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
1371	PTEN	rs1564566931	SNP	missense variant	P/S	57	11	0.01	1001	probably damaging	1	24001	likely benign	24
1372	PTEN	rs759560822	SNP	missense variant	P/R	57	1	0	1001	probably damaging	1	26001	likely benign	26
1373	PTEN	rs1114167664	substitution	missense variant	G/V	60	1	0	993	probably damaging	0.992	29001	likely benign	29
1374	PTEN	rs1554825226	SNP	missense variant	G/A	60	11	0.01	982	probably damaging	0.981	27001	likely benign	27
1375	PTEN	rs1554825226	SNP	missense variant	G/V	60	1	0	993	probably damaging	0.992	29001	likely benign	29
1376	PTEN	rs121909239	SNP	missense variant	D/G	61	11	0.01	991	probably damaging	0.99	29001	likely benign	29
1377	PTEN	rs121909239	SNP	missense variant	D/V	61	1	0	994	probably damaging	0.993	29001	likely benign	29
1378	PTEN	rs1554825235	SNP	missense variant	I/N	62	1	0	980	probably damaging	0.979	29001	likely benign	29
1379	PTEN	rs1114167633	SNP	missense variant	K/T	63	1	0	1001	probably damaging	1	28001	likely benign	28
1380	PTEN	rs1564566998	SNP	missense variant	V/E	64	1	0	888	possibly damaging	0.887	28001	likely benign	28

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