chr7:55242454:> Detail (hg19) (EGFR)

Information

Genome

Assembly Position
hg19 chr7:55,242,454-55,242,456
hg38 chr7:55,174,761-55,174,763 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
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 D Predictive Supports Sensitivity/Response Somatic 19147750 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
In an in vitro study, a Ba/F3 cell line expressing EGFR V742A demonstrated increased sensitivity to ... 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
hg19
Position
chr7:55,242,454-55,242,456
Variant Type
snv
Variant (CIViC) (CIViC Variant)
V742A
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/1001
Genome browser