List of variants in gene TRAIP reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005879.3(TRAIP):c.303G>A (p.Gln101=)	rs145932323	0.00538
NM_005879.3(TRAIP):c.603T>C (p.Cys201=)	rs531391341	0.00006
NM_005879.3(TRAIP):c.1004G>T (p.Gly335Val)	rs144992965
NM_005879.3(TRAIP):c.470G>A (p.Arg157His)
NM_005879.3(TRAIP):c.624C>T (p.Tyr208=)
NM_005879.3(TRAIP):c.864C>T (p.Val288=)
NM_005879.3(TRAIP):c.898G>A (p.Glu300Lys)

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