BRAF WASFL-BRAF Fusion Detail (hg38) (BRAF)

Go to:

Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
Genome browser

Information

Genome

Assembly	Position
hg19	chr7:140,419,127-140,624,729 View the variant detail on this assembly version.

hg38	chr7:140,719,327-140,924,929

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

Links

Type	Database	ID	Link
Gene	MIM	164757	OMIM
	HGNC	1097	HGNC
	Ensembl	ENSG00000157764	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

Disease	Drug	EL	ET	ED	CS	VO	TR	Pubmed	Links
cancer	Vemurafenib	C	Predictive	Does Not Support	Sensitivity/Response	Somatic	2	29320312	Detail

DisGeNET

[No Data.]

Annotation

ANNOTATION
INFO

Annotations

Descrption	Source	Links
The phase 2a MyPathway study assigned patients with HER2, EGFR, BRAF or SHH alterations to treatment...	CIViC Evidence	Detail

Gene: BRAF
Genome: hg38
Position: chr7:140,719,327-140,924,929
Variant Type: fusion
Variant (CIViC) (CIViC Variant): WASFL-BRAF Fusion
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/2228
Variant (CIViC) (CIViC Variant): FAM73A-BRAF fusion
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/2987

Genome browser