ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 13
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HGVS dbSNP
NM_002435.3(MPI):c.1050G>A (p.Thr350=) rs145431554
NM_002435.3(MPI):c.10C>T (p.Pro4Ser) rs143982014
NM_002435.3(MPI):c.1212C>T (p.Val404=)
NM_002435.3(MPI):c.1269G>A (p.Leu423=) rs371664469
NM_002435.3(MPI):c.132G>A (p.Lys44=) rs778577329
NM_002435.3(MPI):c.303C>T (p.Leu101=) rs139228075
NM_002435.3(MPI):c.378G>A (p.Pro126=) rs752948071
NM_002435.3(MPI):c.573C>T (p.Ala191=) rs200903491
NM_002435.3(MPI):c.670+9A>T rs7495739
NM_002435.3(MPI):c.671-4T>G rs199719453
NM_002435.3(MPI):c.845-10G>C rs748693066
NM_002435.3(MPI):c.849C>T (p.Cys283=) rs377419930
NM_002435.3(MPI):c.855G>A (p.Glu285=) rs769504650

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