Overview

Gene Location [1]
17q12
Pathway
Receptor tyrosine kinase/growth factor signaling
Variant Type
Substitution - Missense
Affected Exon Number
8
Gene
ERBB2
SIFT Prediction [3]
Deleterious
ClinVar Prediction [3]
Likely pathogenic

ERBB2 S310Y is present in 0.11% of AACR GENIE cases, with bladder urothelial carcinoma, cancer of unknown primary, cervical adenocarcinoma, endocervical carcinoma, and gallbladder carcinoma having the greatest prevalence [4].

Top Disease Cases with ERBB2 S310Y

Significance of ERBB2 S310Y in Diseases

Malignant Solid Tumor +

Breast Carcinoma +

Non-Small Cell Lung Carcinoma +

Cervical Carcinoma +

Urothelial Carcinoma +

Adenocarcinoma Of The Gastroesophageal Junction +

Biliary Tract Carcinoma +

Malignant Uterine Neoplasm +

Gastric Adenocarcinoma +

Gastric Carcinoma +

Breast Adenocarcinoma +

Colorectal Carcinoma +

Non-Squamous Non-Small Cell Lung Carcinoma +

Diffuse Midline Glioma, H3 K27M-Mutant +

Glioblastoma +

WHO Grade III Glioma +

References

1. Hart R and Prlic A. Universal Transcript Archive Repository. Version uta_20180821. San Francisco CA: Github;2015. https://github.com/biocommons/uta

2. The UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Research. 2019;47:D506-D515.

3. Liu X, Wu C, Li C, and Boerwinkle E. dbNSFP v3.0: A one-stop database of functional predictions and annotations for human nonsynonymous and splice site SNVs. Human Mutation. 2015;37:235-241.

Liu X, Jian X, and Boerwinkle E. dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 2011;32:894-899.

4. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.

5. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.