ClinVar Miner

List of variants in gene combination SPATA22, TRPV3 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_145068.4(TRPV3):c.*1043T>C rs569015257 0.00057
NM_145068.4(TRPV3):c.*2757C>T rs760837552 0.00036
NM_145068.4(TRPV3):c.*3045G>T rs773007859 0.00029
NM_145068.4(TRPV3):c.*2432C>T rs779675543 0.00019
NM_145068.4(TRPV3):c.*2019A>G rs753994797 0.00014
NM_145068.4(TRPV3):c.*132G>C rs745761873 0.00011
NM_145068.4(TRPV3):c.*2808C>T rs190136323 0.00009
NM_145068.4(TRPV3):c.*1280G>A rs999273445 0.00007
NM_145068.4(TRPV3):c.*2490T>C rs886052842 0.00007
NM_145068.4(TRPV3):c.*752dup rs886052850 0.00007
NM_145068.4(TRPV3):c.*1940T>G rs886052845 0.00006
NM_145068.4(TRPV3):c.*207T>C rs1006630449 0.00006
NM_145068.4(TRPV3):c.*1218G>A rs886052848 0.00004
NM_145068.4(TRPV3):c.*1669G>A rs886052846 0.00004
NM_145068.4(TRPV3):c.*1380T>C rs943473331 0.00003
NM_145068.4(TRPV3):c.*3340C>G rs886052835 0.00003
NM_145068.4(TRPV3):c.*2702A>G rs187226946 0.00002
NM_145068.4(TRPV3):c.*74G>C rs886052854 0.00002
NM_145068.4(TRPV3):c.*1111G>C rs1443868171 0.00001
NM_145068.4(TRPV3):c.*1328C>A rs2074127690 0.00001
NM_145068.4(TRPV3):c.*1500C>T rs981157331 0.00001
NM_145068.4(TRPV3):c.*1968A>G rs1250351429 0.00001
NM_145068.4(TRPV3):c.*2391C>T rs2074113998 0.00001
NM_145068.4(TRPV3):c.*2622G>T rs886052841 0.00001
NM_145068.4(TRPV3):c.*2784G>T rs2074107131 0.00001
NM_145068.4(TRPV3):c.*2895C>G rs886052839 0.00001
NM_145068.4(TRPV3):c.*3148G>A rs886052838 0.00001
NM_145068.4(TRPV3):c.*85A>G rs886052853 0.00001
NM_001321336.2(SPATA22):c.-74+2923A>T rs911023444
NM_145068.4(TRPV3):c.*1105T>C rs2074131140
NM_145068.4(TRPV3):c.*1110TG[1] rs886052849
NM_145068.4(TRPV3):c.*1186C>T rs751104119
NM_145068.4(TRPV3):c.*1272C>T rs2074128477
NM_145068.4(TRPV3):c.*1590del rs869218825
NM_145068.4(TRPV3):c.*1591G>C rs5010536
NM_145068.4(TRPV3):c.*1591_*1592insC rs112072753
NM_145068.4(TRPV3):c.*1625C>G rs886052847
NM_145068.4(TRPV3):c.*1767T>C rs981104963
NM_145068.4(TRPV3):c.*1843C>T rs1043683273
NM_145068.4(TRPV3):c.*2054A>C rs554529243
NM_145068.4(TRPV3):c.*2296T>C rs886052844
NM_145068.4(TRPV3):c.*2365T>C rs886052843
NM_145068.4(TRPV3):c.*2671C>T rs886052840
NM_145068.4(TRPV3):c.*276C>T rs545675279
NM_145068.4(TRPV3):c.*3114C>A rs2074103145
NM_145068.4(TRPV3):c.*3295G>C rs886052837
NM_145068.4(TRPV3):c.*3302TG[5] rs886052836
NM_145068.4(TRPV3):c.*552C>A rs1259149909
NM_145068.4(TRPV3):c.*631A>G rs886052851
NM_145068.4(TRPV3):c.*837A>G rs758698680
NM_145068.4(TRPV3):c.*842A>G rs767061806
NM_145068.4(TRPV3):c.*92A>C rs886052852

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