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
31391	MLH1	rs63750710	SNP	missense variant	H/P	231	211	0.21	804	possibly damaging	0.803	24001	likely benign	24
31392	MLH1	rs878853796	SNP	missense variant	I/V	232	1001	1	7	benign	0.006	3001	likely benign	3
31393	MLH1	rs1559544383	SNP	missense variant	I/T	232	71	0.07	372	benign	0.371	22001	likely benign	22
31394	MLH1	rs550914672	SNP	missense variant	E/K	233	1	0	985	probably damaging	0.984	31001	likely deleterious	31
31395	MLH1	rs1191646988	SNP	missense variant	S/N	234	171	0.17	15	benign	0.014	18001	likely benign	18
31396	MLH1	rs957510193	SNP	missense variant	K/E	235	131	0.13	134	benign	0.133	21001	likely benign	21
31397	MLH1	rs1553648164	SNP	missense variant	K/R	235	201	0.2	47	benign	0.046	20001	likely benign	20
31398	MLH1	rs587781750	SNP	missense variant	G/D	238	11	0.01	597	possibly damaging	0.596	27001	likely benign	27
31399	MLH1	rs587781750	SNP	missense variant	G/A	238	31	0.03	377	benign	0.376	24001	likely benign	24
31400	MLH1	rs763847201	SNP	missense variant	S/C	239	371	0.37	8	benign	0.007	22001	likely benign	22

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