chr7:55191725:A>T Detail (hg38) (EGFR)

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

Genome

Assembly	Position
hg19	chr7:55,259,418-55,259,418 View the variant detail on this assembly version.
hg38	chr7:55,191,725-55,191,725

HGVS

EGFR

Type	Transcript	Protein
RefSeq	NM_005228.3:c.2476A>T	NP_005219.2:p.Asn826Tyr
	NM_001346897.1:c.2341A>T	NP_001333826.1:p.Asn781Tyr
Ensemble	ENST00000275493.7:c.2476A>T	ENST00000275493.7:p.Asn826Tyr
	ENST00000450046.2:c.2317A>T	ENST00000450046.2:p.Asn773Tyr
	ENST00000455089.5:c.2341A>T	ENST00000455089.5:p.Asn781Tyr

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

Links

EGFR

Type	Database	ID	Link
Gene	MIM	131550	OMIM
	HGNC	3236	HGNC
	Ensembl	ENSG00000146648	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
lung non-small cell carcinoma	Erlotinib	C	Predictive	Does Not Support	Sensitivity/Response	Somatic	2	21531810	Detail

DisGeNET

[No Data.]

Annotation

Annotations

Descrption	Source	Links
In a study, 1 participant with stage IV lung adenocarcinoma was sequenced at EGFR exons 18 to 21 and...	CIViC Evidence	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
Genome: hg38
Position: chr7:55,191,725-55,191,725
Variant Type: snv
Reference Allele: A
Alternative Allele: T
Variant (CIViC) (CIViC Variant): N826Y
Transcript 1 (CIViC Variant): ENST00000275493.2
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/1896

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