List of variants in gene TRIO reported as uncertain significance by Invitae

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_007118.4(TRIO):c.5297C>G (p.Pro1766Arg)	rs1753762422	0.00001
NM_007118.4(TRIO):c.6568C>T (p.Leu2190Phe)	rs982795600	0.00001
NM_007118.4(TRIO):c.2668C>A (p.Gln890Lys)
NM_007118.4(TRIO):c.3212T>G (p.Leu1071Arg)	rs2152344481
NM_007118.4(TRIO):c.382G>A (p.Val128Met)
NM_007118.4(TRIO):c.3949-6G>A
NM_007118.4(TRIO):c.4127G>C (p.Trp1376Ser)	rs79341256
NM_007118.4(TRIO):c.4267A>T (p.Ile1423Phe)	rs1747350463
NM_007118.4(TRIO):c.4778G>A (p.Arg1593Gln)	rs1404663085
NM_007118.4(TRIO):c.59C>T (p.Ala20Val)
NM_007118.4(TRIO):c.6072C>G (p.Asp2024Glu)	rs1754871642
NM_007118.4(TRIO):c.6221A>G (p.Glu2074Gly)
NM_007118.4(TRIO):c.6810A>T (p.Leu2270Phe)
NM_007118.4(TRIO):c.7309G>T (p.Ala2437Ser)
NM_007118.4(TRIO):c.7432C>T (p.Pro2478Ser)
NM_007118.4(TRIO):c.7543C>T (p.Arg2515Cys)	rs766894115
NM_007118.4(TRIO):c.7741C>A (p.Leu2581Met)

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