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
11011	MLLT4	rs893146467	SNP	missense variant	G/D	90	71	0.07	1000	probably damaging	0.999	23001	likely benign	23
11012	MLLT4	rs1455784406	SNP	missense variant	S/A	91	211	0.21	131	benign	0.13	16001	likely benign	16
11013	MLLT4	rs1157380705	SNP	missense variant	S/F	91	151	0.15	838	possibly damaging	0.837	24001	likely benign	24
11014	MLLT4	rs781351095	SNP	missense variant	T/P	92	141	0.14	6	benign	0.005	9001	likely benign	9
11015	MLLT4	rs781351095	SNP	missense variant	T/A	92	771	0.77	1	benign	0	1001	likely benign	1
11016	MLLT4	rs1396620473	SNP	missense variant	T/S	92	1001	1	1	benign	0	7001	likely benign	7
11017	MLLT4	rs148307373	SNP	missense variant	P/A	94	81	0.08	998	probably damaging	0.997	22001	likely benign	22
11018	MLLT4	rs762626146	SNP	missense variant	P/H	94	1	0	1000	probably damaging	0.999	23001	likely benign	23
11019	MLLT4	rs200779172	SNP	missense variant	P/L	95	141	0.14	1000	probably damaging	0.999	23001	likely benign	23
11020	MLLT4	rs1334582106	SNP	missense variant	E/G	96	1	0	319	benign	0.318	27001	likely benign	27

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