ClinVar Miner

List of variants in gene TRPV3 reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 61
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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.1878C>T (p.Ser626=) rs12946883 0.29746
NM_145068.3(TRPV3):c.-190G>A rs322959 0.26919
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.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

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