List of variants in gene TRIO reported as likely pathogenic by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
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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_007118.4(TRIO):c.298C>T (p.Arg100Ter)
NM_007118.4(TRIO):c.3571C>T (p.Gln1191Ter)
NM_007118.4(TRIO):c.3657dup (p.Cys1220fs)	rs1554068529
NM_007118.4(TRIO):c.4394A>G (p.Asn1465Ser)	rs1747669042
NM_007118.4(TRIO):c.6153+1G>A	rs1755124330
NM_007118.4(TRIO):c.651_652del (p.Arg217fs)	rs1736840999
NM_007118.4(TRIO):c.6554_6557del (p.Glu2185fs)	rs2126611738

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