Variants in gene PCLO 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: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_033026.6(PCLO):c.1297G>A (p.Ala433Thr)	rs201344475	0.00180
NM_033026.6(PCLO):c.13840G>A (p.Ala4614Thr)	rs117222461	0.00125
NM_033026.6(PCLO):c.7571A>T (p.Gln2524Leu)	rs201409874	0.00052
NM_033026.6(PCLO):c.8483C>T (p.Thr2828Ile)	rs189352647	0.00033
NM_033026.6(PCLO):c.8458A>G (p.Met2820Val)	rs149645551	0.00009
NM_033026.6(PCLO):c.7868T>G (p.Val2623Gly)	rs776949129	0.00007
NM_033026.6(PCLO):c.929C>G (p.Thr310Ser)	rs377435737	0.00006
NM_033026.6(PCLO):c.248+7A>G	rs780519881	0.00004
NM_033026.6(PCLO):c.13580G>C (p.Ser4527Thr)	rs377297010	0.00003
NM_033026.6(PCLO):c.5247A>C (p.Lys1749Asn)	rs370974945
NM_033026.6(PCLO):c.6532C>T (p.Pro2178Ser)	rs201432429
NM_033026.6(PCLO):c.9475A>G (p.Ile3159Val)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.