Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1554292741
rs1554292741
7 5973454 missense variant T/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2013 2016
dbSNP: rs886039646
rs886039646
1.000 0.160 7 5973467 frameshift variant A/- del 2.8E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs786201039
rs786201039
7 5973482 stop gained C/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2013 2013
dbSNP: rs587781626
rs587781626
1.000 0.160 7 5973487 frameshift variant AT/C delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs774583397
rs774583397
7 5973543 splice acceptor variant C/A;G snv 8.7E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs876661113
rs876661113
7 5977587 splice donor variant C/A;G;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 2009 2015
dbSNP: rs587779338
rs587779338
0.851 0.200 7 5977589 missense variant G/A snv 1.0E-05 2.1E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 10 2010 2018
dbSNP: rs1554293810
rs1554293810
7 5977620 stop gained G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs63751466
rs63751466
0.882 0.200 7 5977629 stop gained G/A;T snv 2.7E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2011 2016
dbSNP: rs1231406078
rs1231406078
7 5977650 frameshift variant -/A delins 7.1E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2010 2010
dbSNP: rs267608160
rs267608160
0.925 0.200 7 5977669 frameshift variant GAAG/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2000 2011
dbSNP: rs1554293991
rs1554293991
7 5977737 stop gained T/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs1554294393
rs1554294393
7 5978595 splice donor variant C/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs587779337
rs587779337
1.000 0.160 7 5978622 missense variant C/A;T snv 8.0E-06; 4.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 8 2008 2017
dbSNP: rs267608173
rs267608173
0.925 0.160 7 5978625 frameshift variant TTCT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2005 2006
dbSNP: rs63750695
rs63750695
0.851 0.280 7 5978675 frameshift variant AAGTT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2004 2008
dbSNP: rs1060503110
rs1060503110
7 5978679 stop gained A/C;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2015 2015
dbSNP: rs1554294508
rs1554294508
7 5978687 frameshift variant AGT/C delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs267608172
rs267608172
0.925 0.160 7 5982823 splice donor variant C/A;G;T snv 4.1E-06; 1.6E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 2008 2016
dbSNP: rs786201062
rs786201062
7 5982842 frameshift variant T/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2014 2014
dbSNP: rs876659480
rs876659480
7 5982843 stop gained G/A snv 8.5E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2015 2015
dbSNP: rs876659900
rs876659900
0.925 0.120 7 5982861 stop gained G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs587782704
rs587782704
0.925 0.160 7 5982881 frameshift variant T/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2016 2016
dbSNP: rs267608161
rs267608161
0.851 0.200 7 5982885 missense variant C/T snv 4.0E-05 2.8E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 8 1997 2017
dbSNP: rs587781317
rs587781317
7 5982903 missense variant C/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2010 2013