ClinVar Miner

List of variants in gene MCM4 reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_005914.3(MCM4):c.-253C>T rs17334305 0.02181
NM_005914.3(MCM4):c.-205C>T rs17287526 0.00226
NM_182746.3(MCM4):c.1406G>C (p.Ser469Thr) rs117063344 0.00202
NM_182746.3(MCM4):c.*842G>A rs17287781 0.00196
NM_182746.3(MCM4):c.961C>T (p.Arg321Cys) rs142732823 0.00188
NM_182746.3(MCM4):c.*387T>C rs144432703 0.00116
NM_182746.3(MCM4):c.*56G>A rs375801965 0.00108
NM_182746.3(MCM4):c.2102G>A (p.Arg701Gln) rs143417982 0.00078
NM_182746.3(MCM4):c.*955A>G rs529512295 0.00059
NM_182746.3(MCM4):c.848T>C (p.Ile283Thr) rs149232439 0.00053
NM_182746.3(MCM4):c.487A>G (p.Lys163Glu) rs34206069 0.00049
NM_182746.3(MCM4):c.*255A>G rs544019622 0.00040
NM_182746.3(MCM4):c.-68G>T rs17287533 0.00029
NM_182746.3(MCM4):c.*882G>A rs576678949 0.00026
NM_182746.3(MCM4):c.1175-7C>T rs372261482 0.00022
NM_182746.3(MCM4):c.*1134A>C rs11553127 0.00021
NM_182746.3(MCM4):c.2257G>C (p.Val753Leu) rs150870761 0.00021
NM_182746.3(MCM4):c.240C>T (p.Ile80=) rs148927296 0.00017
NM_182746.3(MCM4):c.*453A>G rs945047640 0.00015
NM_182746.3(MCM4):c.*109T>C rs1019587652 0.00014
NM_182746.3(MCM4):c.1829G>A (p.Arg610His) rs151044076 0.00013
NM_182746.3(MCM4):c.899A>G (p.Gln300Arg) rs144012681 0.00011
NM_182746.3(MCM4):c.*877G>A rs184913079 0.00007
NM_182746.3(MCM4):c.*315G>A rs751753458 0.00006
NM_005914.3(MCM4):c.-347C>A rs886062970 0.00005
NM_182746.3(MCM4):c.*1266G>A rs539412503 0.00005
NM_182746.3(MCM4):c.*357A>C rs1049961235 0.00005
NM_182746.3(MCM4):c.891C>T (p.Pro297=) rs148576543 0.00005
NM_182746.3(MCM4):c.*850T>A rs148413389 0.00004
NM_182746.3(MCM4):c.859G>A (p.Gly287Ser) rs751016435 0.00004
NM_182746.3(MCM4):c.*438A>G rs886062981 0.00003
NM_182746.3(MCM4):c.*443G>A rs552183222 0.00003
NM_182746.3(MCM4):c.-74C>T rs559247482 0.00003
NM_182746.3(MCM4):c.1264C>T (p.Arg422Trp) rs78091557 0.00003
NM_182746.3(MCM4):c.1973A>G (p.Tyr658Cys) rs771448184 0.00003
NM_182746.3(MCM4):c.811A>G (p.Met271Val) rs764420223 0.00003
NM_182746.3(MCM4):c.1661G>A (p.Arg554Lys) rs921501374 0.00002
NM_182746.3(MCM4):c.1784C>T (p.Thr595Ile) rs375753142 0.00002
NM_182746.3(MCM4):c.693G>A (p.Gln231=) rs557349481 0.00002
NM_182746.3(MCM4):c.159C>T (p.Thr53=) rs775056163 0.00001
NM_182746.3(MCM4):c.187G>T (p.Ala63Ser) rs886062974 0.00001
NM_182746.3(MCM4):c.199G>A (p.Val67Met) rs755044869 0.00001
NM_182746.3(MCM4):c.2020G>A (p.Glu674Lys) rs748923159 0.00001
NM_182746.3(MCM4):c.2101C>T (p.Arg701Trp) rs767399226 0.00001
NM_182746.3(MCM4):c.2296C>T (p.Arg766Trp) rs149597772 0.00001
NM_182746.3(MCM4):c.241C>T (p.Pro81Ser) rs886062975 0.00001
NM_182746.3(MCM4):c.253G>T (p.Asp85Tyr) rs760802348 0.00001
NM_182746.3(MCM4):c.440G>A (p.Gly147Asp) rs886062976 0.00001
NM_182746.3(MCM4):c.589C>T (p.Leu197Phe) rs1349008800 0.00001
NM_182746.3(MCM4):c.604G>A (p.Val202Ile) rs748499898 0.00001
NM_182746.3(MCM4):c.693+7A>G rs755216810 0.00001
NM_182746.3(MCM4):c.715A>G (p.Met239Val) rs752863422 0.00001
NM_182746.3(MCM4):c.940C>T (p.Arg314Trp) rs750729954 0.00001
NM_182746.3(MCM4):c.99C>T (p.Pro33=) rs199890906 0.00001
NM_005914.3(MCM4):c.-320dup rs532945813
NM_182746.3(MCM4):c.*1140G>A rs2091015101
NM_182746.3(MCM4):c.*1234T>C rs1219129728
NM_182746.3(MCM4):c.*125A>G rs886062979
NM_182746.3(MCM4):c.*213C>T rs886062980
NM_182746.3(MCM4):c.*37C>T rs1265494155
NM_182746.3(MCM4):c.*484del rs886062982
NM_182746.3(MCM4):c.*537T>C rs568975576
NM_182746.3(MCM4):c.-77G>A rs921147935
NM_182746.3(MCM4):c.1097C>T (p.Thr366Ile) rs756135528
NM_182746.3(MCM4):c.1103A>C (p.His368Pro) rs2090910060
NM_182746.3(MCM4):c.1419T>G (p.His473Gln) rs755120277
NM_182746.3(MCM4):c.1511T>C (p.Ile504Thr) rs2090944031
NM_182746.3(MCM4):c.1578C>G (p.Leu526=) rs34157149
NM_182746.3(MCM4):c.1578C>T (p.Leu526=) rs34157149
NM_182746.3(MCM4):c.157A>G (p.Thr53Ala) rs200598421
NM_182746.3(MCM4):c.1728C>T (p.Phe576=) rs148525401
NM_182746.3(MCM4):c.1844C>G (p.Ala615Gly) rs886062978
NM_182746.3(MCM4):c.2012A>G (p.Tyr671Cys) rs991671311
NM_182746.3(MCM4):c.2341G>A (p.Val781Met) rs765226208
NM_182746.3(MCM4):c.235+4C>G rs749639468
NM_182746.3(MCM4):c.2531T>C (p.Leu844Pro) rs1208915343
NM_182746.3(MCM4):c.311G>A (p.Arg104Lys) rs1563830466
NM_182746.3(MCM4):c.502-8A>G rs2090856775
NM_182746.3(MCM4):c.686dup (p.Tyr229Ter) rs1563831163
NM_182746.3(MCM4):c.732CTT[1] (p.Phe246del)
NM_182746.3(MCM4):c.978T>C (p.Ser326=) rs886062977

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