ClinVar Miner

List of variants in gene TRPV4 reported as uncertain significance by GeneDx

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Total variants: 42
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HGVS dbSNP
NM_021625.4(TRPV4):c.1139C>T (p.Thr380Met) rs764949536
NM_021625.4(TRPV4):c.1184C>T (p.Thr395Met) rs374197231
NM_021625.4(TRPV4):c.1198C>T (p.Arg400Trp) rs781711282
NM_021625.4(TRPV4):c.1285G>A (p.Glu429Lys) rs879254080
NM_021625.4(TRPV4):c.1297G>A (p.Val433Met) rs879254304
NM_021625.4(TRPV4):c.1378C>T (p.Arg460Trp) rs34227547
NM_021625.4(TRPV4):c.1390C>T (p.Arg464Cys) rs373049874
NM_021625.4(TRPV4):c.1472A>G (p.Tyr491Cys) rs531738577
NM_021625.4(TRPV4):c.1492-1_1497delGCCGCCGinsCCT rs1555206481
NM_021625.4(TRPV4):c.1549A>G (p.Thr517Ala) rs1085307827
NM_021625.4(TRPV4):c.1885G>A (p.Ala629Thr) rs200838499
NM_021625.4(TRPV4):c.1912C>G (p.Pro638Ala) rs760044422
NM_021625.4(TRPV4):c.1913C>T (p.Pro638Leu) rs35058636
NM_021625.4(TRPV4):c.2198G>A (p.Trp733Ter) rs200757159
NM_021625.4(TRPV4):c.2236C>T (p.Arg746Cys) rs375189134
NM_021625.4(TRPV4):c.2387A>G (p.Asn796Ser) rs1188535536
NM_021625.4(TRPV4):c.2452C>T (p.Arg818Cys) rs776544875
NM_021625.4(TRPV4):c.2471C>T (p.Ser824Leu) rs764622721
NM_021625.4(TRPV4):c.2513C>T (p.Pro838Leu) rs140602150
NM_021625.4(TRPV4):c.2557_2586del30 (p.Cys853_Arg862del) rs1555204381
NM_021625.4(TRPV4):c.2560G>A (p.Asp854Asn) rs368963822
NM_021625.4(TRPV4):c.2584delC (p.Arg862Alafs) rs746597270
NM_021625.4(TRPV4):c.2585G>A (p.Arg862His) rs371989034
NM_021625.4(TRPV4):c.25C>T (p.Arg9Cys) rs758741868
NM_021625.4(TRPV4):c.2605G>A (p.Ala869Thr) rs138396764
NM_021625.4(TRPV4):c.281C>T (p.Ser94Leu) rs201927283
NM_021625.4(TRPV4):c.326A>G (p.Asp109Gly) rs1131691532
NM_021625.4(TRPV4):c.37G>A (p.Gly13Arg) rs763302555
NM_021625.4(TRPV4):c.37G>T (p.Gly13Trp) rs763302555
NM_021625.4(TRPV4):c.402C>A (p.Ser134Arg) rs201241092
NM_021625.4(TRPV4):c.478delC (p.Arg160Glyfs) rs1064796238
NM_021625.4(TRPV4):c.479G>A (p.Arg160Gln) rs139300843
NM_021625.4(TRPV4):c.569C>T (p.Thr190Met) rs1031096826
NM_021625.4(TRPV4):c.695G>A (p.Arg232His) rs769107613
NM_021625.4(TRPV4):c.704A>G (p.Tyr235Cys) rs754848195
NM_021625.4(TRPV4):c.709C>T (p.Arg237Ter) rs746368269
NM_021625.4(TRPV4):c.773T>C (p.Val258Ala) rs1555208102
NM_021625.4(TRPV4):c.830A>G (p.Asp277Gly) rs879254007
NM_021625.4(TRPV4):c.855G>T (p.Gly285=) rs879253959
NM_021625.4(TRPV4):c.898A>G (p.Ile300Val) rs114612488
NM_021625.4(TRPV4):c.914C>T (p.Thr305Met) rs754582307
NM_021625.4(TRPV4):c.956C>T (p.Ser319Leu) rs377518118

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