ClinVar Miner

List of variants in gene MVK reported as uncertain significance

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Total variants: 115
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HGVS dbSNP
NM_000431.4(MVK):c.*125G>T
NM_000431.4(MVK):c.*308G>A rs886048935
NM_000431.4(MVK):c.*332C>T rs574536495
NM_000431.4(MVK):c.*333G>A
NM_000431.4(MVK):c.*358G>A
NM_000431.4(MVK):c.*431C>T rs72648044
NM_000431.4(MVK):c.*468C>T rs768794506
NM_000431.4(MVK):c.*486C>T
NM_000431.4(MVK):c.*550G>A rs886048936
NM_000431.4(MVK):c.*566G>C
NM_000431.4(MVK):c.*571G>A
NM_000431.4(MVK):c.*601G>A rs536969522
NM_000431.4(MVK):c.*75T>G rs138924471
NM_000431.4(MVK):c.-15G>A rs567278499
NM_000431.4(MVK):c.-33G>A rs886048930
NM_000431.4(MVK):c.-55G>C rs886048929
NM_000431.4(MVK):c.1005C>T (p.Gly335=) rs104895357
NM_000431.4(MVK):c.1051C>T (p.Pro351Ser) rs773929129
NM_000431.4(MVK):c.1055A>C (p.Glu352Ala)
NM_000431.4(MVK):c.1067C>T (p.Thr356Met) rs104895342
NM_000431.4(MVK):c.1073A>C (p.Gln358Pro)
NM_000431.4(MVK):c.1096G>C (p.Asp366His) rs1566153793
NM_000431.4(MVK):c.1126G>A (p.Gly376Ser)
NM_000431.4(MVK):c.1129G>A (p.Val377Ile) rs28934897
NM_000431.4(MVK):c.1139A>G (p.His380Arg) rs104895324
NM_000431.4(MVK):c.1163G>A (p.Arg388Gln) rs886048934
NM_000431.4(MVK):c.1174G>A (p.Ala392Thr)
NM_000431.4(MVK):c.1175C>T (p.Ala392Val)
NM_000431.4(MVK):c.1189T>C (p.Ter397Arg) rs1555279757
NM_000431.4(MVK):c.119G>A (p.Arg40Gln) rs373095009
NM_000431.4(MVK):c.14T>C (p.Val5Ala) rs141765653
NM_000431.4(MVK):c.151C>T (p.Leu51Phe) rs892779197
NM_000431.4(MVK):c.155G>T (p.Ser52Ile)
NM_000431.4(MVK):c.166A>G (p.Ile56Val) rs149095003
NM_000431.4(MVK):c.178C>T (p.Arg60Trp)
NM_000431.4(MVK):c.187G>A (p.Asp63Asn)
NM_000431.4(MVK):c.226+4A>G rs145732290
NM_000431.4(MVK):c.227-18T>C rs876661049
NM_000431.4(MVK):c.227A>G (p.Glu76Gly) rs1593015412
NM_000431.4(MVK):c.238G>A (p.Val80Ile) rs76914224
NM_000431.4(MVK):c.244A>G (p.Thr82Ala)
NM_000431.4(MVK):c.254C>T (p.Ser85Leu)
NM_000431.4(MVK):c.258G>A (p.Glu86=)
NM_000431.4(MVK):c.277_283del (p.Glu93fs) rs104895369
NM_000431.4(MVK):c.287G>T (p.Gly96Val) rs1337856151
NM_000431.4(MVK):c.298G>A (p.Asp100Asn)
NM_000431.4(MVK):c.29C>T (p.Ala10Val)
NM_000431.4(MVK):c.302G>A (p.Cys101Tyr) rs886048931
NM_000431.4(MVK):c.317G>A (p.Arg106His) rs778337320
NM_000431.4(MVK):c.32C>T (p.Pro11Leu) rs876661001
NM_000431.4(MVK):c.331G>A (p.Ala111Thr) rs371257609
NM_000431.4(MVK):c.33G>A (p.Pro11=)
NM_000431.4(MVK):c.349C>G (p.Leu117Val)
NM_000431.4(MVK):c.361C>T (p.Arg121Trp)
NM_000431.4(MVK):c.368A>T (p.Gln123Leu)
NM_000431.4(MVK):c.36G>T (p.Gly12=)
NM_000431.4(MVK):c.371+13T>C rs201201471
NM_000431.4(MVK):c.371+1GT[4] rs1337419856
NM_000431.4(MVK):c.371+4T>C
NM_000431.4(MVK):c.37A>C (p.Lys13Gln)
NM_000431.4(MVK):c.394G>A (p.Val132Ile) rs104895336
NM_000431.4(MVK):c.413C>T (p.Pro138Leu)
NM_000431.4(MVK):c.441C>T (p.Ala147=) rs138342076
NM_000431.4(MVK):c.449C>T (p.Ser150Leu)
NM_000431.4(MVK):c.484G>A (p.Glu162Lys) rs200457031
NM_000431.4(MVK):c.498C>A (p.Asn166Lys) rs765975337
NM_000431.4(MVK):c.503_508del (p.Leu168_Asp170delinsHis)
NM_000431.4(MVK):c.511G>A (p.Gly171Arg) rs104895337
NM_000431.4(MVK):c.512G>A (p.Gly171Glu)
NM_000431.4(MVK):c.518G>A (p.Cys173Tyr) rs1267793765
NM_000431.4(MVK):c.520G>A (p.Val174Ile)
NM_000431.4(MVK):c.524A>G (p.Asn175Ser)
NM_000431.4(MVK):c.527+10G>A rs368909134
NM_000431.4(MVK):c.527+13C>A rs199670546
NM_000431.4(MVK):c.527+8T>C rs377547988
NM_000431.4(MVK):c.565G>T (p.Ala189Ser)
NM_000431.4(MVK):c.591C>T (p.His197=) rs104895329
NM_000431.4(MVK):c.592G>A (p.Gly198Arg)
NM_000431.4(MVK):c.595A>T (p.Asn199Tyr) rs1566147301
NM_000431.4(MVK):c.598C>T (p.Pro200Ser) rs886048932
NM_000431.4(MVK):c.614A>G (p.Asn205Ser) rs767853272
NM_000431.4(MVK):c.631+3A>G
NM_000431.4(MVK):c.632-3del
NM_000431.4(MVK):c.653A>C (p.Gln218Pro)
NM_000431.4(MVK):c.663T>G (p.Ile221Met) rs757289914
NM_000431.4(MVK):c.678-3C>A
NM_000431.4(MVK):c.681G>A (p.Ser227=)
NM_000431.4(MVK):c.719C>G (p.Pro240Arg) rs1458254066
NM_000431.4(MVK):c.722G>A (p.Arg241His)
NM_000431.4(MVK):c.724A>G (p.Asn242Asp)
NM_000431.4(MVK):c.752G>A (p.Arg251Lys)
NM_000431.4(MVK):c.755A>G (p.Asn252Ser)
NM_000431.4(MVK):c.775G>A (p.Glu259Lys)
NM_000431.4(MVK):c.78+8G>A rs766391278
NM_000431.4(MVK):c.785C>T (p.Ala262Val) rs763106439
NM_000431.4(MVK):c.787C>T (p.Pro263Ser)
NM_000431.4(MVK):c.799T>C (p.Ser267Pro)
NM_000431.4(MVK):c.802A>G (p.Ile268Val) rs759997079
NM_000431.4(MVK):c.80T>G (p.Val27Gly)
NM_000431.4(MVK):c.819G>A (p.Leu273=) rs876661134
NM_000431.4(MVK):c.832G>A (p.Val278Met) rs574045811
NM_000431.4(MVK):c.857C>T (p.Pro286Leu) rs104895379
NM_000431.4(MVK):c.863C>T (p.Pro288Leu) rs104895355
NM_000431.4(MVK):c.870G>T (p.Gln290His)
NM_000431.4(MVK):c.874C>T (p.Leu292Phe) rs145586352
NM_000431.4(MVK):c.876C>T (p.Leu292=) rs370301290
NM_000431.4(MVK):c.877G>A (p.Val293Met) rs104895356
NM_000431.4(MVK):c.889C>A (p.Leu297Ile)
NM_000431.4(MVK):c.904C>T (p.Gln302Ter) rs886048933
NM_000431.4(MVK):c.924C>T (p.Leu308=) rs72648042
NM_000431.4(MVK):c.936C>T (p.His312=) rs1212639017
NM_000431.4(MVK):c.937G>A (p.Ala313Thr) rs371789705
NM_000431.4(MVK):c.945G>A (p.Leu315=) rs752469036
NM_000431.4(MVK):c.961G>A (p.Val321Met) rs779869991
NM_000431.4(MVK):c.974G>A (p.Arg325His) rs374686559

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