ClinVar Miner

List of variants in gene TMC1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_138691.3(TMC1):c.-219A>G rs7026304 0.55869
NM_138691.3(TMC1):c.-468G>A rs7022441 0.53167
NM_138691.3(TMC1):c.236+216T>C rs2589614 0.51877
NM_138691.3(TMC1):c.45C>T (p.Asp15=) rs2589615 0.51851
NM_138691.3(TMC1):c.-305-67G>A rs10217204 0.49983
NM_138691.3(TMC1):c.2261-13G>T rs115008515 0.41445
NM_138691.3(TMC1):c.362+100T>C rs7046504 0.32826
NM_138691.3(TMC1):c.2260+306C>A rs4330753 0.32033
NM_138691.3(TMC1):c.535+201A>G rs2793171 0.22165
NM_138691.3(TMC1):c.535+101A>G rs7848136 0.22130
NM_138691.3(TMC1):c.241G>A (p.Glu81Lys) rs1796993 0.21988
NM_138691.3(TMC1):c.535+74G>A rs12345051 0.14748
NM_138691.3(TMC1):c.-329C>A rs7856724 0.13978
NM_138691.3(TMC1):c.16+94T>G rs1444842 0.10653
NM_138691.3(TMC1):c.1764-168T>C rs12002855 0.09630
NM_138691.3(TMC1):c.1764-319G>A rs12001653 0.09630
NM_138691.3(TMC1):c.1566+169G>C rs72733079 0.09501
NM_138691.3(TMC1):c.1029+85T>C rs55846842 0.09096
NM_138691.3(TMC1):c.1713C>T (p.Phe571=) rs34532421 0.08866
NM_138691.3(TMC1):c.1763+123G>A rs56349532 0.08858
NM_138691.3(TMC1):c.1225-276A>G rs75047732 0.08856
NM_138691.3(TMC1):c.1567-67T>A rs7860172 0.08697
NM_138691.3(TMC1):c.2208+49C>T rs13286809 0.08377
NM_138691.3(TMC1):c.643-169A>T rs13285034 0.06466
NM_138691.3(TMC1):c.1695+289A>G rs199694514 0.06358
NM_138691.3(TMC1):c.16+190C>T rs34872646 0.05154
NM_138691.3(TMC1):c.-540C>T rs112220638 0.02586
NM_138691.3(TMC1):c.*183A>G rs71507808 0.02514
NM_138691.3(TMC1):c.884+318A>G rs74782211 0.02131
NM_138691.3(TMC1):c.1404+50C>T rs74517917 0.01848
NM_138691.3(TMC1):c.1457T>C (p.Met486Thr) rs17058153 0.01664
NM_138691.3(TMC1):c.*106G>C rs79830675 0.01140
NM_138691.3(TMC1):c.*28A>C rs151157872 0.00779
NM_138691.3(TMC1):c.-275G>A rs58824091 0.00773
NM_138691.3(TMC1):c.421C>T (p.Arg141Trp) rs11143384 0.00691
NM_138691.3(TMC1):c.2260+3_2260+5del rs546307383 0.00308
NM_138691.3(TMC1):c.1404+16G>A rs189532643 0.00254
NM_138691.3(TMC1):c.2004-46C>T rs141086229 0.00102
NM_138691.3(TMC1):c.1566+8C>T rs202184917 0.00059
NM_138691.3(TMC1):c.696C>T (p.Ala232=) rs112843964 0.00047
NM_138691.3(TMC1):c.822G>A (p.Pro274=) rs370523728 0.00016
NM_138691.3(TMC1):c.795A>C (p.Thr265=) rs140398130 0.00013
NM_138691.3(TMC1):c.760G>A (p.Val254Ile) rs111033497 0.00009
NM_138691.3(TMC1):c.2129+15T>A rs747921456 0.00008
NM_138691.3(TMC1):c.*156T>C rs545955592 0.00005
NM_138691.3(TMC1):c.*262dup rs71495343
NM_138691.3(TMC1):c.-195-11del rs36038786
NM_138691.3(TMC1):c.1695+102T>G rs35431794
NM_138691.3(TMC1):c.1695+36del rs111880209
NM_138691.3(TMC1):c.1695+36dup rs111880209
NM_138691.3(TMC1):c.1763+20G>A
NM_138691.3(TMC1):c.2209-10dup
NM_138691.3(TMC1):c.2261-15C>T rs200393712
NM_138691.3(TMC1):c.238GAA[3] (p.Glu83del) rs376040866
NM_138691.3(TMC1):c.362+101_362+102insTACA rs1242969553
NM_138691.3(TMC1):c.362+119AC[10] rs10645769
NM_138691.3(TMC1):c.362+119AC[11] rs10645769
NM_138691.3(TMC1):c.362+71AT[11] rs72200654
NM_138691.3(TMC1):c.362+71AT[13] rs72200654
NM_138691.3(TMC1):c.362+71AT[14] rs72200654
NM_138691.3(TMC1):c.362+71AT[16] rs72200654
NM_138691.3(TMC1):c.362+84_362+123del rs71359517
NM_138691.3(TMC1):c.535+103AAAC[3] rs146170244
NM_138691.3(TMC1):c.535+219G>A rs2793172
NM_138691.3(TMC1):c.65-316G>A rs1663742
NM_138691.3(TMC1):c.741+187_741+188del rs368423344
NM_138691.3(TMC1):c.741+188GA[10] rs55848138
NM_138691.3(TMC1):c.741+188GA[11] rs55848138
NM_138691.3(TMC1):c.741+188GA[12] rs55848138
NM_138691.3(TMC1):c.741+188GA[14] rs55848138
NM_138691.3(TMC1):c.741+212_741+217del rs756603110

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.