ClinVar Miner

Submissions for variant NM_001007228.2(SPOP):c.399C>G (p.Phe133Leu)

dbSNP: rs193921065
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Science for Life laboratory, Karolinska Institutet RCV000149021 SCV000088663 unknown Malignant tumor of prostate no assertion criteria provided not provided Converted during submission to Uncertain significance.
Database of Curated Mutations (DoCM) RCV000435302 SCV000507423 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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