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
28031	ATR	rs762196224	SNP	missense variant	A/V	2575	71	0.07	305	benign	0.304	23001	likely benign	23
28032	ATR	rs1206972227	SNP	missense variant	H/R	2559	1	0	986	probably damaging	0.985	26001	likely benign	26
28033	ATR	rs200490116	SNP	missense variant	T/S	2556	171	0.17	587	possibly damaging	0.586	23001	likely benign	23
28034	ATR	rs1043401586	SNP	missense variant	V/D	2553	1	0	1001	probably damaging	1	28001	likely benign	28
28035	ATR	rs768497377	SNP	missense variant	M/V	2551	11	0.01	881	possibly damaging	0.88	23001	likely benign	23
28036	ATR	rs1210518431	SNP	missense variant	R/L	2547	31	0.03	757	possibly damaging	0.756	29001	likely benign	29
28037	ATR	rs769121210	SNP	missense variant	R/H	2544	1	0	1001	probably damaging	1	26001	likely benign	26
28038	ATR	rs1193437141	SNP	missense variant	R/C	2544	61	0.06	1001	probably damaging	1	23001	likely benign	23
28039	ATR	rs915275959	SNP	missense variant	M/I	2540	81	0.08	11	benign	0.01	20001	likely benign	20
28040	ATR	rs763127779	SNP	missense variant	R/Q	2533	1	0	1001	probably damaging	1	31001	likely deleterious	31

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