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
17431	MED23	rs753464131	SNP	missense variant	L/V	107	11	0.01	105	benign	0.104	24001	likely benign	24
17432	MED23	rs758795664	SNP	missense variant	T/I	106	31	0.03	73	benign	0.072	16001	likely benign	16
17433	MED23	rs1244889129	SNP	missense variant	D/E	105	1001	1	984	probably damaging	0.983	10001	likely benign	10
17434	MED23	rs112102141	SNP	missense variant	D/G	105	11	0.01	990	probably damaging	0.989	26001	likely benign	26
17435	MED23	rs1480102867	SNP	missense variant	D/N	105	11	0.01	990	probably damaging	0.989	26001	likely benign	26
17436	MED23	rs780331692	SNP	missense variant	I/V	102	11	0.01	769	possibly damaging	0.768	23001	likely benign	23
17437	MED23	rs752075407	SNP	missense variant	S/F	100	751	0.75	384	benign	0.383	22001	likely benign	22
17438	MED23	rs752075407	SNP	missense variant	S/Y	100	1001	1	384	benign	0.383	21001	likely benign	21
17439	MED23	rs755567501	SNP	missense variant	E/V	99	21	0.02	2	benign	0.001	23001	likely benign	23
17440	MED23	rs755567501	SNP	missense variant	E/G	99	1	0	43	benign	0.042	24001	likely benign	24

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