List of variants in gene TRRAP reported as uncertain significance for See cases

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001375524.1(TRRAP):c.634-3C>T	rs113339948	0.00024
NM_001375524.1(TRRAP):c.10390G>T (p.Ala3464Ser)
NM_001375524.1(TRRAP):c.2465C>T (p.Pro822Leu)	rs2116445926
NM_001375524.1(TRRAP):c.4087G>A (p.Val1363Ile)
NM_001375524.1(TRRAP):c.4953+5C>T
NM_001375524.1(TRRAP):c.7176+4A>G	rs2116686587
NM_001375524.1(TRRAP):c.8090C>G (p.Pro2697Arg)	rs753661271
NM_001375524.1(TRRAP):c.9356C>G (p.Ala3119Gly)	rs2116768843

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