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
7361	KM2TC-MLL3	rs764685940	SNP	missense variant	Q/E	3675	161	0.16	1	benign	0	17001	likely benign	17
7362	KM2TC-MLL3	rs752291776	SNP	missense variant	G/D	3674	41	0.04	256	benign	0.255	13001	likely benign	13
7363	KM2TC-MLL3	rs1320038786	SNP	missense variant	G/C	3674	1	0	820	possibly damaging	0.819	19001	likely benign	19
7364	KM2TC-MLL3	rs1225519033	SNP	missense variant	A/G	3673	261	0.26	55	benign	0.054	7001	likely benign	7
7365	KM2TC-MLL3	rs1483692784	SNP	missense variant	A/V	3672	181	0.18	1	benign	0	8001	likely benign	8
7366	KM2TC-MLL3	rs1167402234	SNP	missense variant	A/T	3672	231	0.23	2	benign	0.001	7001	likely benign	7
7367	KM2TC-MLL3	rs1300600766	SNP	missense variant	M/I	3671	411	0.41	4	benign	0.003	1	likely benign	0
7368	KM2TC-MLL3	rs879219321	SNP	missense variant	N/S	3670	1001	1	2	benign	0.001	1	likely benign	0
7369	KM2TC-MLL3	rs751536561	SNP	missense variant	P/L	3666	141	0.14	24	benign	0.023	13001	likely benign	13
7370	KM2TC-MLL3	rs751536561	SNP	missense variant	P/R	3666	11	0.01	16	benign	0.015	16001	likely benign	16

Left 736 737 738