chr7:55019101:> Detail (hg38) (EGFR)

Information

Genome

Assembly Position
hg19 chr7:55,086,794-55,279,321 
hg38 chr7:55,019,101-55,211,628

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
colorectal cancer Cetuximab B Predictive Supports Sensitivity/Response N/A 4 18003960 Detail
colorectal cancer Panitumumab B Predictive Supports Sensitivity/Response N/A 2 17470858 Detail
colorectal cancer Cetuximab B Predictive Supports Sensitivity/Response N/A 1 14993230 Detail
chordoma Lapatinib B Predictive Supports Sensitivity/Response N/A 3 23559153 Detail
lung non-small cell carcinoma Gefitinib B Predictive Supports Sensitivity/Response 3 12748244 Detail
head and neck squamous cell carcinoma Docetaxel,Cetuximab B Predictive Does Not Support Sensitivity/Response Somatic 3 21653686 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Patients with refractory colorectal cancer expressing immunohistochemically detectable EGFR were ran... CIViC Evidence Detail
463 patients with 1% or more EGFR tumor cell membrane staining, with metastatic CRC progressive afte... CIViC Evidence Detail
57 patients with chemorefractory colorectal cancer expressing EGFR (IHC staining) were treated with ... CIViC Evidence Detail
18 advanced progressing chordoma patients entered this study (median age: 61 years; disease extent: ... CIViC Evidence Detail
Double blind Phase II clinical trial found an objective response rate of 18.4% and 19% for two group... CIViC Evidence Detail
47 HNSCC patients treated with cetuximab/docetaxel were retrospectively analyzed for EGFRvIII, EGFR ... 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
chr7:55,019,101-55,211,628
Variant Type
snv
Variant (CIViC) (CIViC Variant)
EXPRESSION
Transcript 1 (CIViC Variant)
ENST00000275493.2
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/354
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