List of variants in gene TSC2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.3422C>T (p.Ala1141Val)	rs34870424	0.00587
NM_000548.5(TSC2):c.4285G>T (p.Ala1429Ser)	rs45474795	0.00306
NM_000548.5(TSC2):c.275A>T (p.Glu92Val)	rs137853994	0.00101
NM_000548.5(TSC2):c.856A>G (p.Met286Val)	rs1800748	0.00083
NM_000548.5(TSC2):c.2476C>A (p.Leu826Met)	rs45517238	0.00073
NM_000548.5(TSC2):c.5131G>A (p.Val1711Met)	rs139779505	0.00054
NM_000548.5(TSC2):c.1512C>G (p.Val504=)	rs146359990	0.00035
NM_000548.5(TSC2):c.5116C>T (p.Arg1706Cys)	rs45517391	0.00029
NM_000548.5(TSC2):c.4105C>T (p.Arg1369Trp)	rs45517328	0.00026
NM_000548.5(TSC2):c.2295C>T (p.Ala765=)	rs45509500	0.00019
NM_000548.5(TSC2):c.3475C>T (p.Arg1159Trp)	rs45517295	0.00016
NM_000548.5(TSC2):c.4094C>T (p.Ser1365Leu)	rs377123510	0.00012
NM_000548.5(TSC2):c.3557A>G (p.Tyr1186Cys)	rs137854421	0.00011
NM_000548.5(TSC2):c.4225C>T (p.Arg1409Trp)	rs45517333	0.00005
NM_000548.5(TSC2):c.2887G>A (p.Val963Met)	rs45517275	0.00004
NM_000548.5(TSC2):c.4767G>A (p.Pro1589=)	rs769246304	0.00004
NM_000548.5(TSC2):c.5010C>T (p.His1670=)	rs376306544	0.00004
NM_000548.5(TSC2):c.1915C>T (p.Arg639Trp)	rs766451267	0.00003
NM_000548.5(TSC2):c.4849+18C>T	rs45517374	0.00002
NM_000548.5(TSC2):c.721G>A (p.Val241Ile)	rs200943828	0.00002
NM_000548.5(TSC2):c.1911C>T (p.Val637=)	rs543584836	0.00001
NM_000548.5(TSC2):c.2098-9T>C	rs755416873	0.00001
NM_000548.5(TSC2):c.362C>G (p.Ala121Gly)	rs767755750	0.00001
NM_000548.5(TSC2):c.3958G>A (p.Val1320Ile)	rs767495365	0.00001
NM_000548.5(TSC2):c.5343A>G (p.Pro1781=)	rs747614356	0.00001
NM_000548.5(TSC2):c.576C>T (p.Asp192=)	rs761704292	0.00001
NM_000548.5(TSC2):c.1422C>T (p.Leu474=)	rs565646854
NM_000548.5(TSC2):c.4524CTT[1] (p.Phe1510del)	rs137854239
NM_000548.5(TSC2):c.486C>T (p.Asp162=)	rs45473598

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