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
9671	KM2TC-MLL3	rs770827883	SNP	missense variant	E/K	640	121	0.12	1	benign	0	9001	likely benign	9
9672	KM2TC-MLL3	rs769576763	SNP	missense variant	G/V	639	131	0.13	16	benign	0.015	1001	likely benign	1
9673	KM2TC-MLL3	rs769576763	SNP	missense variant	G/D	639	1001	1	1	benign	0	1	likely benign	0
9674	KM2TC-MLL3	rs560300409	SNP	missense variant	G/C	639	31	0.03	316	benign	0.315	14001	likely benign	14
9675	KM2TC-MLL3	rs1193516016	SNP	missense variant	C/F	638	301	0.3	1	benign	0	6001	likely benign	6
9676	KM2TC-MLL3	rs751197859	SNP	missense variant	C/G	638	131	0.13	1	benign	0	4001	likely benign	4
9677	KM2TC-MLL3	rs142435055	SNP	missense variant	I/M	637	51	0.05	56	benign	0.055	2001	likely benign	2
9678	KM2TC-MLL3	rs1470907193	SNP	missense variant	H/Y	636	141	0.14	100	benign	0.099	3001	likely benign	3
9679	KM2TC-MLL3	rs201747335	SNP	missense variant	V/L	634	371	0.37	1	benign	0	6001	likely benign	6
9680	KM2TC-MLL3	rs750509626	SNP	missense variant	S/C	631	171	0.17	1	benign	0	14001	likely benign	14

Left 967 968 969