ClinVar Miner

Submissions for variant NM_002839.4(PTPRD):c.5692C>T (p.Arg1898Cys)

gnomAD frequency: 0.00001  dbSNP: rs150063446
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Science for Life laboratory, Karolinska Institutet RCV000149336 SCV000088978 unknown Malignant tumor of prostate no assertion criteria provided not provided Converted during submission to Uncertain significance.

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