ClinVar Miner

List of variants in gene TG reported as uncertain significance for not provided

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.7755-9T>G rs190979363 0.00473
NM_003235.5(TG):c.4484T>C (p.Val1495Ala) rs61740825 0.00330
NM_003235.5(TG):c.6200-7T>A rs79724982 0.00240
NM_003235.5(TG):c.6181G>A (p.Gly2061Arg) rs115436575 0.00198
NM_003235.5(TG):c.3999C>G (p.Ile1333Met) rs150728539 0.00134
NM_003235.5(TG):c.848G>A (p.Arg283Gln) rs146926250 0.00073
NM_003235.5(TG):c.229G>A (p.Gly77Ser) rs142698837 0.00071
NM_003235.5(TG):c.455G>A (p.Arg152His) rs114781869 0.00059
NM_003235.5(TG):c.4481C>T (p.Pro1494Leu) rs146498231 0.00052
NM_003235.5(TG):c.3139+9G>A rs201582196 0.00048
NM_003235.5(TG):c.4527C>T (p.His1509=) rs201216611 0.00039
NM_003235.5(TG):c.8026C>T (p.Arg2676Trp) rs114613744 0.00038
NM_003235.5(TG):c.6001G>A (p.Asp2001Asn) rs199923962 0.00037
NM_003235.5(TG):c.6605C>G (p.Pro2202Arg) rs150133670 0.00035
NM_003235.5(TG):c.8147C>T (p.Ser2716Phe) rs115574138 0.00029
NM_003235.5(TG):c.3985G>A (p.Gly1329Ser) rs192226069 0.00025
NM_003235.5(TG):c.4378G>A (p.Val1460Ile) rs199615848 0.00019
NM_003235.5(TG):c.4638C>T (p.Gly1546=) rs116663504 0.00018
NM_003235.5(TG):c.6191A>G (p.Gln2064Arg) rs143645885 0.00017
NM_003235.5(TG):c.2560C>T (p.Arg854Trp) rs202196940 0.00016
NM_003235.5(TG):c.4268G>A (p.Arg1423His) rs146594373 0.00013
NM_003235.5(TG):c.4990G>A (p.Val1664Met) rs180705321 0.00011
NM_003235.5(TG):c.6769G>A (p.Ala2257Thr) rs199683856 0.00008
NM_003235.5(TG):c.3149G>T (p.Trp1050Leu) rs142124591 0.00007
NM_003235.5(TG):c.4093A>T (p.Asn1365Tyr) rs142264604 0.00007
NM_003235.5(TG):c.554C>T (p.Ala185Val) rs142432006 0.00006
NM_003235.5(TG):c.3835C>T (p.Arg1279Trp) rs368926894 0.00004
NM_003235.5(TG):c.6304G>C (p.Val2102Leu) rs1022412169 0.00003
NM_003235.5(TG):c.7239+4A>C rs763128813 0.00003
NM_003235.5(TG):c.6707C>T (p.Pro2236Leu) rs145564745 0.00002
NM_003235.5(TG):c.217G>A (p.Val73Met) rs780845778 0.00001
NM_003235.5(TG):c.3176T>C (p.Ile1059Thr) rs1016185504 0.00001
NM_003235.5(TG):c.3856C>A (p.Leu1286Met) rs1064796627 0.00001
NM_003235.5(TG):c.5835G>C (p.Gln1945His) rs1244764731 0.00001
NM_003235.5(TG):c.1775C>T (p.Ala592Val)
NM_003235.5(TG):c.1890A>T (p.Gln630His)
NM_003235.5(TG):c.2639C>G (p.Pro880Arg)
NM_003235.5(TG):c.275G>T (p.Cys92Phe) rs1313276149
NM_003235.5(TG):c.3196C>T (p.Arg1066Cys)
NM_003235.5(TG):c.3367G>A (p.Gly1123Ser) rs1057524360
NM_003235.5(TG):c.3491G>T (p.Gly1164Val) rs760317901
NM_003235.5(TG):c.3638C>A (p.Pro1213Gln) rs754194585
NM_003235.5(TG):c.3652_3653delinsAT (p.Pro1218Ile) rs2132331772
NM_003235.5(TG):c.3727C>G (p.Gln1243Glu)
NM_003235.5(TG):c.3836G>A (p.Arg1279Gln)
NM_003235.5(TG):c.3847+1G>C
NM_003235.5(TG):c.4474C>T (p.Pro1492Ser)
NM_003235.5(TG):c.4777G>T (p.Val1593Phe) rs1053887198
NM_003235.5(TG):c.506GTC[1] (p.Arg170del) rs2132059579
NM_003235.5(TG):c.5447A>G (p.Gln1816Arg)
NM_003235.5(TG):c.5690G>A (p.Cys1897Tyr) rs121912649
NM_003235.5(TG):c.5906C>T (p.Pro1969Leu)
NM_003235.5(TG):c.6131G>T (p.Arg2044Leu) rs573866267
NM_003235.5(TG):c.6370T>C (p.Ser2124Pro)
NM_003235.5(TG):c.6397G>C (p.Glu2133Gln)
NM_003235.5(TG):c.6619G>A (p.Gly2207Ser)
NM_003235.5(TG):c.665G>A (p.Ser222Asn) rs1814693797
NM_003235.5(TG):c.6783-8A>G rs780817859
NM_003235.5(TG):c.7165G>C (p.Ala2389Pro) rs765477121
NM_003235.5(TG):c.8137G>A (p.Ala2713Thr)
NM_003235.5(TG):c.8237C>T (p.Thr2746Met)

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