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
28121	ATR	rs765841764	SNP	missense variant	D/E	2298	81	0.08	943	probably damaging	0.942	23001	likely benign	23
28122	ATR	rs1160602567	SNP	missense variant	G/E	2295	31	0.03	744	possibly damaging	0.743	26001	likely benign	26
28123	ATR	rs1356122926	SNP	missense variant	A/V	2294	471	0.47	2	benign	0.001	23001	likely benign	23
28124	ATR	rs370379866	SNP	missense variant	A/S	2294	701	0.7	1	benign	0	14001	likely benign	14
28125	ATR	rs370379866	SNP	missense variant	A/T	2294	391	0.39	22	benign	0.021	17001	likely benign	17
28126	ATR	rs758772379	SNP	missense variant	I/V	2293	11	0.01	80	benign	0.079	22001	likely benign	22
28127	ATR	rs1479311957	SNP	missense variant	A/T	2291	61	0.06	299	benign	0.298	22001	likely benign	22
28128	ATR	rs1180984060	SNP	missense variant	H/R	2289	731	0.73	178	benign	0.177	19001	likely benign	19
28129	ATR	rs1473269172	SNP	missense variant	H/L	2280	441	0.44	1	unknown	0	10001	likely benign	10
28130	ATR	rs747809654	SNP	missense variant	A/V	2278	161	0.16	4	benign	0.003	22001	likely benign	22

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