List of variants in gene MTOR reported as pathogenic for not provided

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_004958.4(MTOR):c.4184A>G (p.Lys1395Arg)
NM_004958.4(MTOR):c.4448G>A (p.Cys1483Tyr)	rs786205165
NM_004958.4(MTOR):c.4448G>T (p.Cys1483Phe)	rs786205165
NM_004958.4(MTOR):c.5395G>A (p.Glu1799Lys)	rs863225264
NM_004958.4(MTOR):c.5663T>G (p.Phe1888Cys)	rs869312666
NM_004958.4(MTOR):c.5930C>T (p.Thr1977Ile)	rs587777893
NM_004958.4(MTOR):c.6981G>A (p.Met2327Ile)	rs878855328
NM_004958.4(MTOR):c.7216G>A (p.Val2406Met)	rs1557739557
NM_004958.4(MTOR):c.7255G>A (p.Glu2419Lys)	rs587777900

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