List of variants in gene TRIM54 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_187841.3(TRIM54):c.584T>G (p.Met195Arg)	rs139128442	0.00060
NM_187841.3(TRIM54):c.394G>T (p.Glu132Ter)	rs146448995	0.00039
NM_187841.3(TRIM54):c.513+1del	rs750473735
NM_187841.3(TRIM54):c.610-6T>G
NM_187841.3(TRIM54):c.992-1G>A	rs1337492672

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