ClinVar Miner

List of variants in gene MEFV reported as uncertain significance for not provided

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Gene type:
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Total variants: 91
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HGVS dbSNP
NM_000243.2(MEFV):c.1016C>T (p.Ser339Phe) rs104895157
NM_000243.2(MEFV):c.1035A>T (p.Ser345=) rs1064797207
NM_000243.2(MEFV):c.1043G>A (p.Arg348His) rs104895198
NM_000243.2(MEFV):c.1061G>A (p.Arg354Gln) rs763015849
NM_000243.2(MEFV):c.1066C>G (p.Gln356Glu) rs377754606
NM_000243.2(MEFV):c.1105C>T (p.Pro369Ser) rs11466023
NM_000243.2(MEFV):c.116G>A (p.Arg39Lys) rs141288548
NM_000243.2(MEFV):c.1171G>A (p.Asp391Asn) rs764274816
NM_000243.2(MEFV):c.1223G>A (p.Arg408Gln) rs11466024
NM_000243.2(MEFV):c.1245C>T (p.Val415=) rs104895195
NM_000243.2(MEFV):c.124C>T (p.Arg42Trp) rs61754767
NM_000243.2(MEFV):c.1318C>G (p.Gln440Glu) rs11466026
NM_000243.2(MEFV):c.1337A>C (p.Glu446Ala) rs749651486
NM_000243.2(MEFV):c.1341G>C (p.Lys447Asn) rs756322372
NM_000243.2(MEFV):c.1370C>T (p.Ala457Val) rs104895151
NM_000243.2(MEFV):c.1382G>A (p.Arg461Gln) rs145637617
NM_000243.2(MEFV):c.1406T>C (p.Val469Ala) rs778686119
NM_000243.2(MEFV):c.1440dup (p.Val481fs) rs1085307581
NM_000243.2(MEFV):c.1587+33C>G rs146820856
NM_000243.2(MEFV):c.1587+7G>A rs375555497
NM_000243.2(MEFV):c.1622T>C (p.Val541Ala) rs922232615
NM_000243.2(MEFV):c.1772T>C (p.Ile591Thr) rs11466045
NM_000243.2(MEFV):c.1776C>T (p.Gly592=) rs104895161
NM_000243.2(MEFV):c.1779T>A (p.Ala593=) rs377657099
NM_000243.2(MEFV):c.1795A>G (p.Asn599Asp) rs104895210
NM_000243.2(MEFV):c.1886dup (p.Pro630fs) rs876660997
NM_000243.2(MEFV):c.18T>A (p.Ser6Arg) rs772221366
NM_000243.2(MEFV):c.1957C>T (p.Arg653Cys) rs375716505
NM_000243.2(MEFV):c.195C>T (p.Tyr65=) rs104895077
NM_000243.2(MEFV):c.198C>T (p.Ala66=) rs149380763
NM_000243.2(MEFV):c.2033G>A (p.Gly678Glu) rs104895088
NM_000243.2(MEFV):c.2084A>G rs104895094
NM_000243.2(MEFV):c.2141C>T (p.Pro714Leu) rs758628487
NM_000243.2(MEFV):c.2146A>G (p.Lys716Glu) rs746092199
NM_000243.2(MEFV):c.2227T>C (p.Phe743Leu) rs876661026
NM_000243.2(MEFV):c.2230G>T rs61732874
NM_000243.2(MEFV):c.2246C>G (p.Ser749Cys) rs104895171
NM_000243.2(MEFV):c.2271C>T (p.Ser757=) rs772754956
NM_000243.2(MEFV):c.2292G>T (p.Gly764=) rs142352887
NM_000243.2(MEFV):c.2314A>G (p.Ile772Val) rs104895163
NM_000243.2(MEFV):c.2338C>A (p.Pro780Thr) rs104895154
NM_000243.2(MEFV):c.233A>G (p.Asn78Ser) rs145015653
NM_000243.2(MEFV):c.233A>T (p.Asn78Ile) rs145015653
NM_000243.2(MEFV):c.282T>G (p.Tyr94Ter) rs762535762
NM_000243.2(MEFV):c.289C>A (p.Gln97Lys) rs747515115
NM_000243.2(MEFV):c.297C>T (p.Asn99=) rs104895175
NM_000243.2(MEFV):c.307G>C (p.Asp103His) rs757543348
NM_000243.2(MEFV):c.322A>C (p.Ser108Arg) rs104895103
NM_000243.2(MEFV):c.329T>C (p.Leu110Pro) rs11466018
NM_000243.2(MEFV):c.331G>A (p.Gly111Arg) rs112739451
NM_000243.2(MEFV):c.343C>A (p.Pro115Thr) rs147557169
NM_000243.2(MEFV):c.359C>T (p.Thr120Ile) rs772698222
NM_000243.2(MEFV):c.365A>G (p.Asp122Gly) rs876660988
NM_000243.2(MEFV):c.369C>A (p.His123Gln) rs587783379
NM_000243.2(MEFV):c.372C>T (p.Pro124=) rs104895078
NM_000243.2(MEFV):c.401C>A (p.Pro134Gln) rs377250147
NM_000243.2(MEFV):c.407G>A (p.Gly136Glu) rs876660989
NM_000243.2(MEFV):c.414_415delinsGT (p.Ala139Ser) rs1567237666
NM_000243.2(MEFV):c.427_442dup (p.Glu148fs) rs876660992
NM_000243.2(MEFV):c.436C>T (p.Gln146Ter) rs876660990
NM_000243.2(MEFV):c.439C>G (p.Pro147Ala) rs876660991
NM_000243.2(MEFV):c.442G>C (p.Glu148Gln) rs3743930
NM_000243.2(MEFV):c.443A>T (p.Glu148Val) rs104895076
NM_000243.2(MEFV):c.452G>C (p.Arg151Thr) rs886043273
NM_000243.2(MEFV):c.460T>C (p.Ser154Pro) rs756975501
NM_000243.2(MEFV):c.487G>C (p.Glu163Gln) rs759918824
NM_000243.2(MEFV):c.489G>T (p.Glu163Asp) rs759997694
NM_000243.2(MEFV):c.501G>C (p.Glu167Asp) rs104895079
NM_000243.2(MEFV):c.511G>A (p.Ala171Thr) rs876660993
NM_000243.2(MEFV):c.515A>C (p.Gln172Pro) rs104895211
NM_000243.2(MEFV):c.532C>T (p.Arg178Trp) rs1555459404
NM_000243.2(MEFV):c.547C>A (p.Pro183Thr) rs202196752
NM_000243.2(MEFV):c.577G>A (p.Ala193Thr) rs876660994
NM_000243.2(MEFV):c.585G>A (p.Glu195=) rs200766991
NM_000243.2(MEFV):c.586G>T (p.Gly196Trp) rs104895179
NM_000243.2(MEFV):c.621C>T (p.Ala207=) rs767667206
NM_000243.2(MEFV):c.657C>T (p.Gly219=) rs104895182
NM_000243.2(MEFV):c.688G>A (p.Glu230Lys) rs104895080
NM_000243.2(MEFV):c.744T>C (p.Ser248=) rs750362154
NM_000243.2(MEFV):c.775A>G (p.Ile259Val) rs104895144
NM_000243.2(MEFV):c.796A>G (p.Lys266Glu) rs755178462
NM_000243.2(MEFV):c.818C>T (p.Ser273Leu) rs483353019
NM_000243.2(MEFV):c.848C>G (p.Pro283Arg) rs104895119
NM_000243.2(MEFV):c.866C>T (p.Ala289Val) rs104895132
NM_000243.2(MEFV):c.910G>A (p.Gly304Arg) rs75977701
NM_000243.2(MEFV):c.926C>T (p.Thr309Met) rs104895155
NM_000243.2(MEFV):c.932C>T (p.Ala311Val) rs74346519
NM_000243.2(MEFV):c.941_942delinsAT (p.Arg314His) rs1085307824
NM_000243.2(MEFV):c.959G>C (p.Gly320Ala) rs374412819
NM_000243.2(MEFV):c.97G>T (p.Val33Leu) rs11466016
NM_000243.2(MEFV):c.986G>A (p.Arg329His) rs104895112

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