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
4301	MAP3K1	rs766195624	SNP	missense variant	G/V	872	1	0	835	possibly damaging	0.834	23001	likely benign	23
4302	MAP3K1	rs149242419	SNP	missense variant	V/I	873	361	0.36	1	benign	0	1	likely benign	0
4303	MAP3K1	rs149242419	SNP	missense variant	V/L	873	931	0.93	1	benign	0	1	likely benign	0
4304	MAP3K1	rs1196032304	SNP	missense variant	T/A	876	391	0.39	1	benign	0	3001	likely benign	3
4305	MAP3K1	rs755138053	SNP	missense variant	L/S	877	341	0.34	1	benign	0	5001	likely benign	5
4306	MAP3K1	rs778969592	SNP	missense variant	D/G	878	141	0.14	1	benign	0	9001	likely benign	9
4307	MAP3K1	rs748188709	SNP	missense variant	G/D	879	141	0.14	1	benign	0	10001	likely benign	10
4308	MAP3K1	rs778193295	SNP	missense variant	D/G	882	41	0.04	1	benign	0	21001	likely benign	21
4309	MAP3K1	rs747519874	SNP	missense variant	F/Y	884	11	0.01	1	benign	0	22001	likely benign	22
4310	MAP3K1	rs747519874	SNP	missense variant	F/C	884	1	0	294	benign	0.293	22001	likely benign	22

Left 430 431 432