List of variants in gene MTOR reported as uncertain significance for not specified

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.889G>A (p.Asp297Asn)	rs141936187	0.00006
NM_004958.4(MTOR):c.1870C>T (p.Arg624Cys)	rs780398729	0.00004
NM_004958.4(MTOR):c.5570A>C (p.Glu1857Ala)	rs1643091373	0.00001
NM_004958.4(MTOR):c.2885A>G (p.Gln962Arg)	rs879255386
NM_004958.4(MTOR):c.3525C>G (p.Asp1175Glu)
NM_004958.4(MTOR):c.4687-3T>C	rs760066667
NM_004958.4(MTOR):c.4998+1G>A
NM_004958.4(MTOR):c.6247_6248insT (p.Glu2083fs)	rs1642875607
NM_004958.4(MTOR):c.7017-4A>G

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