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
9391	KM2TC-MLL3	rs1393613102	SNP	missense variant	S/N	881	1	0	880	possibly damaging	0.879	24001	likely benign	24
9392	KM2TC-MLL3	rs1440820446	SNP	missense variant	I/T	879	121	0.12	237	benign	0.236	22001	likely benign	22
9393	KM2TC-MLL3	rs751727499	SNP	missense variant	A/V	878	71	0.07	195	benign	0.194	23001	likely benign	23
9394	KM2TC-MLL3	rs757340270	SNP	missense variant	S/I	877	1	0	439	benign	0.438	23001	likely benign	23
9395	KM2TC-MLL3	rs757340270	SNP	missense variant	S/T	877	71	0.07	396	benign	0.395	20001	likely benign	20
9396	KM2TC-MLL3	rs1417990221	SNP	missense variant	G/S	876	121	0.12	977	probably damaging	0.976	24001	likely benign	24
9397	KM2TC-MLL3	rs781062747	SNP	missense variant	Q/L	873	11	0.01	618	possibly damaging	0.617	25001	likely benign	25
9398	KM2TC-MLL3	rs781062747	SNP	missense variant	Q/R	873	141	0.14	691	possibly damaging	0.69	23001	likely benign	23
9399	KM2TC-MLL3	rs746453043	SNP	missense variant	R/W	872	1	0	1000	probably damaging	0.999	26001	likely benign	26
9400	KM2TC-MLL3	rs746453043	SNP	missense variant	R/G	872	1	0	995	probably damaging	0.994	25001	likely benign	25

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