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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006031.6(PCNT):c.2575G>A (p.Asp859Asn)	rs115369710	0.00703
NM_006031.6(PCNT):c.8646G>C (p.Leu2882Phe)	rs141771795	0.00596
NM_006031.6(PCNT):c.5954C>T (p.Ser1985Phe)	rs140398533	0.00585
NM_006031.6(PCNT):c.6933C>T (p.Val2311=)	rs148444313	0.00289
NM_006031.6(PCNT):c.6957T>G (p.Phe2319Leu)	rs61735813	0.00115
NM_006031.6(PCNT):c.979G>C (p.Glu327Gln)	rs575720246	0.00045
NM_006031.6(PCNT):c.7118G>A (p.Gly2373Glu)	rs147670568	0.00032
NM_006031.6(PCNT):c.7459C>G (p.Leu2487Val)	rs201185279	0.00014
NM_006031.6(PCNT):c.6141C>T (p.Asp2047=)	rs144445891	0.00005
NM_006031.6(PCNT):c.2108A>T (p.Tyr703Phe)	rs572444748
NM_006031.6(PCNT):c.5994+13dup	rs772752236
NM_006031.6(PCNT):c.8830_8832del (p.Lys2944del)	rs562568796
NM_006031.6(PCNT):c.8889G>A (p.Ser2963=)	rs151325202

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