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
21491	CCREBBP	rs199768244	SNP	missense variant	A/V	254	51	0.05	807	possibly damaging	0.806	22001	likely benign	22
21492	CCREBBP	rs148781922	SNP	missense variant	A/T	254	561	0.56	199	benign	0.198	2001	likely benign	2
21493	CCREBBP	rs142268920	SNP	missense variant	H/L	253	101	0.1	549	possibly damaging	0.548	22001	likely benign	22
21494	CCREBBP	rs1224173039	SNP	missense variant	H/Y	253	41	0.04	921	probably damaging	0.92	23001	likely benign	23
21495	CCREBBP	rs897992674	SNP	missense variant	T/S	251	151	0.15	121	benign	0.12	10001	likely benign	10
21496	CCREBBP	rs1178134399	SNP	missense variant	Q/H	249	31	0.03	984	probably damaging	0.983	22001	likely benign	22
21497	CCREBBP	rs774599450	SNP	missense variant	Q/E	249	11	0.01	792	possibly damaging	0.791	23001	likely benign	23
21498	CCREBBP	rs774599450	SNP	missense variant	Q/K	249	11	0.01	853	possibly damaging	0.852	24001	likely benign	24
21499	CCREBBP	rs374499169	SNP	missense variant	P/L	248	11	0.01	732	possibly damaging	0.731	25001	likely benign	25
21500	CCREBBP	rs761381106	SNP	missense variant	P/S	248	91	0.09	291	benign	0.29	21001	likely benign	21

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