synonymous variant variant

Aliases

Syn, Synonymous, synonymous SNV

External links

ClinVar

Related entities (1)

Mentioned in (15)

Papers in which this entity is mentioned.

• Advancing regulatory variant effect prediction with AlphaGenome. (2026)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Immune selection determines tumor antigenicity and influences response to checkpoint inhibitors. (2023)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Establishing guidelines to harmonize tumor mutational burden (TMB): in silico assessment of variation in TMB quantification across diagnostic platforms: phase I of the Friends of Cancer Research TMB Harmonization Project. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
• Mutational processes shape the landscape of TP53 mutations in human cancer. (2018)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• CScape: a tool for predicting oncogenic single-point mutations in the cancer genome. (2017)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)

Merged raw entities (5)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.