (p.Glu86Ala) rs147874855 0.00040
NM_001304438.2(TMEM132E):c.1529G>A (p.Arg510Gln) rs139895222 0.00003
NM_001304438.2(TMEM132E):c.2730C>G (p.Ile910Met) rs763524517 0.00002
NM_001304438.2(TMEM132E):c.2474C>T (p.Pro825Leu) rs370232097 0.00001
NM_001304438.2(TMEM132E):c.382G>T (p.Ala128Ser) rs766225189 0.00001
NM_001304438.2(TMEM132E):c.809G>A (p.Arg270His) rs570477617 0.00001
NM_001304438.2(TMEM132E):c.1228A>G (p.Met410Val) rs1907257569
NM_001304438.2(TMEM132E):c.1705G>A (p.Glu569Lys)

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