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
31221	MLH1	rs762099920	SNP	missense variant	R/P	119	11	0.01	1000	probably damaging	0.999	31001	likely deleterious	31
31222	MLH1	rs750650349	SNP	missense variant	S/P	120	251	0.25	612	possibly damaging	0.611	24001	likely benign	24
31223	MLH1	rs1799977	SNP	missense variant	I/L	121	381	0.38	101	benign	0.1	21001	likely benign	21
31224	MLH1	rs1799977	SNP	missense variant	I/V	121	371	0.37	29	benign	0.028	17001	likely benign	17
31225	MLH1	rs1799977	SNP	missense variant	I/F	121	1	0	937	probably damaging	0.936	24001	likely benign	24
31226	MLH1	rs1553644227	SNP	missense variant	I/T	121	1	0	877	possibly damaging	0.876	25001	likely benign	25
31227	MLH1	rs1553644231	SNP	missense variant	I/M	121	1	0	952	probably damaging	0.951	23001	likely benign	23
31228	MLH1	rs766517126	SNP	missense variant	N/S	124	491	0.49	15	benign	0.014	17001	likely benign	17
31229	MLH1	rs751719069	SNP	missense variant	N/K	124	141	0.14	102	benign	0.101	20001	likely benign	20
31230	MLH1	rs756045117	SNP	missense variant	A/G	125	31	0.03	193	benign	0.192	23001	likely benign	23

Left 3122 3123 3124