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GENETIC MARKER
SINGLE NUCLEOTIDE
POLYMORPHISM
(SNP)
by
Saloni Arora
SNP
GCAT
A Genetic marker is a gene or
DNA sequence with a known
location on chromosome that
can be used to identify
individuals or species.
A genetic marker may be a
short DNA sequence
surrounding a single base-pair
change ( SNP ), or a long one
like, minisatellites.
SNP
GCAT
http://isaaa.org/siteimages/pocketkimages
/clip_image002_0018.jpg
The world polymorphism is a generic term that
means “many shapes” i.e. ability to appear in
different forms .
SNP is defined as a single base change in DNA
sequence that occurs in a significant proportion (
more than 1% ) of a large population .
SNP
GCAT
Human genome sequence
is 99.9% identical in all
people .
However , there are certain
positions (Fig.1) where
some people have one
nucleotide pair , while others
have another
These positions are known
as SNPs .
www. learn.genetics.com
SNPs are the most frequent forms
among various genetic variations .
> 90% of human genetic
variations come from SNPs.
 SNP has become preferred markers
for association studies .
SNP
GCAT
 The nucleotide on SNP locus is called
> a major allele
> a minor allele
94% ---- A C T T A G C T G - G : major allele
6% ---- A C T T A G C T T - T: minor allele
http://projects.nfstc.org/pdi/Subject09/images/pdi_s09_m02_01_c.jpg
SNP
GCAT
Non-coding region
Coding region
NON-CODING REGION
A segment of DNA that does comprise a gene and thus does
not code for a protein .
SNP
GCAT
CODING REGION
Regions of DNA/RNA sequence that
code for proteins
SYNONYMOUS
A SNP in which both forms lead to the same polypeptide
sequence is called synonymous .
( sometimes called silent mutations )
NON-SYNONYMOUS
If a different polypeptide sequence is produced they are non
synonymous .
A non synonymous change may either be missense or
nonsense
• a missense change results in a different amino acid .
• a nonsense change results in a premature stop codon .
SNP
GCAT
SNP
GCAT
http://learn.genetics.utah.edu/content/precision/snips/images/snp-types.jpg
For a variation to be considered a SNP, it
must occur in at least 1% of the population.
They occur once in every 300~600
nucleosides on average , which means 10
million SNPs in the human genome .
Most commonly these variations are found in
DNA between genes .
SNP
GCAT
Personalized
medicines
Genetic marker
Human genetic study
SNP
GCAT
Sequence genomes of a large number of
people.
Compare the base sequences to discover
SNPs.
Generate a single map of the human
genome containing all possible SNPs => SNP
maps.
SNP
GCAT
SNP
GCAT
http://www.ubooks.pub/Books/B0/E19R191
9/MAIN/images/image036.jpg
Genome of each individual contain
distinct SNP pattern .
People can be grouped based on SNP
profile.
SNPs profiles are important for
identifying response to drug therapy.
There might be correlations between
certain SNP profiles and specific
responses to treatments .
SNP
GCAT
SNP
GCAT
.http://www.ubooks.pub/Books/B0/E19R
1919/MAIN/images/image037.jpg
 Primer extension is a method scientists used to
determine which version of known SNP a person has .
SNP
GCAT
http://isaaa.org/siteimages/pocketkimages/clip002_0018.jpg
Anyone may obtain a SNP report from
several on-line genome scanning
companies .
 SNP detection technologies are used
to scan for new polymorphism and to
determine the allele(s) of a known
polymorphism in target sequences .
SNP
GCAT
SNP
GCAT
MAY BE HARMLESS
. Change in phenotype
. Pigmentation
. Livestock breeding programs
MAY BE HARMFUL
. Diabetes , cancer
. Parkinson’s disease
. Huntington’s disease
SNP
GCAT
Evolution and ecological genomics
Gene discovery and mapping
Response prediction
Homogeneity testing / study design
Gene function identification
Association based candidate polymorphism
testing
Diagnostics / risk profiling
Drug discovery and development
SNP
GCAT
“SNPs and snails and puppy dog tails, and
that’s what people are made of …”
A Case Study on Genome Privacy
by
Debby Walser -Kuntz, Sarah Deel, and Susan Singer
Department of Biology
Carleton College, Northfield, MN
In April 1999 Terri Seargent went to her doctor with slight
breathing difficulties. A simple genetic test confirmed her worst
nightmare: she had alpha-1 deficiency, meaning that she might
one day succumb to the same respiratory disease that killed her
brother. The test probably saved Seargent’s life—the condition is
treatable if detected early—but when her employer learned of her
costly condition, she was fired and lost her health insurance.
SNP
GCAT
There are privacy issues with genetic Information .
Concerned scientists have requested to pass laws
that protect employees .
Over the past few years, many proposed bills failed .
One current piece of federal legislation being
considered by the U.S. House of Representatives is the
Genetic Information Nondiscrimination Act.
The following are key excerpts from the Act:
Use of Genetic Information
Acquisition of Genetic Information
 where an employer purchases documents
that are commercially and publicly available
that include family medical history.
SNP
GCAT
Single-nucleotide polymorphism / SNP | Learn
Science at Scitable .
Human Genome Project Information — SNP Fact
Sheet
http://www.ncbi.nlm.nih.gov/About/primer/snps.html
Carlson, Bruce (2008-06-15). "SNPs — A Shortcut
to Personalized Medicine". Genetic Engineering &
Biotechnology News. Mary Ann Liebert, Inc. 28 (12).
Retrieved 2008-07-06.
www.nature.com
www.pubmedcentral.gov.in
SNP
GCAT
Snp

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Snp

  • 2. A Genetic marker is a gene or DNA sequence with a known location on chromosome that can be used to identify individuals or species. A genetic marker may be a short DNA sequence surrounding a single base-pair change ( SNP ), or a long one like, minisatellites. SNP GCAT http://isaaa.org/siteimages/pocketkimages /clip_image002_0018.jpg
  • 3. The world polymorphism is a generic term that means “many shapes” i.e. ability to appear in different forms . SNP is defined as a single base change in DNA sequence that occurs in a significant proportion ( more than 1% ) of a large population . SNP GCAT
  • 4. Human genome sequence is 99.9% identical in all people . However , there are certain positions (Fig.1) where some people have one nucleotide pair , while others have another These positions are known as SNPs . www. learn.genetics.com
  • 5. SNPs are the most frequent forms among various genetic variations . > 90% of human genetic variations come from SNPs.  SNP has become preferred markers for association studies . SNP GCAT
  • 6.  The nucleotide on SNP locus is called > a major allele > a minor allele 94% ---- A C T T A G C T G - G : major allele 6% ---- A C T T A G C T T - T: minor allele http://projects.nfstc.org/pdi/Subject09/images/pdi_s09_m02_01_c.jpg SNP GCAT
  • 7. Non-coding region Coding region NON-CODING REGION A segment of DNA that does comprise a gene and thus does not code for a protein . SNP GCAT
  • 8. CODING REGION Regions of DNA/RNA sequence that code for proteins SYNONYMOUS A SNP in which both forms lead to the same polypeptide sequence is called synonymous . ( sometimes called silent mutations ) NON-SYNONYMOUS If a different polypeptide sequence is produced they are non synonymous . A non synonymous change may either be missense or nonsense • a missense change results in a different amino acid . • a nonsense change results in a premature stop codon . SNP GCAT
  • 10. For a variation to be considered a SNP, it must occur in at least 1% of the population. They occur once in every 300~600 nucleosides on average , which means 10 million SNPs in the human genome . Most commonly these variations are found in DNA between genes . SNP GCAT
  • 12. Sequence genomes of a large number of people. Compare the base sequences to discover SNPs. Generate a single map of the human genome containing all possible SNPs => SNP maps. SNP GCAT
  • 14. Genome of each individual contain distinct SNP pattern . People can be grouped based on SNP profile. SNPs profiles are important for identifying response to drug therapy. There might be correlations between certain SNP profiles and specific responses to treatments . SNP GCAT
  • 16.  Primer extension is a method scientists used to determine which version of known SNP a person has . SNP GCAT http://isaaa.org/siteimages/pocketkimages/clip002_0018.jpg
  • 17. Anyone may obtain a SNP report from several on-line genome scanning companies .  SNP detection technologies are used to scan for new polymorphism and to determine the allele(s) of a known polymorphism in target sequences . SNP GCAT
  • 19. MAY BE HARMLESS . Change in phenotype . Pigmentation . Livestock breeding programs MAY BE HARMFUL . Diabetes , cancer . Parkinson’s disease . Huntington’s disease SNP GCAT
  • 20. Evolution and ecological genomics Gene discovery and mapping Response prediction Homogeneity testing / study design Gene function identification Association based candidate polymorphism testing Diagnostics / risk profiling Drug discovery and development SNP GCAT
  • 21. “SNPs and snails and puppy dog tails, and that’s what people are made of …” A Case Study on Genome Privacy by Debby Walser -Kuntz, Sarah Deel, and Susan Singer Department of Biology Carleton College, Northfield, MN In April 1999 Terri Seargent went to her doctor with slight breathing difficulties. A simple genetic test confirmed her worst nightmare: she had alpha-1 deficiency, meaning that she might one day succumb to the same respiratory disease that killed her brother. The test probably saved Seargent’s life—the condition is treatable if detected early—but when her employer learned of her costly condition, she was fired and lost her health insurance. SNP GCAT
  • 22. There are privacy issues with genetic Information . Concerned scientists have requested to pass laws that protect employees . Over the past few years, many proposed bills failed . One current piece of federal legislation being considered by the U.S. House of Representatives is the Genetic Information Nondiscrimination Act. The following are key excerpts from the Act: Use of Genetic Information Acquisition of Genetic Information  where an employer purchases documents that are commercially and publicly available that include family medical history. SNP GCAT
  • 23. Single-nucleotide polymorphism / SNP | Learn Science at Scitable . Human Genome Project Information — SNP Fact Sheet http://www.ncbi.nlm.nih.gov/About/primer/snps.html Carlson, Bruce (2008-06-15). "SNPs — A Shortcut to Personalized Medicine". Genetic Engineering & Biotechnology News. Mary Ann Liebert, Inc. 28 (12). Retrieved 2008-07-06. www.nature.com www.pubmedcentral.gov.in SNP GCAT