List of variants in gene TRMU reported as likely 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: 24

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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.900G>T (p.Leu300=)	rs113846383	0.00068
NM_018006.5(TRMU):c.-44G>A	rs370964036	0.00021
NM_018006.5(TRMU):c.-36C>G	rs560661382	0.00013
NM_018006.5(TRMU):c.1158G>A (p.Leu386=)	rs79874854	0.00013
NM_018006.5(TRMU):c.430G>A (p.Val144Ile)	rs367570778	0.00010
NM_018006.5(TRMU):c.479-10T>C	rs202070165	0.00009
NM_018006.5(TRMU):c.-19G>C	rs886057609	0.00008
NM_018006.5(TRMU):c.1164G>A (p.Pro388=)	rs202047181	0.00004
NM_018006.5(TRMU):c.1193G>A (p.Arg398His)	rs139351059	0.00004
NM_018006.5(TRMU):c.429C>T (p.His143=)	rs746421213	0.00004
NM_018006.5(TRMU):c.873+12G>A	rs540183174	0.00004
NM_018006.5(TRMU):c.-15T>C	rs764076380	0.00003
NM_018006.5(TRMU):c.1246G>T (p.Gly416Cys)	rs150043707	0.00003
NM_018006.5(TRMU):c.469G>A (p.Val157Ile)	rs201755743	0.00003
NM_018006.5(TRMU):c.83-11C>A	rs1057523042	0.00003
NM_018006.5(TRMU):c.576G>C (p.Leu192=)	rs1319509730	0.00001
NM_018006.5(TRMU):c.772+11G>C	rs1262602634	0.00001
NM_018006.5(TRMU):c.942G>A (p.Ala314=)	rs767891094	0.00001
NM_018006.5(TRMU):c.1093A>C (p.Thr365Pro)	rs138586787
NM_018006.5(TRMU):c.1125C>A (p.Asp375Glu)	rs779022860
NM_018006.5(TRMU):c.248+19A>C	rs1057521579
NM_018006.5(TRMU):c.567C>G (p.Ile189Met)	rs192537315
NM_018006.5(TRMU):c.768T>C (p.His256=)	rs1555899299

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