Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
10341	ARID1B	rs1191841397	SNP	missense variant	P/A	221	131	0.13	69	benign	0.068	11001	likely benign	11
10342	ARID1B	rs1191841397	SNP	missense variant	P/S	221	881	0.88	142	benign	0.141	8001	likely benign	8
10343	ARID1B	rs1252378435	SNP	missense variant	P/L	221	31	0.03	740	possibly damaging	0.739	22001	likely benign	22
10344	ARID1B	rs777266582	SNP	missense variant	V/L	224	11	0.01	970	probably damaging	0.969	20001	likely benign	20
10345	ARID1B	rs777266582	SNP	missense variant	V/F	224	1	0	998	probably damaging	0.997	23001	likely benign	23
10346	ARID1B	rs1554247605	substitution	missense variant	V/P	224	1	0	647	possibly damaging	0.646		-
10347	ARID1B	rs746730857	SNP	missense variant	V/A	224	301	0.3	945	probably damaging	0.944	19001	likely benign	19
10348	ARID1B	rs770339919	SNP	missense variant	P/T	225	491	0.49	732	possibly damaging	0.731	13001	likely benign	13
10349	ARID1B	rs1439723202	SNP	missense variant	P/R	225	81	0.08	964	probably damaging	0.963	22001	likely benign	22
10350	ARID1B	rs1209412991	SNP	missense variant	Y/H	230	1	0	1000	probably damaging	0.999	22001	likely benign	22

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