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
31531	MLH1	rs745393750	SNP	missense variant	A/G	326	421	0.42	34	benign	0.033	7001	likely benign	7
31532	MLH1	rs1553651197	SNP	missense variant	R/T	327	591	0.59	1	benign	0	1	likely benign	0
31533	MLH1	rs876659252	SNP	missense variant	Q/L	328	461	0.46	14	benign	0.013	7001	likely benign	7
31534	MLH1	rs989382971	SNP	missense variant	D/N	330	81	0.08	8	benign	0.007	22001	likely benign	22
31535	MLH1	rs1559553545	SNP	missense variant	E/A	331	711	0.71	1	benign	0	19001	likely benign	19
31536	MLH1	rs1553651228	SNP	missense variant	E/Q	332	191	0.19	158	benign	0.157	22001	likely benign	22
31537	MLH1	rs1559553577	SNP	missense variant	M/V	333	331	0.33	1	benign	0	20001	likely benign	20
31538	MLH1	rs1446406061	SNP	missense variant	M/R	333	91	0.09	22	benign	0.021	22001	likely benign	22
31539	MLH1	rs776044212	SNP	missense variant	M/I	333	261	0.26	1	benign	0	22001	likely benign	22
31540	MLH1	rs876659787	SNP	missense variant	L/F	334	711	0.71	1	benign	0	7001	likely benign	7

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