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
2611	ZNF703	rs951099652	SNP	missense variant	G/S	446	1	0	968	probably damaging	0.967	32001	likely deleterious	32
2612	ZNF703	rs1410534350	SNP	missense variant	F/L	447	11	0.01	113	benign	0.112	23001	likely benign	23
2613	ZNF703	rs540084351	SNP	missense variant	M/T	448	1	0	265	benign	0.264	24001	likely benign	24
2614	ZNF703	rs928433112	SNP	missense variant	N/K	451	1	0	891	possibly damaging	0.89	24001	likely benign	24
2615	ZNF703	rs762668585	SNP	missense variant	E/V	452	1	0	638	possibly damaging	0.637	31001	likely deleterious	31
2616	ZNF703	rs1424414620	SNP	missense variant	P/T	453	31	0.03	27	benign	0.026	23001	likely benign	23
2617	ZNF703	rs1301837169	SNP	missense variant	P/R	453	1	0	831	possibly damaging	0.83	27001	likely benign	27
2618	ZNF703	rs1301837169	SNP	missense variant	P/L	453	1	0	300	benign	0.299	24001	likely benign	24
2619	ZNF703	rs1436614646	SNP	missense variant	P/L	455	1	0	778	possibly damaging	0.777	26001	likely benign	26
2620	ZNF703	rs759480984	SNP	missense variant	S/G	457	11	0.01	31	benign	0.03	24001	likely benign	24

Left 261 262 263