ClinVar Miner

Variants in gene MPI with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP gnomAD frequency
NM_002435.3(MPI):c.982C>T (p.Arg328Trp) rs117089191 0.00577
NM_002435.3(MPI):c.303C>T (p.Leu101=) rs139228075 0.00240
NM_002435.3(MPI):c.414G>A (p.Met138Ile) rs150217523 0.00227
NM_002435.3(MPI):c.10C>T (p.Pro4Ser) rs143982014 0.00133
NM_002435.3(MPI):c.1049C>T (p.Thr350Met) rs116933453 0.00095
NM_002435.3(MPI):c.214A>C (p.Ser72Arg) rs146699267 0.00031
NM_002435.3(MPI):c.1125G>A (p.Gly375=) rs552854858 0.00016

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