ClinVar Miner

List of variants in gene TRPV4 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP
NM_021625.4(TRPV4):c.*1G>A rs927502204
NM_021625.4(TRPV4):c.*8A>C rs751605215
NM_021625.4(TRPV4):c.1038C>T (p.Tyr346=) rs750086412
NM_021625.4(TRPV4):c.1062C>T (p.Ala354=) rs115446386
NM_021625.4(TRPV4):c.1104C>T (p.Asn368=) rs768593770
NM_021625.4(TRPV4):c.1107C>T (p.Asp369=) rs771626710
NM_021625.4(TRPV4):c.1116G>A (p.Ser372=) rs369811541
NM_021625.4(TRPV4):c.1134C>T (p.Ala378=) rs375468689
NM_021625.4(TRPV4):c.126G>A (p.Gly42=) rs1057523956
NM_021625.4(TRPV4):c.1278G>A (p.Thr426=) rs139179261
NM_021625.4(TRPV4):c.1284G>A (p.Gly428=) rs150773110
NM_021625.4(TRPV4):c.1308C>T (p.Ile436=) rs141244183
NM_021625.4(TRPV4):c.1337G>T (p.Arg446Leu) rs143502097
NM_021625.4(TRPV4):c.1392C>G (p.Arg464=) rs182609216
NM_021625.4(TRPV4):c.1398C>T (p.Phe466=) rs146929022
NM_021625.4(TRPV4):c.1434C>T (p.Tyr478=) rs749421876
NM_021625.4(TRPV4):c.143C>T (p.Ser48Leu) rs756185743
NM_021625.4(TRPV4):c.1464C>T (p.Thr488=) rs146841400
NM_021625.4(TRPV4):c.1479G>A (p.Pro493=) rs1337838267
NM_021625.4(TRPV4):c.1482G>A (p.Leu494=) rs143722984
NM_021625.4(TRPV4):c.1491+10C>T rs201815805
NM_021625.4(TRPV4):c.1491+8C>T rs752455441
NM_021625.4(TRPV4):c.1539C>T (p.Gly513=) rs141295418
NM_021625.4(TRPV4):c.1546A>G (p.Ile516Val) rs115976458
NM_021625.4(TRPV4):c.1581C>T (p.Thr527=) rs114653066
NM_021625.4(TRPV4):c.1584+12G>A rs375908611
NM_021625.4(TRPV4):c.1584+12G>T rs375908611
NM_021625.4(TRPV4):c.1584+13C>T rs199712027
NM_021625.4(TRPV4):c.1584+18G>A rs10850750
NM_021625.4(TRPV4):c.1584+18del rs757667255
NM_021625.4(TRPV4):c.1585-18C>T rs201974634
NM_021625.4(TRPV4):c.15C>T (p.Ser5=) rs751824781
NM_021625.4(TRPV4):c.1656del (p.Tyr553fs) rs541606391
NM_021625.4(TRPV4):c.1658+15C>T rs200083069
NM_021625.4(TRPV4):c.1713C>G (p.Ile571Met) rs185933892
NM_021625.4(TRPV4):c.1744C>T (p.Leu582=) rs35078611
NM_021625.4(TRPV4):c.1824+4C>T rs147259744
NM_021625.4(TRPV4):c.1825-14G>A rs114829048
NM_021625.4(TRPV4):c.1825-15C>G rs200602134
NM_021625.4(TRPV4):c.1825-15C>T rs200602134
NM_021625.4(TRPV4):c.1857C>T (p.Leu619=) rs781048658
NM_021625.4(TRPV4):c.1891+47C>T rs145460865
NM_021625.4(TRPV4):c.1892-13T>C rs1555205476
NM_021625.4(TRPV4):c.1892-9C>T rs376975164
NM_021625.4(TRPV4):c.2043C>T (p.Gly681=) rs375633647
NM_021625.4(TRPV4):c.2088C>T (p.Ile696=) rs367846257
NM_021625.4(TRPV4):c.2208+3G>A rs1057523473
NM_021625.4(TRPV4):c.2209-5C>T rs374184761
NM_021625.4(TRPV4):c.2226G>A (p.Leu742=) rs769329467
NM_021625.4(TRPV4):c.2248G>A (p.Val750Ile) rs148171058
NM_021625.4(TRPV4):c.2304G>A (p.Ser768=) rs138986228
NM_021625.4(TRPV4):c.2304G>C (p.Ser768=) rs138986228
NM_021625.4(TRPV4):c.2337-16G>A rs373195035
NM_021625.4(TRPV4):c.2388C>T (p.Asn796=) rs116685089
NM_021625.4(TRPV4):c.2458+15G>T rs372913114
NM_021625.4(TRPV4):c.2472G>A (p.Ser824=) rs149988106
NM_021625.4(TRPV4):c.2498A>G (p.Asn833Ser) rs116035946
NM_021625.4(TRPV4):c.2514G>A (p.Pro838=) rs576688961
NM_021625.4(TRPV4):c.2559C>T (p.Cys853=) rs139580010
NM_021625.4(TRPV4):c.2604C>T (p.Asp868=) rs111598467
NM_021625.4(TRPV4):c.28G>C (p.Ala10Pro) rs376436045
NM_021625.4(TRPV4):c.300G>A (p.Lys100=) rs370135765
NM_021625.4(TRPV4):c.330C>T (p.Tyr110=) rs777176504
NM_021625.4(TRPV4):c.386+26G>C rs368996776
NM_021625.4(TRPV4):c.396G>A (p.Pro132=) rs114101785
NM_021625.4(TRPV4):c.426G>A (p.Pro142=) rs145327152
NM_021625.4(TRPV4):c.57C>T (p.Pro19=) rs112408790
NM_021625.4(TRPV4):c.58G>A (p.Gly20Arg) rs764970185
NM_021625.4(TRPV4):c.649G>T (p.Ala217Ser) rs187864727
NM_021625.4(TRPV4):c.651G>A (p.Ala217=) rs371280831
NM_021625.4(TRPV4):c.690C>T (p.Pro230=) rs747822070
NM_021625.4(TRPV4):c.712+10C>T rs115657305
NM_021625.4(TRPV4):c.712+19C>A rs1057521014
NM_021625.4(TRPV4):c.713-13C>T rs1361037363
NM_021625.4(TRPV4):c.713-16C>T rs777854437
NM_021625.4(TRPV4):c.760G>A (p.Val254Met) rs143548402
NM_021625.4(TRPV4):c.769C>G (p.Leu257Val) rs56217500
NM_021625.4(TRPV4):c.792C>A (p.Val264=) rs867185488
NM_021625.4(TRPV4):c.854-4G>A rs371733585
NM_021625.4(TRPV4):c.871C>T (p.Leu291=) rs1057521414
NM_021625.4(TRPV4):c.903C>G (p.Val301=) rs748103823
NM_021625.4(TRPV4):c.957G>A (p.Ser319=) rs116698155

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