ClinVar Miner

List of variants in gene TRPV3 reported as benign for keratosis

Included ClinVar conditions (103):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_145068.4(TRPV3):c.73A>G (p.Ile25Val) rs322965 0.99860
NM_145068.3(TRPV3):c.-269A>G rs322958 0.67103
NM_145068.4(TRPV3):c.270G>A (p.Gln90=) rs1039519 0.59507
NM_145068.4(TRPV3):c.1923C>T (p.Asp641=) rs7216486 0.54548
NM_145068.4(TRPV3):c.558A>C (p.Ile186=) rs11078458 0.52296
NM_145068.4(TRPV3):c.936G>A (p.Thr312=) rs395357 0.43180
NM_145068.4(TRPV3):c.349A>G (p.Arg117Gly) rs322937 0.32171
NM_145068.4(TRPV3):c.224+27T>C rs9911213 0.31129
NM_145068.4(TRPV3):c.1878C>T (p.Ser626=) rs12946883 0.29746
NM_145068.3(TRPV3):c.-190G>A rs322959 0.26919
NM_145068.4(TRPV3):c.1066-46T>C rs4790510 0.26811
NM_145068.3(TRPV3):c.-142G>C rs11870904 0.10006
NM_145068.4(TRPV3):c.394G>A (p.Val132Met) rs8066242 0.06287
NM_145068.4(TRPV3):c.1419G>C (p.Leu473Phe) rs56169438 0.05871
NM_145068.4(TRPV3):c.1435A>T (p.Met479Leu) rs114131791 0.02536
NM_145068.4(TRPV3):c.1882G>A (p.Ala628Thr) rs75319568 0.01408
NM_145068.4(TRPV3):c.2278+10C>T rs112791047 0.01185
NM_145068.4(TRPV3):c.2331T>C (p.Asn777=) rs74362949 0.01019
NM_145068.4(TRPV3):c.224+8C>T rs113563330 0.00898
NM_145068.4(TRPV3):c.2321C>T (p.Thr774Ile) rs7212634 0.00712
NM_145068.4(TRPV3):c.2278+9G>A rs79589254 0.00538
NM_145068.4(TRPV3):c.1503+13C>G rs141061726 0.00458
NM_145068.4(TRPV3):c.807A>G (p.Ala269=) rs75487373 0.00413
NM_145068.4(TRPV3):c.*58C>T rs188455894 0.00363
NM_145068.3(TRPV3):c.-226G>C rs187117947 0.00306
NM_145068.4(TRPV3):c.1105C>T (p.Arg369Trp) rs116535534 0.00299
NM_145068.4(TRPV3):c.119+10G>A rs182566183 0.00255
NM_145068.4(TRPV3):c.2358G>T (p.Pro786=) rs75372730 0.00212
NM_145068.4(TRPV3):c.958A>G (p.Met320Val) rs142326624 0.00130
NM_145068.4(TRPV3):c.1698G>A (p.Thr566=) rs113716355 0.00125
NM_145068.4(TRPV3):c.72C>T (p.Ala24=) rs116068630 0.00088
NM_145068.4(TRPV3):c.1654G>A (p.Val552Met) rs150743616 0.00070
NM_145068.4(TRPV3):c.415C>T (p.Leu139=) rs150701364 0.00063
NM_145068.4(TRPV3):c.1050G>A (p.Lys350=) rs141575082 0.00058
NM_145068.4(TRPV3):c.852C>T (p.His284=) rs144990390 0.00038
NM_145068.4(TRPV3):c.1503+15C>T rs369415284 0.00037
NM_145068.4(TRPV3):c.2185C>T (p.Arg729Ter) rs11654533 0.00031
NM_145068.4(TRPV3):c.1504-15C>T rs200955758 0.00026
NM_145068.4(TRPV3):c.1401+4C>T rs367941175 0.00023
NM_145068.4(TRPV3):c.1236C>T (p.Asn412=) rs141578451 0.00021
NM_145068.4(TRPV3):c.1083C>T (p.Leu361=) rs193231694 0.00019
NM_145068.4(TRPV3):c.489G>A (p.Thr163=) rs771432151 0.00019
NM_145068.4(TRPV3):c.2034C>T (p.Gly678=) rs201663049 0.00018
NM_145068.3(TRPV3):c.-234C>T rs568432604 0.00017
NM_145068.4(TRPV3):c.1044C>T (p.Ala348=) rs139733808 0.00017
NM_145068.4(TRPV3):c.1258C>T (p.Leu420=) rs199598561 0.00017
NM_145068.4(TRPV3):c.1045G>A (p.Ala349Thr) rs146393183 0.00016
NM_145068.4(TRPV3):c.2078G>A (p.Arg693His) rs201062148 0.00007
NM_145068.4(TRPV3):c.395T>C (p.Val132Ala) rs139870087 0.00006
NM_145068.4(TRPV3):c.643+2T>C rs746570091 0.00006
NM_145068.4(TRPV3):c.955C>T (p.Arg319Cys) rs370662760 0.00005
NM_145068.4(TRPV3):c.1622T>C (p.Leu541Ser) rs764913664 0.00003
NM_145068.4(TRPV3):c.2235C>T (p.His745=) rs746226070 0.00003
NM_145068.4(TRPV3):c.784+11C>T rs757838946 0.00002
NM_145068.4(TRPV3):c.-2-8T>C rs762080322 0.00001
NM_145068.4(TRPV3):c.1078A>C (p.Ile360Leu) rs767689187 0.00001
NM_145068.4(TRPV3):c.1242C>T (p.Asp414=) rs779350392 0.00001
NM_145068.4(TRPV3):c.1427C>T (p.Thr476Met) rs766631634 0.00001
NM_145068.4(TRPV3):c.1065+16G>T rs454738
NM_145068.4(TRPV3):c.1281G>T (p.Thr427=) rs114034214
NM_145068.4(TRPV3):c.2279-15T>A rs72809877
NM_145068.4(TRPV3):c.592G>A (p.Asp198Asn) rs78615718
NM_145068.4(TRPV3):c.956G>A (p.Arg319His) rs151284467
NM_145068.4(TRPV3):c.95C>G (p.Ala32Gly) rs115770751

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.