ClinVar Miner

List of variants in gene TUSC3 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_006765.4(TUSC3):c.*1665T>C rs562496423 0.00707
NM_006765.4(TUSC3):c.*1581C>T rs182976372 0.00571
NM_006765.4(TUSC3):c.*1078C>G rs146010253 0.00523
NM_006765.4(TUSC3):c.*2397G>A rs141748006 0.00400
NM_006765.4(TUSC3):c.*1009C>A rs529522962 0.00336
NM_006765.4(TUSC3):c.*1197G>A rs142084453 0.00272
NM_006765.4(TUSC3):c.-82A>G rs528698301 0.00203
NM_006765.4(TUSC3):c.*1191C>T rs577607900 0.00199
NM_006765.3(TUSC3):c.-190C>T rs573872013 0.00184
NM_006765.4(TUSC3):c.*2241T>C rs149848404 0.00147
NM_006765.4(TUSC3):c.*1957A>G rs182645260 0.00128
NM_006765.4(TUSC3):c.*1531A>G rs190430215 0.00112
NM_006765.4(TUSC3):c.*1024T>C rs537908016 0.00096
NM_006765.4(TUSC3):c.*589G>A rs188770392 0.00091
NM_006765.4(TUSC3):c.*2393A>G rs536605918 0.00083
NM_006765.4(TUSC3):c.*732G>A rs765219222 0.00071
NM_006765.4(TUSC3):c.937+11G>C rs371792364 0.00064
NM_006765.4(TUSC3):c.38C>T (p.Ala13Val) rs200808372 0.00054
NM_006765.4(TUSC3):c.*1723T>G rs537999024 0.00050
NM_006765.4(TUSC3):c.*98A>G rs112569707 0.00047
NM_006765.4(TUSC3):c.*1371T>G rs749833807 0.00041
NM_006765.4(TUSC3):c.*1391T>C rs573563224 0.00040
NM_006765.4(TUSC3):c.*222A>G rs571116375 0.00031
NM_006765.4(TUSC3):c.768T>C (p.Tyr256=) rs149033081 0.00029
NM_006765.4(TUSC3):c.*2183G>A rs187586489 0.00026
NM_006765.4(TUSC3):c.568-15A>G rs186717319 0.00018
NM_006765.4(TUSC3):c.*1313G>A rs560586222 0.00014
NM_006765.4(TUSC3):c.-46G>C rs749998335 0.00013
NM_006765.3(TUSC3):c.-206C>T rs886062763 0.00011
NM_006765.4(TUSC3):c.*947A>G rs963702307 0.00011
NM_006765.4(TUSC3):c.*2363G>T rs554105159 0.00010
NM_006765.4(TUSC3):c.*763A>C rs539187664 0.00010
NM_006765.4(TUSC3):c.-130C>G rs886062770 0.00010
NM_006765.4(TUSC3):c.*2101A>G rs151122954 0.00009
NM_006765.4(TUSC3):c.*2283T>C rs960356882 0.00008
NM_006765.3(TUSC3):c.-303C>G rs886062761 0.00006
NM_006765.3(TUSC3):c.-304G>T rs886062760 0.00006
NM_006765.4(TUSC3):c.*1607T>C rs146317430 0.00006
NM_006765.4(TUSC3):c.*499G>A rs1321556219 0.00006
NM_006765.4(TUSC3):c.-48C>T rs750899051 0.00006
NM_006765.4(TUSC3):c.25C>G (p.Arg9Gly) rs755808199 0.00006
NM_006765.4(TUSC3):c.934C>T (p.Arg312Trp) rs554205458 0.00006
NM_006765.4(TUSC3):c.*188C>T rs923246673 0.00005
NM_006765.4(TUSC3):c.*2037G>C rs775550670 0.00004
NM_006765.4(TUSC3):c.*605C>G rs749903402 0.00004
NM_006765.4(TUSC3):c.852T>C (p.Ile284=) rs781741877 0.00004
NM_006765.4(TUSC3):c.426+15C>T rs574008930 0.00003
NM_006765.4(TUSC3):c.677A>G (p.Tyr226Cys) rs146409575 0.00003
NM_006765.4(TUSC3):c.-51G>A rs779146487 0.00002
NM_006765.4(TUSC3):c.*217C>T rs1201787189 0.00001
NM_006765.4(TUSC3):c.*2277A>G rs936557459 0.00001
NM_006765.4(TUSC3):c.*2371C>T rs1270490406 0.00001
NM_006765.4(TUSC3):c.*288G>A rs781373100 0.00001
NM_006765.4(TUSC3):c.-150C>T rs886062769 0.00001
NM_006765.4(TUSC3):c.17C>T (p.Ala6Val) rs1211304490 0.00001
NM_006765.4(TUSC3):c.259A>G (p.Ile87Val) rs759296891 0.00001
NM_006765.4(TUSC3):c.408G>A (p.Gly136=) rs762831751 0.00001
NM_006765.4(TUSC3):c.843A>G (p.Ser281=) rs202151515 0.00001
NM_001413669.1(TUSC3):c.-30-83007A>G rs1801621217
NM_006765.3(TUSC3):c.-175_-174CT[1] rs761637643
NM_006765.3(TUSC3):c.-191C>T rs886062765
NM_006765.3(TUSC3):c.-197_-195TCT[1] rs886062764
NM_006765.3(TUSC3):c.-254C>A rs775641863
NM_006765.3(TUSC3):c.-289A>G rs886062762
NM_006765.4(TUSC3):c.*111G>A rs557579844
NM_006765.4(TUSC3):c.*128A>G rs1812266668
NM_006765.4(TUSC3):c.*1737C>T rs886062773
NM_006765.4(TUSC3):c.*1861A>G rs1812315835
NM_006765.4(TUSC3):c.*1973T>A rs1812318856
NM_006765.4(TUSC3):c.*2010dup rs886062774
NM_006765.4(TUSC3):c.*2057T>C rs959992574
NM_006765.4(TUSC3):c.*2131G>T rs1812323628
NM_006765.4(TUSC3):c.*2146A>T rs886062775
NM_006765.4(TUSC3):c.*2316A>G rs1812329333
NM_006765.4(TUSC3):c.*2407G>A rs888651565
NM_006765.4(TUSC3):c.*286C>G rs14732
NM_006765.4(TUSC3):c.*341A>G rs1812272965
NM_006765.4(TUSC3):c.*364G>C rs111425809
NM_006765.4(TUSC3):c.*36T>G rs1374192276
NM_006765.4(TUSC3):c.*510C>A rs141126690
NM_006765.4(TUSC3):c.*566G>A rs536053560
NM_006765.4(TUSC3):c.*686A>C rs1812284354
NM_006765.4(TUSC3):c.*869A>C rs886062772
NM_006765.4(TUSC3):c.-111C>A rs1479784219
NM_006765.4(TUSC3):c.-159C>T rs886062768
NM_006765.4(TUSC3):c.-167G>A rs886062767
NM_006765.4(TUSC3):c.189C>G (p.Arg63=) rs751317981
NM_006765.4(TUSC3):c.23C>T (p.Ser8Leu) rs1420153973
NM_006765.4(TUSC3):c.3G>A (p.Met1Ile) rs886062771
NM_006765.4(TUSC3):c.414del (p.Asp138fs) rs1563154271
NM_006765.4(TUSC3):c.426+13A>T rs757683053
NM_006765.4(TUSC3):c.482A>G (p.Lys161Arg) rs1807328725
NM_006765.4(TUSC3):c.62C>G (p.Pro21Arg) rs750727769
NM_006765.4(TUSC3):c.838G>A (p.Glu280Lys) rs1810684992

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