MLchartDataset catalogue

Splice-site mutation

Term · Oncology and biomedicine · MLC-T-ONC-007930

A genetic alteration in the DNA sequence that occurs at the boundary of an exon and an intron (splice site). This change can disrupt RNA splicing resulting in the loss of exons or the inclusion of introns and an altered protein-coding sequence. Also called splice-site variant.

Table 1. Record
IdentifierMLC-T-ONC-007930
FieldOncology and biomedicine
Synonymssplice-site variant
ReferencesNCI Dictionary of Genetics Terms
Record as JSON
{
  "id": "MLC-T-ONC-007930",
  "term": "Splice-site mutation",
  "field": "Oncology and biomedicine",
  "definition": "A genetic alteration in the DNA sequence that occurs at the boundary of an exon and an intron (splice site). This change can disrupt RNA splicing resulting in the loss of exons or the inclusion of introns and an altered protein-coding sequence. Also called splice-site variant.",
  "synonyms": [
    "splice-site variant"
  ],
  "references": [
    "NCI Dictionary of Genetics Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/splice-site-mutation/"
}

Record 15,265 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.