Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
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id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
15191	SPEN	rs1201522610	SNP	missense variant	V/A	3252	541	0.54	1	benign	0	1001	likely benign	1
15192	SPEN	rs746781542	SNP	missense variant	P/S	3253	851	0.85	969	probably damaging	0.968	9001	likely benign	9
15193	SPEN	rs1445646912	SNP	missense variant	V/L	3254	311	0.31	4	benign	0.003	2001	likely benign	2
15194	SPEN	rs1251041671	SNP	missense variant	V/A	3254	91	0.09	12	benign	0.011	2001	likely benign	2
15195	SPEN	rs200093315	SNP	missense variant	P/A	3257	301	0.3	578	possibly damaging	0.577	8001	likely benign	8
15196	SPEN	rs200093315	SNP	missense variant	P/S	3257	731	0.73	745	possibly damaging	0.744	8001	likely benign	8
15197	SPEN	rs551660149	SNP	missense variant	P/S	3259	121	0.12	677	possibly damaging	0.676	9001	likely benign	9
15198	SPEN	rs1173078727	SNP	missense variant	A/P	3260	221	0.22	2	benign	0.001	8001	likely benign	8
15199	SPEN	rs1162270194	SNP	missense variant	P/L	3261	1	0	779	possibly damaging	0.778	22001	likely benign	22
15200	SPEN	rs1369676611	SNP	missense variant	G/S	3265	1001	1	6	benign	0.005	1	likely benign	0

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