ClinVar Miner

List of variants in gene TMC1 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 19
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NM_138691.2(TMC1):c.1019T>C (p.Met340Thr) rs111033464
NM_138691.2(TMC1):c.1070A>G (p.Asn357Ser) rs397517834
NM_138691.2(TMC1):c.1071C>T (p.Asn357=) rs1489881026
NM_138691.2(TMC1):c.1225-8C>T rs375785074
NM_138691.2(TMC1):c.1233G>A (p.Met411Ile) rs184603559
NM_138691.2(TMC1):c.1263A>G (p.Pro421=) rs139985214
NM_138691.2(TMC1):c.1566+8C>T rs202184917
NM_138691.2(TMC1):c.1567-4A>G rs369562300
NM_138691.2(TMC1):c.1602C>G (p.Thr534=) rs111033462
NM_138691.2(TMC1):c.2070G>A (p.Ala690=) rs145757452
NM_138691.2(TMC1):c.2178G>A (p.Ala726=) rs555517698
NM_138691.2(TMC1):c.483G>A (p.Glu161=) rs375984349
NM_138691.2(TMC1):c.684C>T (p.Thr228=) rs890529621
NM_138691.2(TMC1):c.760G>A (p.Val254Ile) rs111033497
NM_138691.2(TMC1):c.777T>C (p.Tyr259=) rs727503482
NM_138691.3(TMC1):c.342G>A (p.Glu114=)
NM_138691.3(TMC1):c.822G>A (p.Pro274=)
NM_138691.3(TMC1):c.951C>G (p.Val317=)

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