ClinVar Miner

Variants in gene TRMU with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_018006.5(TRMU):c.*8G>C rs55905826
NM_018006.5(TRMU):c.272A>G (p.Lys91Arg) rs138044544
NM_018006.5(TRMU):c.387A>G (p.Ala129=) rs144586525
NM_018006.5(TRMU):c.772+8G>A rs201372242
NM_018006.5(TRMU):c.900G>T (p.Leu300=) rs113846383

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