List of variants reported as benign for Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins by Natera, Inc.

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_018006.5(TRMU):c.28G>T (p.Ala10Ser)	rs11090865	0.13476
NM_018006.5(TRMU):c.1176G>A (p.Thr392=)	rs34591580	0.06826
NM_018006.5(TRMU):c.1192C>T (p.Arg398Cys)	rs34152016	0.03308
NM_018006.5(TRMU):c.552C>T (p.Ala184=)	rs35772382	0.03164
NM_018006.5(TRMU):c.10T>G (p.Leu4Val)	rs114302881	0.02970
NM_018006.5(TRMU):c.927C>T (p.Arg309=)	rs9627420	0.02832
NM_018006.5(TRMU):c.9C>G (p.Ala3=)	rs75417986	0.02729
NM_018006.5(TRMU):c.*8G>C	rs55905826	0.01809
NM_018006.5(TRMU):c.442G>A (p.Glu148Lys)	rs34012206	0.01506
NM_018006.5(TRMU):c.479C>T (p.Ala160Val)	rs35338668	0.01380
NM_018006.5(TRMU):c.864C>T (p.Asp288=)	rs61737827	0.01333
NM_018006.5(TRMU):c.387A>G (p.Ala129=)	rs144586525	0.00478
NM_018006.5(TRMU):c.75G>T (p.Arg25Ser)	rs2272938	0.00065
NM_018006.5(TRMU):c.1158G>A (p.Leu386=)	rs79874854	0.00013
NM_018006.5(TRMU):c.272A>G (p.Lys91Arg)	rs138044544	0.00002
NM_018006.5(TRMU):c.567C>G (p.Ile189Met)	rs192537315

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