chr8:31640426:> Detail (hg38) (NRG1)

Information

Genome

Assembly Position
hg19 chr8:31,497,942-32,622,294 
hg38 chr8:31,640,426-32,764,776

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
head and neck squamous cell carcinoma Lapatinib D Predictive Supports Sensitivity/Response N/A 4 21840482 Detail
colorectal cancer Cetuximab D Predictive Supports Resistance N/A 4 21900593 Detail
ovarian cancer Seribantumab D Predictive Supports Sensitivity/Response N/A 3 20227043 Detail
lung non-small cell carcinoma Cisplatin,Gemcitabine,Carboplatin,Paclitaxel D Predictive Supports Sensitivity/Response N/A 3 23390248 Detail
lung non-small cell carcinoma Patritumab B Predictive Supports Sensitivity/Response Somatic 4 26137564 Detail
cancer Anti-ErbB3 Monoclonal Antibody AV-203 D Predictive Supports Sensitivity/Response N/A 3 25542901 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
In non-HER2 amplified cell lines, sensitivity to HER2 kinase inhibitor lapatinib was found mainly in... CIViC Evidence Detail
NRG1 upregulation or ERBB2 amplification were the main causes of resistance to cetuximab in-vivo and... CIViC Evidence Detail
An NRG1-ERBB3 autocrine signal-transducing loop was identified in a subset of ovarian cancers and ce... CIViC Evidence Detail
In-vivo studies of residual NSCLC tumors (xenografts of 5 cell lines) after chemotherapy found incre... CIViC Evidence Detail
In this phase-2 study, 215 patients were randomized to either erlotinib and placebo or erlotinib and... CIViC Evidence Detail
This screening study in various tumor xenografts identified NRG1 expression to correlate with sensiv... 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
chr8:31,640,426-32,764,776
Variant Type
snv
Variant (CIViC) (CIViC Variant)
EXPRESSION
Transcript 1 (CIViC Variant)
ENST00000523534.1
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/314
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