List of variants in gene MTOR studied for carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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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.3026G>A (p.Arg1009Gln)	rs778855567	0.00003
NM_004958.4(MTOR):c.4379T>C (p.Leu1460Pro)	rs1057519779
NM_004958.4(MTOR):c.4447T>C (p.Cys1483Arg)	rs1057519914
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.4449C>G (p.Cys1483Trp)	rs1057519913
NM_004958.4(MTOR):c.6040G>A (p.Glu2014Lys)	rs1057519780
NM_004958.4(MTOR):c.6643T>A (p.Ser2215Thr)	rs1057519917
NM_004958.4(MTOR):c.6644C>A (p.Ser2215Tyr)	rs587777894
NM_004958.4(MTOR):c.6644C>T (p.Ser2215Phe)	rs587777894
NM_004958.4(MTOR):c.6667C>A (p.Gln2223Lys)	rs1057519778
NM_004958.4(MTOR):c.7255G>A (p.Glu2419Lys)	rs587777900
NM_004958.4(MTOR):c.7498A>T (p.Ile2500Phe)	rs1057519916
NM_004958.4(MTOR):c.7500T>G (p.Ile2500Met)	rs1057519915
NM_004958.4(MTOR):c.7514G>C (p.Arg2505Pro)	rs1057519777

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