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
13861	SPEN	rs772866760	SNP	missense variant	Y/C	1399	81	0.08	1	benign	0	19001	likely benign	19
13862	SPEN	rs1213107603	SNP	missense variant	S/G	1401	211	0.21	2	benign	0.001	19001	likely benign	19
13863	SPEN	rs746483518	SNP	missense variant	S/N	1401	231	0.23	2	benign	0.001	16001	likely benign	16
13864	SPEN	rs1308286819	SNP	missense variant	R/Q	1403	21	0.02	989	probably damaging	0.988	25001	likely benign	25
13865	SPEN	rs770382670	SNP	missense variant	L/S	1404	1	0	726	possibly damaging	0.725	25001	likely benign	25
13866	SPEN	rs770382670	SNP	missense variant	L/W	1404	1	0	889	possibly damaging	0.888	25001	likely benign	25
13867	SPEN	rs776034493	SNP	missense variant	R/G	1409	41	0.04	995	probably damaging	0.994	27001	likely benign	27
13868	SPEN	rs763419267	SNP	missense variant	D/H	1413	61	0.06	16	benign	0.015	22001	likely benign	22
13869	SPEN	rs1463541590	SNP	missense variant	L/V	1415	91	0.09	16	benign	0.015	8001	likely benign	8
13870	SPEN	rs762271842	SNP	missense variant	R/C	1416	1	0	995	probably damaging	0.994	27001	likely benign	27

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