List of variants reported as likely pathogenic for Aminoglycoside-induced deafness; Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_018006.5(TRMU):c.249-2A>G	rs768299416	0.00002
NM_018006.5(TRMU):c.1019-1G>A	rs773484808
NM_018006.5(TRMU):c.333dup (p.His112fs)	rs756600903
NM_018006.5(TRMU):c.356-2_356-1del	rs2147053913
NM_018006.5(TRMU):c.87C>G (p.Tyr29Ter)	rs769668643

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