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
1691	ERBB2	rs756588194	SNP	missense variant	E/D	332	161	0.16	25	benign	0.024	19001	likely benign	19
1692	ERBB2	rs1409114304	SNP	missense variant	C/Y	334	1	0	1001	probably damaging	1	27001	likely benign	27
1693	ERBB2	rs1409114304	SNP	missense variant	C/F	334	1	0	1001	probably damaging	1	27001	likely benign	27
1694	ERBB2	rs532077147	SNP	missense variant	R/Q	340	21	0.02	4	benign	0.003	22001	likely benign	22
1695	ERBB2	rs747993530	SNP	missense variant	Y/C	343	31	0.03	975	probably damaging	0.974	29001	likely benign	29
1696	ERBB2	rs758204762	SNP	missense variant	G/S	344	31	0.03	984	probably damaging	0.983	29001	likely benign	29
1697	ERBB2	rs758204762	SNP	missense variant	G/R	344	1	0	1000	probably damaging	0.999	28001	likely benign	28
1698	ERBB2	rs1037129509	SNP	missense variant	G/D	344	11	0.01	1000	probably damaging	0.999	28001	likely benign	28
1699	ERBB2	rs1460443371	SNP	missense variant	G/S	346	11	0.01	755	possibly damaging	0.754	28001	likely benign	28
1700	ERBB2	rs746686273	SNP	missense variant	M/K	347	81	0.08	16	benign	0.015	22001	likely benign	22

Left 169 170 171