TP53, tumor protein p53, 7157

N. diseases: 2494; N. variants: 527
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.100 0.966 29 2003 2018
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.100 0.966 29 2003 2018
dbSNP: rs1131691021
rs1131691021
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.060 0.833 6 2010 2019
dbSNP: rs28934575
rs28934575
0.641 0.400 17 7674230 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.740 1.000 6 2006 2018
dbSNP: rs28934571
rs28934571
0.645 0.360 17 7674216 missense variant C/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.050 1.000 5 2001 2013
dbSNP: rs879253942
rs879253942
0.677 0.400 17 7673826 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.040 1.000 4 2008 2019
dbSNP: rs1057519975
rs1057519975
0.649 0.480 17 7675209 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2007 2019
dbSNP: rs1057519992
rs1057519992
0.742 0.400 17 7674890 missense variant T/A;C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 1991 2008
dbSNP: rs1064795841
rs1064795841
0.882 0.080 17 7674971 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2013 2015
dbSNP: rs587780073
rs587780073
0.708 0.400 17 7674262 missense variant T/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2008 2019
dbSNP: rs730882002
rs730882002
0.925 0.040 17 7674956 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2017 2017
dbSNP: rs78378222
rs78378222
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2015 2019
dbSNP: rs1057519747
rs1057519747
0.716 0.280 17 7675094 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs1057519976
rs1057519976
17 7675207 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1057520001
rs1057520001
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 1995 1995
dbSNP: rs1060501201
rs1060501201
0.925 0.080 17 7674190 missense variant T/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1064793929
rs1064793929
0.882 0.280 17 7675167 frameshift variant A/-;AA delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs112431538
rs112431538
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1131691036
rs1131691036
0.851 0.080 17 7675207 frameshift variant GCA/CC delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1555526711
rs1555526711
17 7676171 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2002 2002
dbSNP: rs193920774
rs193920774
0.695 0.440 17 7673823 missense variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs193920817
rs193920817
0.925 0.160 17 7675131 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs267605077
rs267605077
0.925 0.080 17 7675212 missense variant A/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 < 0.001 1 2009 2009
dbSNP: rs397516434
rs397516434
1.000 0.120 17 7670669 missense variant G/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2006 2006