List of variants in gene TRAPPC4 reported as uncertain significance for Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

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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_016146.6(TRAPPC4):c.176-3C>T	rs1193834176	0.00001
NM_016146.6(TRAPPC4):c.278C>T (p.Pro93Leu)	rs1307746359	0.00001
NM_016146.6(TRAPPC4):c.191T>C (p.Leu64Pro)	rs1943259006
NM_016146.6(TRAPPC4):c.260G>A (p.Gly87Asp)
NM_016146.6(TRAPPC4):c.64T>C (p.Tyr22His)

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