List of variants in gene ATIC reported as uncertain significance for perceptual disorders

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004044.7(ATIC):c.1751A>G (p.His584Arg)	rs201429123	0.00011
NM_004044.7(ATIC):c.548C>A (p.Ala183Glu)	rs761526509	0.00002
NM_004044.7(ATIC):c.1474G>T (p.Asp492Tyr)	rs771474223	0.00001
NM_004044.7(ATIC):c.131delinsGCA (p.Ala44fs)
NM_004044.7(ATIC):c.1466A>G (p.Asn489Ser)
NM_004044.7(ATIC):c.406G>A (p.Ala136Thr)	rs1575116846
NM_004044.7(ATIC):c.794del (p.Phe265fs)	rs754173354

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