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: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.100 0.833 12 2006 2019
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.100 0.900 10 2006 2017
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.100 0.900 10 2006 2017
dbSNP: rs563378859
rs563378859
0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.030 1.000 3 2008 2016
dbSNP: rs121912654
rs121912654
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.020 1.000 2 2013 2016
dbSNP: rs28934578
rs28934578
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.020 1.000 2 2010 2011
dbSNP: rs762846821
rs762846821
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.020 1.000 2 2009 2016
dbSNP: rs770374782
rs770374782
0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.020 1.000 2 2010 2018
dbSNP: rs121913343
rs121913343
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs137852789
rs137852789
0.925 0.080 17 7675152 missense variant C/G;T snv 4.0E-06 3.5E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1453167097
rs1453167097
0.925 0.080 17 7675172 missense variant A/C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs749817236
rs749817236
1.000 0.040 17 7669624 frameshift variant C/- delins
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs78378222
rs78378222
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2013 2013