Basal Cell Neoplasm — Genomics

Basal Cell Neoplasm — Genomics · CancerIndex

Genomics

Gene alteration frequencies by cohort

1 cohort mapped to this entity or its descendants. Each frequency is affected / profiled within one cohort; cohorts are shown separately because case selection, sequencing depth and definitions differ. By default the cohort with the most cases profiled is shown.

Basal Cell Carcinoma (UNIGE, Nat Genet 2016) bcc_unige_2016UNIGE

293 cases with simple somatic mutation data · 293 cases total · 2026-01-05 · mapped to Skin Basal Cell Carcinoma EXACT_IDENTIFIER

cbioportalObserved30 genes · frequency = affected / profiled, as published by the cohort.

#	Gene	Alteration	Affected (n)	Profiled (n)	Frequency (%)	Source
16	TTN	Ssm	112	126	88.9%	cbioportal
21	MUC16	Ssm	103	126	81.7%	cbioportal
1	PTCH1	Ssm	221	293	75.4%	cbioportal
2	CSMD3	Ssm	212	293	72.4%	cbioportal
3	CSMD1	Ssm	203	293	69.3%	cbioportal
4	LRP1B	Ssm	197	293	67.2%	cbioportal
32	ADGRV1	Ssm	82	126	65.1%	cbioportal
36	SYNE1

Data updated 22 days agoSource updated 2026-01-05

Cohorts mapped to a descendant (e.g. a subtype) are included because their cases belong to this entity by definition; the mapping and its match type are shown per cohort.