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B) phosphate

C) base

) polymerase

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Q: What part of a nucleotide accounts for the genetic variation between individuals?
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Related questions

What is the difference between a variation and a mutation?

mutation is an alteration in the nucleotide sequence of a gene whereas variation is any difference between individuals of a particular species.


What is the definition of SNP genotyping?

The definition of SNP genotyping is the measurement of the genetic variation between members of a species. Single nucleotide polymorphisms (SNP) are one of the most common types of genetic variation.


What accounts for the differences between organisms?

The unique base sequence if the individuals dnA


What are commercial accounts used for?

Commercial accounts are for business to business dealings in regards to promoting business and keeping the company sustainable. The commercial accounts contrast with the customer accounts because the business dealings is between companies and not between individuals.


Can allele differ between individuals?

Yes. That accounts for all of the diversity in living things.


Any differences between individuals of the same species?

Of course - look at the many differences existing between the human race.


What does it mean for a gene to be highly conserved?

A conserved gene could mean one of two things: 1. The nucleotide sequence of the gene shows little to no variation between generations 2. The nucleotide sequence of a gene under study shows little to no variation in the genomes of different species, suggesting an evolutionary link. Both definitions are centered around the observation that conserved sequences do not change significantly over time


Which parts in a nucleotide change and what parts stay the same?

A single-nucleotide polymorphism (SNP, pronounced snip) is a DNA sequence variation occurring when a single nucleotide - A, T, C, or G - in the genome (or other shared sequence) differs between members of a species or paired chromosomes in an individual. For example, two sequenced DNA fragments from different individuals, AAGCCTA to AAGCTTA, contain a difference in a single nucleotide. In this case we say that there are two alleles: C and T. Almost all common SNPs have only two alleles.Within a population, SNPs can be assigned a minor allele frequency - the lowest allele frequency at a locus that is observed in a particular population. This is simply the lesser of the two allele frequencies for single-nucleotide polymorphisms. There are variations between human populations, so a SNP allele that is common in one geographical or ethnic group may be much rarer in another.


What is the difference between variety and variation?

What is the difference between variation and variety


What is the difference between nucleotide deletion and nucleotide insertion?

Here's a sample nucleotide sequence:AATUGCIf there was a nucleotide deletion (let's say the "G" gets deleted), the sequence would become:AATUCIf there was a nucleotide addition/insertion (let's say a "G" was added between "T' and "U"), the sequence would become:AATGUGCThe difference is that a deletion makes the DNA shorter and an insertion makes it longer.


What type of chemical bond exits between the two different strands of DNA?

Hydrogen bonding of nucleotide across to nucleotide.


What is the order of size between codon chromosome nucleotide DNA and nucleosome?

this is incorrect question, because the size of the DNA is not specified. Without the DNA, it is chromosome > nucleosome > nucleotide. The actual DNA cannot be longer than a chromosome and nucleotide is a monomer of polymeric DNA, so DNA should be somewhere between chromosome and nucleotide.