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Table 2 Overview of results for 4820 variants, of which 62 variants had been classified as pathogenic or likely pathogenic in APC, ATM, BRCA1, BRCA2, CDKN2A, MEN1 and PTEN

From: Development and validation of next generation sequencing based 35-gene hereditary cancer panel

GeneTotal VariantsTrue PositivesFalse PositivesFalse Negatives
APC62262200
ATM17617600
BAP1171700
BARD129829800
BMPR1A828200
BRCA139939900
BRCA257757700
BRIP133133100
CDH111611600
CDK40000
CDKN2A292900
CHEK2191900
EPCAM11111100
GREM1313100
MEN125225200
MITF4400
MLH1343400
MRE1114014000
MSH210410400
MSH610410400
MUTYH767600
NBN26026000
PALB2414100
PMS1101000
PMS236236206a
POLD112412400
POLE32232200
PTEN7700
RAD50101000
RAD51C101000
RAD51D555500
SMAD40000
STK118800
TP53858500
XRCC24400
TOTAL4820482006a
  1. a6 variants at the position Chr7:6013153 in PMS2 is a false negative. But, this is in a pseudogene region and is also a benign variant