ClinVar Miner

List of variants in gene THRB reported as likely benign

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001354712.2(THRB):c.*4611del rs147687234 0.01502
NM_001354712.2(THRB):c.*1372C>A rs147542176 0.00081
NM_001354712.2(THRB):c.1125C>T (p.Ala375=) rs148991421 0.00033
NM_001354712.2(THRB):c.11A>G (p.Asn4Ser) rs114070375 0.00028
NM_001354712.2(THRB):c.1299C>T (p.Ala433=) rs144206187 0.00024
NM_001354712.2(THRB):c.161C>T (p.Ser54Leu) rs141731067 0.00018
NM_001354712.2(THRB):c.159G>C (p.Gln53His) rs567722846 0.00016
NM_001354712.2(THRB):c.213C>A (p.Asp71Glu) rs141495471 0.00016
NM_001354712.2(THRB):c.283+12T>C rs372413180 0.00013
NM_001354712.2(THRB):c.1053C>T (p.Asp351=) rs115445992 0.00011
NM_001354712.2(THRB):c.*4714T>C rs577889185 0.00009
NM_001354712.2(THRB):c.68G>A (p.Arg23Gln) rs200124942 0.00009
NM_001354712.2(THRB):c.40T>C (p.Trp14Arg) rs777353759 0.00007
NM_001354712.2(THRB):c.129A>T (p.Ser43=) rs112913751 0.00004
NM_001354712.2(THRB):c.175A>G (p.Ile59Val) rs141172732 0.00003
NM_001354712.2(THRB):c.*1861A>G rs529916834 0.00002
NM_001354712.2(THRB):c.75C>T (p.His25=) rs760778175 0.00001
NM_001354712.2(THRB):c.*1750del rs147125300
NM_001354712.2(THRB):c.*1776dup rs536659624
NM_001354712.2(THRB):c.*2572ATTG[3] rs144580659
NM_001354712.2(THRB):c.*3324dup rs35554555
NM_001354712.2(THRB):c.*570dup rs569875966
NM_001354712.2(THRB):c.*900del rs373141874
NM_001354712.2(THRB):c.22+4T>A rs1031696535
NM_001354712.2(THRB):c.284-12625C>G

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