Single Nucleotide Polymorphism;

Last updated on: 23.07.2021

Dieser Artikel auf Deutsch

This section has been translated automatically.

Single nucleotide polymorphism (SNP) refers to a variation of a single base pair (single nucleotides) in DNA. It is the smallest heritable genetic unit. A single nucleotide polymorphism can be used to explain interindividual genetic differences.

The human genome has about 6 billion base pairs, of which about 3.3 million are interindividual variations, i.e. SNPs. SNPs usually have no effect on the function of the gene, but they do provide information about the genetic basis of diseases. Since they are relatively easy to detect - the genome does not have to be sequenced for this - many medical studies are based on their analysis.

About 38 million SNPs are found in the human genome. About one in five hundred DNA bases may be altered. Some are common, but others are found in less than 1% of the population. SNPs are also known as "successful point mutations", i.e. genetic changes that have become established to some degree in the gene pool of a population, and have thus become heritable changes.

General information
This section has been translated automatically.

SNPs do not occur evenly distributed, but rather unevenly at specific regions. In an estimated two-thirds of all cases, a C>T exchange is found, which is often due to the deamination of a methylated cytosine (5-methylcytosine) to thymine.

The SNPs are found in both coding and non-coding intronic regions.

The majority of SNPs are silent or synonymous. Silent SNPs do not alter the amiso acid sequence derived from them.

Non-synonymous SNPs (approximately 100,000) result in an altered amino acid sequence. SNPs can occur in the coding or non-coding region of the genome. If SNPs are located in a non-coding region of the genome, this single nucleotide polymorphism may also have an effect on gene transcription depending on its placement (regulatory SNPs).

Diagnosis: Methods for the identification of single nucleotide polymorphisms are e.g. DNA sequencing, microarrays and, in combination with allele-specific oligonucleotides, polymerase chain reaction and isothermal DNA amplification.

This section has been translated automatically.

From biomedical research, SNPs have become irreplaceable. They allow the mapping of the genome. On the one hand, SNPs can be assigned a fixed position in the genome, and on the other hand, they are inherited together with the surrounding genes. Thus, if individual SNPs occur particularly frequently together with any congenital traits, one can draw conclusions about the genes that may be involved. The SNP variants are listed in the SNP database (dbSNP) under defined reference numbers and with additional information on frequency, allele distribution and genomic characteristics.

Incoming links (1)


Last updated on: 23.07.2021