List of variants in gene TRMU reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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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.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.83-19T>C	rs7290233	0.01253
NM_018006.5(TRMU):c.652-16C>T	rs73177076	0.00529
NM_018006.5(TRMU):c.387A>G (p.Ala129=)	rs144586525	0.00478
NM_018006.5(TRMU):c.238G>A (p.Asp80Asn)	rs55952751	0.00145
NM_018006.5(TRMU):c.900G>T (p.Leu300=)	rs113846383	0.00068
NM_018006.5(TRMU):c.75G>T (p.Arg25Ser)	rs2272938	0.00065
NM_018006.5(TRMU):c.772+8G>A	rs201372242	0.00048
NM_018006.5(TRMU):c.272A>G (p.Lys91Arg)	rs138044544	0.00002

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