Source: CLINVAR

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: rs28937578
rs28937578
EP300 ; EP300-AS1
1.000 0.080 22 41178373 missense variant C/A;T snv 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 0
dbSNP: rs1555905780
rs1555905780
EP300
22 41117361 frameshift variant C/- delins
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.700 1.000 19 1963 2016
dbSNP: rs1555907278
rs1555907278
EP300
22 41127646 stop gained C/T snv
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.700 1.000 19 1963 2016
dbSNP: rs1555907749
rs1555907749
EP300
22 41131612 frameshift variant -/T delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.700 1.000 19 1963 2016
dbSNP: rs1555911098
rs1555911098
EP300
22 41168719 splice acceptor variant A/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.700 1.000 19 1963 2016
dbSNP: rs1555911313
rs1555911313
EP300
1.000 22 41170482 stop gained C/T snv
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.700 1.000 19 1963 2016
dbSNP: rs1555911313
rs1555911313
EP300
1.000 22 41170482 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.700 1.000 19 1963 2016
dbSNP: rs886037664
rs886037664
EP300
1.000 0.120 22 41117194 frameshift variant CTCT/- delins
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 2 2014 2016
dbSNP: rs1057519375
rs1057519375
EP300 ; EP300-AS1
1.000 0.120 22 41178931 frameshift variant CA/- delins
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.700 1.000 1 2016 2016
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		0.700 1.000 1 2016 2016
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519889
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs1114167305
rs1114167305
EP300
1.000 0.120 22 41162784 splice region variant G/C snv
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015
dbSNP: rs1114167306
rs1114167306
EP300
1.000 0.120 22 41172557 missense variant T/G snv
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015
dbSNP: rs1210404526
rs1210404526
EP300 ; EP300-AS1
0.925 0.120 22 41177712 missense variant C/G;T snv 4.0E-06
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		0.700 1.000 1 2018 2018
dbSNP: rs1210404526
rs1210404526
EP300 ; EP300-AS1
0.925 0.120 22 41177712 missense variant C/G;T snv 4.0E-06
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2018 2018
dbSNP: rs139310551
rs139310551
EP300 ; EP300-AS1
1.000 0.120 22 41176400 stop gained C/A;T snv
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015
dbSNP: rs1555912040
rs1555912040
EP300 ; EP300-AS1
1.000 0.120 22 41176420 frameshift variant -/ATGT delins
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015
dbSNP: rs1569118537
rs1569118537
EP300
0.925 0.200 22 41172631 stop gained C/T snv
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2016 2016
dbSNP: rs1569118537
rs1569118537
EP300
0.925 0.200 22 41172631 stop gained C/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs565779970
rs565779970
EP300
0.925 0.120 22 41158483 stop gained T/A;C snv 3.2E-05
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2005 2005
dbSNP: rs587778256
rs587778256
EP300 ; EP300-AS1
1.000 0.120 22 41178337 inframe deletion CCAGTTCCAGCA/- delins 1.6E-03 1.7E-03
CUI: C3150941
Disease: RUBINSTEIN-TAYBI SYNDROME 2
RUBINSTEIN-TAYBI SYNDROME 2 		0.700 1.000 1 2015 2015