"Genetic Services Laboratory, University of Chicago"[submitter] AND "A - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 210378	NM_001940.4(ATN1):c.408C>T (p.Tyr136=)	ATN1	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 210377	NM_001007026.1(ATN1):c.1462CAG[17] (p.Gln488[17])	ATN1, LOC109461484	Microsatellite (inframe_insertion)	Dentatorubral-pallidoluysian atrophy +2 more	GConflicting classifications of pathogenicity
Select item 210373	NM_001940.4(ATN1):c.1461A>G (p.Gln487=)	ATN1, LOC109461484	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 210374	NM_001940.4(ATN1):c.1469_1476del (p.Gln490fs)	ATN1, LOC109461484 (Q490fs)	Deletion (frameshift variant)	not specified	GUncertain significance
Select item 210375	NM_001940.4(ATN1):c.1471_1472insCAGCAG (p.Gln491delinsProAlaGlu)	ATN1, LOC109461484	Insertion (inframe_indel)	not specified	GLikely benign
Select item 210376	NM_001940.4(ATN1):c.1472_1476del (p.Gln491fs)	ATN1, LOC109461484 (Q491fs)	Deletion (frameshift variant)	not specified	GUncertain significance
Select item 128461	NM_001940.4(ATN1):c.1647G>A (p.Leu549=)	ATN1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 128462	NM_001940.4(ATN1):c.2430C>A (p.Arg810=)	ATN1	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar