ClinVar Miner

List of variants in gene MPZ reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_000530.8(MPZ):c.*1048A>T rs71639057
NM_000530.8(MPZ):c.*195G>T rs150182811
NM_000530.8(MPZ):c.*1C>T
NM_000530.8(MPZ):c.*52G>A rs774701563
NM_000530.8(MPZ):c.*568C>G rs60731755
NM_000530.8(MPZ):c.*624C>T rs60821801
NM_000530.8(MPZ):c.*743C>T rs140992541
NM_000530.8(MPZ):c.-34_-17del rs1553260024
NM_000530.8(MPZ):c.-49C>A rs750777955
NM_000530.8(MPZ):c.102C>T (p.Thr34=) rs749600926
NM_000530.8(MPZ):c.114C>G (p.Val38=) rs1571820275
NM_000530.8(MPZ):c.174C>T (p.Val58=)
NM_000530.8(MPZ):c.200G>A (p.Arg67His) rs201720099
NM_000530.8(MPZ):c.201C>T (p.Arg67=) rs1571819920
NM_000530.8(MPZ):c.210C>T (p.Pro70=) rs545129173
NM_000530.8(MPZ):c.211G>A (p.Glu71Lys) rs573007540
NM_000530.8(MPZ):c.235-7C>T rs1057522724
NM_000530.8(MPZ):c.24C>T (p.Ser8=) rs144841836
NM_000530.8(MPZ):c.270C>T (p.Asp90=)
NM_000530.8(MPZ):c.297C>T (p.Ile99=) rs770430402
NM_000530.8(MPZ):c.354C>T (p.Asp118=) rs780896055
NM_000530.8(MPZ):c.372G>A (p.Thr124=) rs536830537
NM_000530.8(MPZ):c.384C>T (p.Asp128=) rs772611598
NM_000530.8(MPZ):c.417C>T (p.Thr139=) rs1571818696
NM_000530.8(MPZ):c.42G>A (p.Leu14=)
NM_000530.8(MPZ):c.483G>C (p.Val161=) rs769244921
NM_000530.8(MPZ):c.504G>A (p.Val168=) rs145592910
NM_000530.8(MPZ):c.51G>A (p.Leu17=) rs149637045
NM_000530.8(MPZ):c.531C>T (p.Tyr177=)
NM_000530.8(MPZ):c.584+10G>C rs946514874
NM_000530.8(MPZ):c.585-5T>C rs1026836999
NM_000530.8(MPZ):c.585-8T>C rs1571817654
NM_000530.8(MPZ):c.637G>C (p.Gly213Arg) rs202176679
NM_000530.8(MPZ):c.645+10A>G
NM_000530.8(MPZ):c.645+12T>C rs750848798
NM_000530.8(MPZ):c.646-7C>G rs377495735
NM_000530.8(MPZ):c.646-7C>T rs377495735
NM_000530.8(MPZ):c.648G>T (p.Thr216=) rs755728895
NM_000530.8(MPZ):c.654G>A (p.Val218=) rs1571817228
NM_000530.8(MPZ):c.655C>T (p.Leu219=) rs1571817225
NM_000530.8(MPZ):c.684C>T (p.Ser228=) rs34307129
NM_000530.8(MPZ):c.708G>A (p.Lys236=) rs768913825
NM_000530.8(MPZ):c.738T>C (p.Asp246=) rs1571816986
NM_000530.8(MPZ):c.77C>T (p.Pro26Leu) rs530923760
NM_000530.8(MPZ):c.78G>C (p.Pro26=) rs777790314

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