FGFR2 c.1722+11_1722+12insA Detail (hg19) (FGFR2)

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

Genome

Assembly	Position
hg19	chr10:123,247,493-123,247,493
hg38	chr10:121,487,979-121,487,979

HGVS

FGFR2

Type	Transcript	Protein
RefSeq	NM_001144919.1:c.1722+11_1722+12insA
	NM_001320654.1:c.1302+11_1302+12insA
	NM_001144916.1:c.1635+11_1635+12insA
	NM_001144918.1:c.1635+11_1635+12insA
	NM_001144917.1:c.1638+11_1638+12insA
	NM_000141.4:c.1986+11_1986+12insA
	NM_001144915.1:c.1719+11_1719+12insA
	NM_001144914.1:c.1650+11_1650+12insA
	NM_001144913.1:c.1989+11_1989+12insA
	NM_022970.3:c.1989+11_1989+12insA
	NM_001320658.1:c.1719+11_1719+12insA
	NM_023029.2:c.1719+11_1719+12insA
Ensemble	ENST00000360144.7:c.1722+11_1722+12insA
	ENST00000478859.5:c.1302+11_1302+12insA
	ENST00000356226.8:c.1635+11_1635+12insA
	ENST00000369060.8:c.1638+11_1638+12insA
	ENST00000358487.10:c.1986+11_1986+12insA
	ENST00000357555.9:c.1719+11_1719+12insA
	ENST00000369061.8:c.1650+11_1650+12insA
	ENST00000369056.5:c.1989+11_1989+12insA
	ENST00000457416.7:c.1989+11_1989+12insA
	ENST00000351936.11:c.1980+11_1980+12insA
	ENST00000369059.5:c.1644+11_1644+12insA
	ENST00000346997.6:c.1980+11_1980+12insA
	ENST00000613048.4:c.1719+11_1719+12insA
	ENST00000638709.2:c.810+11_810+12insA
	ENST00000682550.1:c.1635+11_1635+12insA
	ENST00000682772.1:c.810+11_810+12insA
	ENST00000683211.1:c.1980+11_1980+12insA
	ENST00000684153.1:c.1635+11_1635+12insA

Summary

MGeND

Clinical significance	not provided
Variant entry	2
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

Links

FGFR2

Type	Database	ID	Link
Gene	MIM	176943	OMIM
	HGNC	3689	HGNC
	Ensembl	ENSG00000066468	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
not provided		ileum	not provided	MGS000041 (TMGS000094)	Hitoshi Nakagama	National Cancer Center Japan
not provided		bronchus or lung, unspecified	not provided	MGS000041 (TMGS000094)	Hitoshi Nakagama	National Cancer Center Japan

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

[No Data.]

Annotation

OVERLAPPED TRANSCRIPT
INFO

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
Genome: hg19
Position: chr10:123,247,493-123,247,493
Variant Type: snv
Reference Allele: -
Alternative Allele: T

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