List of variants in gene MTOR reported as 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004958.4(MTOR):c.5126G>A (p.Arg1709His)	rs587777895	0.00002
NM_004958.4(MTOR):c.3541G>A (p.Val1181Ile)	rs1274311146	0.00001
NM_004958.4(MTOR):c.6875A>G (p.Asn2292Ser)	rs374052581	0.00001
NM_004958.4(MTOR):c.5902C>T (p.His1968Tyr)	rs1057519870
NM_004958.4(MTOR):c.5930C>A (p.Thr1977Lys)	rs587777893
NM_004958.4(MTOR):c.6637C>T (p.Pro2213Ser)	rs1057519871
NM_004958.4(MTOR):c.6644C>T (p.Ser2215Phe)	rs587777894
NM_004958.4(MTOR):c.6674dup (p.Tyr2225Ter)	rs1642559236
NM_004958.4(MTOR):c.7255G>A (p.Glu2419Lys)	rs587777900
NM_004958.4(MTOR):c.7391G>T (p.Gly2464Val)	rs1641758308
NM_004958.4(MTOR):c.7576G>A (p.Glu2526Lys)	rs1641671309

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