ClinVar Miner

List of variants in gene TMC1 reported as likely benign for not specified

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Total variants: 25
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HGVS dbSNP
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.135C>A (p.Thr45=) rs111353632
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.2129+15T>A
NM_138691.2(TMC1):c.2178G>A (p.Ala726=) rs555517698
NM_138691.2(TMC1):c.2260+3_2260+5del rs546307383
NM_138691.2(TMC1):c.238_240GAA[3] (p.Glu83del) rs376040866
NM_138691.2(TMC1):c.342G>A
NM_138691.2(TMC1):c.421C>T (p.Arg141Trp) rs11143384
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.742-12G>A rs886038723
NM_138691.2(TMC1):c.760G>A (p.Val254Ile) rs111033497
NM_138691.2(TMC1):c.777T>C (p.Tyr259=) rs727503482
NM_138691.2(TMC1):c.795A>C (p.Thr265=) rs140398130
NM_138691.2(TMC1):c.822G>A
NM_138691.2(TMC1):c.951C>G

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