ClinVar Miner

List of variants in gene TSHR reported as benign for not provided

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000369.5(TSHR):c.2181G>C (p.Glu727Asp) rs1991517 0.90865
NM_000369.5(TSHR):c.*1152T>A rs2288494 0.85456
NM_000369.5(TSHR):c.*245C>T rs7144481 0.85116
NM_000369.5(TSHR):c.692+163A>G rs3783942 0.63598
NM_000369.5(TSHR):c.692+209C>A rs3783941 0.62312
NM_000369.5(TSHR):c.243-158T>C rs11159490 0.45393
NM_000369.5(TSHR):c.*1417T>C rs2288496 0.39155
NM_000369.5(TSHR):c.*1222G>C rs2288495 0.39107
NM_000369.5(TSHR):c.171-80T>A rs17111401 0.33276
NM_000369.5(TSHR):c.*431T>C rs17630128 0.26762
NM_000369.5(TSHR):c.546-175A>G rs2075178 0.26597
NM_000369.5(TSHR):c.561T>C (p.Asn187=) rs2075179 0.26593
NM_000369.5(TSHR):c.468-69C>T rs2075176 0.26363
NM_000369.5(TSHR):c.545+13A>G rs2241119 0.26331
NM_000369.5(TSHR):c.393-134G>T rs10147011 0.25196
NM_000369.5(TSHR):c.545+269G>A rs2075177 0.22241
NM_000369.5(TSHR):c.*172C>A rs2268477 0.16427
NM_000369.5(TSHR):c.*909C>T rs2288493 0.15203
NM_000369.5(TSHR):c.392+245A>G rs2075173 0.09038
NM_000369.5(TSHR):c.2232C>G (p.Asn744Lys) rs61743974 0.01750
NM_000369.5(TSHR):c.881+3A>G rs186091357 0.00298
NM_000369.5(TSHR):c.171-11T>C rs145265345 0.00266
NM_000369.5(TSHR):c.1935G>A (p.Leu645=) rs115815771 0.00247
NM_000369.5(TSHR):c.357T>A (p.Pro119=) rs144084915 0.00168
NM_000369.5(TSHR):c.2007T>C (p.Leu669=) rs148214091 0.00122
NM_000369.5(TSHR):c.1971C>T (p.Ser657=) rs143773384 0.00116
NM_000369.5(TSHR):c.1572C>G (p.Thr524=) rs144170635 0.00113
NM_000369.5(TSHR):c.2124G>T (p.Gly708=) rs145012289 0.00101
NM_000369.5(TSHR):c.2161G>T (p.Val721Phe) rs61745409 0.00035
NM_000369.5(TSHR):c.915T>A (p.Ser305Arg) rs142122217 0.00007
NM_000369.5(TSHR):c.1377G>A (p.Ala459=) rs113951800
NM_000369.5(TSHR):c.242+12del
NM_000369.5(TSHR):c.242+12dup
NM_000369.5(TSHR):c.393-12dup
NM_000369.5(TSHR):c.614+217GT[17] rs147149121
NM_000369.5(TSHR):c.614+68T>G
NM_000369.5(TSHR):c.692+20G>C

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