List of variants in gene TRIO reported as pathogenic by SIB Swiss Institute of Bioinformatics

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_007118.4(TRIO):c.3232C>G (p.Arg1078Gly)	rs1554065887
NM_007118.4(TRIO):c.3232C>T (p.Arg1078Trp)
NM_007118.4(TRIO):c.3233G>A (p.Arg1078Gln)	rs1745369142
NM_007118.4(TRIO):c.3239A>T (p.Asn1080Ile)	rs879255628
NM_007118.4(TRIO):c.3895G>A (p.Glu1299Lys)	rs1746763024
NM_007118.4(TRIO):c.4283G>A (p.Arg1428Gln)	rs879255626
NM_007118.4(TRIO):c.4381C>A (p.Pro1461Thr)	rs879255627
NM_007118.4(TRIO):c.4382C>T (p.Pro1461Leu)	rs1747667518
NM_007118.4(TRIO):c.4406A>G (p.His1469Arg)	rs1554070777

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