ClinVar Miner

List of variants in gene MPI reported as uncertain significance for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP gnomAD frequency
NM_002435.3(MPI):c.303C>T (p.Leu101=) rs139228075 0.00240
NM_002435.3(MPI):c.10C>T (p.Pro4Ser) rs143982014 0.00133
NM_002435.3(MPI):c.670+11T>C rs144118442 0.00046
NM_002435.3(MPI):c.1050G>A (p.Thr350=) rs145431554 0.00026
NM_002435.3(MPI):c.671-4T>G rs199719453 0.00025
NM_002435.3(MPI):c.573C>T (p.Ala191=) rs200903491 0.00022
NM_002435.3(MPI):c.1178G>C (p.Gly393Ala) rs201815588 0.00019
NM_002435.3(MPI):c.1139G>A (p.Ser380Asn) rs141660799 0.00015
NM_002435.3(MPI):c.378G>A (p.Pro126=) rs752948071 0.00011
NM_002435.3(MPI):c.662C>G (p.Ser221Cys) rs760911969 0.00010
NM_002435.3(MPI):c.748G>A (p.Gly250Ser) rs748090636 0.00010
NM_002435.3(MPI):c.167G>A (p.Arg56Gln) rs200452019 0.00009
NM_002435.3(MPI):c.818A>G (p.Asn273Ser) rs150525282 0.00009
NM_002435.3(MPI):c.-5C>T rs145533697 0.00008
NM_002435.3(MPI):c.849C>T (p.Cys283=) rs377419930 0.00007
NM_002435.3(MPI):c.1269G>A (p.Leu423=) rs371664469 0.00006
NM_002435.3(MPI):c.61A>G (p.Met21Val) rs376746368 0.00006
NM_002435.3(MPI):c.132G>A (p.Lys44=) rs778577329 0.00005
NM_002435.3(MPI):c.*93C>T rs1336372205 0.00004
NM_002435.3(MPI):c.1053+15A>G rs564765063 0.00004
NM_002435.3(MPI):c.1053+3G>T rs753145834 0.00004
NM_002435.3(MPI):c.1175G>A (p.Arg392His) rs762164813 0.00004
NM_002435.3(MPI):c.1232C>T (p.Pro411Leu) rs147817691 0.00004
NM_002435.3(MPI):c.*44T>G rs774547352 0.00003
NM_002435.3(MPI):c.121G>A (p.Ala41Thr) rs779821212 0.00003
NM_002435.3(MPI):c.*109T>C rs905180827 0.00002
NM_002435.3(MPI):c.1064C>T (p.Ser355Phe) rs763169640 0.00002
NM_002435.3(MPI):c.739G>A (p.Gly247Ser) rs557366025 0.00002
NM_002435.3(MPI):c.1122G>C (p.Gln374His) rs753458883 0.00001
NM_002435.3(MPI):c.1156A>T (p.Thr386Ser) rs769768397 0.00001
NM_002435.3(MPI):c.1174C>T (p.Arg392Cys) rs751962765 0.00001
NM_002435.3(MPI):c.145-11T>C rs768029221 0.00001
NM_002435.3(MPI):c.1A>G (p.Met1Val) rs528828174 0.00001
NM_002435.3(MPI):c.472G>A (p.Val158Ile) rs886051482 0.00001
NM_002435.3(MPI):c.628G>A (p.Val210Met) rs781158335 0.00001
NM_002435.3(MPI):c.746T>C (p.Ile249Thr) rs201676072 0.00001
NM_002435.3(MPI):c.7G>A (p.Ala3Thr) rs770421382 0.00001
NM_002435.3(MPI):c.855G>A (p.Glu285=) rs769504650 0.00001
NM_002435.3(MPI):c.902A>G (p.Lys301Arg) rs534508637 0.00001
NM_002435.3(MPI):c.992A>C (p.Glu331Ala) rs1223295146 0.00001
NM_002435.3(MPI):c.*103T>C rs2064845890
NM_002435.3(MPI):c.*129G>C rs80226376
NM_002435.3(MPI):c.*176G>A rs886051484
NM_002435.3(MPI):c.*203G>A rs562995056
NM_002435.3(MPI):c.*205G>T rs2064847544
NM_002435.3(MPI):c.1023del (p.Val342fs) rs1555479441
NM_002435.3(MPI):c.1032C>G (p.Asp344Glu) rs2064831979
NM_002435.3(MPI):c.1053+6_1053+9del rs1279545559
NM_002435.3(MPI):c.1054-34_1054-11del rs1555479532
NM_002435.3(MPI):c.1054del rs752976348
NM_002435.3(MPI):c.1061G>A (p.Gly354Asp)
NM_002435.3(MPI):c.1069A>G (p.Thr357Ala) rs2064840019
NM_002435.3(MPI):c.1086G>A (p.Leu362=) rs905233208
NM_002435.3(MPI):c.1096T>C (p.Ser366Pro) rs1555479551
NM_002435.3(MPI):c.1157C>T (p.Thr386Ile) rs2141209748
NM_002435.3(MPI):c.1207A>T (p.Ser403Cys)
NM_002435.3(MPI):c.1212C>T (p.Val404=) rs2064843052
NM_002435.3(MPI):c.124G>C (p.Glu42Gln)
NM_002435.3(MPI):c.1260C>A (p.Cys420Ter) rs1555479632
NM_002435.3(MPI):c.140C>G (p.Ala47Gly)
NM_002435.3(MPI):c.170G>T (p.Gly57Val)
NM_002435.3(MPI):c.183_184delinsAA (p.Leu62Ile)
NM_002435.3(MPI):c.194G>A (p.Arg65His)
NM_002435.3(MPI):c.238G>A (p.Asp80Asn) rs1444877183
NM_002435.3(MPI):c.33T>G (p.Cys11Trp) rs2064708840
NM_002435.3(MPI):c.362T>C (p.Leu121Pro)
NM_002435.3(MPI):c.445T>C (p.Cys149Arg) rs2064746068
NM_002435.3(MPI):c.455G>C (p.Arg152Pro) rs766458792
NM_002435.3(MPI):c.45G>C (p.Gln15His) rs371649838
NM_002435.3(MPI):c.527C>T (p.Ala176Val) rs1256364766
NM_002435.3(MPI):c.530C>T (p.Thr177Ile)
NM_002435.3(MPI):c.533A>C (p.His178Pro) rs2141200350
NM_002435.3(MPI):c.587G>A (p.Ser196Asn)
NM_002435.3(MPI):c.602T>C (p.Leu201Pro) rs2064752971
NM_002435.3(MPI):c.661T>A (p.Ser221Thr)
NM_002435.3(MPI):c.670+3G>A
NM_002435.3(MPI):c.670+9A>T rs7495739
NM_002435.3(MPI):c.672G>C (p.Ala224=) rs768186349
NM_002435.3(MPI):c.678C>A (p.Ala226=) rs199972529
NM_002435.3(MPI):c.695A>G (p.Asp232Gly) rs765912695
NM_002435.3(MPI):c.781A>G (p.Thr261Ala) rs2064816825
NM_002435.3(MPI):c.793G>A (p.Gly265Arg) rs2064817105
NM_002435.3(MPI):c.796G>A (p.Glu266Lys) rs1595822583
NM_002435.3(MPI):c.843_844+1del
NM_002435.3(MPI):c.845-10G>C rs748693066
NM_002435.3(MPI):c.845-9T>C
NM_002435.3(MPI):c.914T>A (p.Val305Glu)
NM_002435.3(MPI):c.920C>G (p.Thr307Ser)
NM_002435.3(MPI):c.952_957del (p.Ser318_Ser319del) rs1555479384
NM_002435.3(MPI):c.95C>T (p.Ala32Val) rs1596440893
NM_002435.3(MPI):c.991del (p.Glu331fs) rs1555479423
NM_002435.3(MPI):c.995A>T (p.Asp332Val)

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