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
29431	ERBB3	rs1057519893	SNP	missense variant	V/L	104	41	0.04	120	benign	0.119	22001	likely benign	22
29432	ERBB3	rs984896	SNP	missense variant	V/G	105	1	0	888	possibly damaging	0.887	26001	likely benign	26
29433	ERBB3	rs780976894	SNP	missense variant	R/Q	106	1	0	1000	probably damaging	0.999	29001	likely benign	29
29434	ERBB3	rs780976894	SNP	missense variant	R/L	106	1	0	1000	probably damaging	0.999	31001	likely deleterious	31
29435	ERBB3	rs1418372214	SNP	missense variant	G/E	107	1	0	1001	probably damaging	1	27001	likely benign	27
29436	ERBB3	rs1476037377	SNP	missense variant	T/A	108	81	0.08	1	benign	0	22001	likely benign	22
29437	ERBB3	rs1313980887	SNP	missense variant	Q/H	109	121	0.12	16	benign	0.015	19001	likely benign	19
29438	ERBB3	rs1162297781	SNP	missense variant	V/I	110	11	0.01	24	benign	0.023	22001	likely benign	22
29439	ERBB3	rs1462065910	SNP	missense variant	D/N	112	1	0	20	benign	0.019	24001	likely benign	24
29440	ERBB3	rs769723853	SNP	missense variant	D/G	112	1	0	8	benign	0.007	24001	likely benign	24

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