List of variants in gene TRIOBP reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.2477C>T (p.Ser826Leu)	rs41296243	0.01649
NM_001039141.3(TRIOBP):c.3089C>G (p.Pro1030Arg)	rs193043234	0.00922
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=)	rs375013523	0.00137
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser)	rs201794404	0.00115
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe)	rs199794705	0.00069
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=)	rs139074745	0.00058

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