Variants in gene TRMU with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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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.1192C>T (p.Arg398Cys)	rs34152016	0.03308
NM_018006.5(TRMU):c.10T>G (p.Leu4Val)	rs114302881	0.02970
NM_018006.5(TRMU):c.387A>G (p.Ala129=)	rs144586525	0.00478
NM_018006.5(TRMU):c.900G>T (p.Leu300=)	rs113846383	0.00068
NM_018006.5(TRMU):c.772+8G>A	rs201372242	0.00048
NM_018006.5(TRMU):c.1158G>A (p.Leu386=)	rs79874854	0.00013
NM_018006.5(TRMU):c.910C>G (p.Leu304Val)	rs200777988	0.00011
NM_018006.5(TRMU):c.351T>C (p.Asn117=)	rs117710834	0.00009
NM_018006.5(TRMU):c.567C>G (p.Ile189Met)	rs192537315

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