Nut cases are arguing with creationists and thinking it is an argument for science.

Creationism VS Evodelusionism is not an argument.

Creationism VS Evodelusionism is not an argument.

Creationism VS Evodelusionism is not an argument.

Creationism VS Evodelusionism is not an argument.....................................

There is no science in delusions.

DNA evidence is absolutely irrefutable physical evidence that evolution has never taken place.

There are no improvements shown in any DNA study, only continual degradation of the genomes.

If you don't understand that, it is because you are ignorant, brainwashed, religious nut case.

The Chimp, Gorilla, Orangutan, Macaque are all from the same genetic lineage as humans.  This is clearly in the DNA evidence. All have degraded genetically over the many years.  They have not improved. Neither have humans.

If you want to see what happens to the human genome when radiation and lifestyle eats away at the cell replication and destroys the DNA sequences that produce healthy cells, look at the chimp, gorilla, orangutan,and macaque. Tremendous genetic losses are shown in these creatures because they lived in volcanic regions with high levels of natural radiation.


There is no "magical mutations" that fixes screwed up genomics.  70% of the mutations are bad, deleterious and
29% are considered neutral with 1% "Might be" helpful.

There is no net evolution towards more fit, more complex, nor more healthy.  All creatures are heading towards extinction, the natural result of diminished genetic coding.

The best we can do is to preserve our genome so that our descendants are not unintelligent retards scraping the ground for food until the entire species dies out.

Chimps, Gorillas, Orangutans are all going extinct. They do not have the skills, nor health, necessary to survive much longer. The message is clear in the DNA and what has happened to them is a message for us.

They have diabetes, heart disease, cancer, shortening lifespan and many of the illnesses we are  rapidly progressing towards as our genome is being destroyed by constant electromagnetic radiation, bad lifestyles and not using much of our existing survival genetics. 

Don't be stupid and believe in magical nonsense. Follow the evidence. It is clear, cannot be denied, unless you  keep your head in the sand of ridiculous beliefs having no foundation other than your religious mythology.   

These are quotes from the US government site on genetics.
When something that was working fine and has a mutation, then the odds are 70 to 1 that it is deleterious, according to degreed, PHD's of genetics.
There are mechanisms that repair DNA, (thank God!) but if those mechanisms are screwed up because they are controlled by DNA, then some really bad diseases happen.

Point Mutation
A point mutation is a simple change in one base of the gene sequence. This is equivalent to changing one letter in a sentence, such as this example, where we change the 'c' in cat to an 'h':

Original

The fat cat ate the wee rat.

Point Mutation      The fat hat ate the wee rat.
(Sickle Cell Anemia is a point mutation that modified one base pair.)

Frame-shift mutation
Frame-shift mutations. In a frame shift mutation, one or more bases are inserted or deleted, the equivalent of adding or removing letters in a sentence. But because our cells read DNA in three letter "words", adding or removing one letter changes each subsequent word. This type of mutation can make the DNA meaningless and often results in a shortened protein. An example of a frame-shift mutation using our sample sentence is when the 't' from cat is removed, but we keep the original letter spacing:

Original

The fat cat ate the wee rat.

Frame Shift      The fat caa tet hew eer at.

(Frame shift is horrible for any complex creature with multi-cells. For bacteria,(single cell creatures) for instance, it either kills it or it lives to eat more carbon based foods.)

Deletion
Mutations that result in missing DNA are called deletions. These can be small, such as the removal of just one "word," or longer deletions that affect a large number of genes on the chromosome. Deletions can also cause frameshift mutations. In this example, the deletion eliminated the word cat.

Original

The fat cat ate the wee rat.

Deletion      The fat ate the wee rat.
( Consider that you need that protean to make cells which make body parts. When the codon is gone, there is no protean being produced.)

Insertion
Mutations that result in the addition of extra DNA are called insertions. Insertions can also cause frameshift mutations, and general result in a nonfunctional protein.

(NOTE:  "nonfunctional protean".)

Original

The fat cat ate the wee rat.

Insertion      The fat cat xlw ate the wee rat.
Inversion
In an inversion mutation, an entire section of DNA is reversed. A small inversion may involve only a few bases within a gene, while longer inversions involve large regions of a chromosome containing several genes.

Original

The fat cat ate the wee rat.

Insertion      The fat tar eew eht eta tac.
DNA expression mutation
There are many types of mutations that change not the protein itself but where and how much of a protein is made. These types of changes in DNA can result in proteins being made at the wrong time or in the wrong cell type. Changes can also occur that result in too much or too little of the protein being made.

(What part of this is good? Duh!  NONE!)


Here are all the types of mutations from US gov genetics site:
"Missense mutation
This type of mutation is a change in one DNA base pair that results in the substitution of one amino acid for another in the protein made by a gene."

If you have correct cell reproduction, you don't with this. The cell is reduced in its function or it atrophies.


"Nonsense mutation
A nonsense mutation is also a change in one DNA base pair. Instead of substituting one amino acid for another, however, the altered DNA sequence prematurely signals the cell to stop building a protein. This type of mutation results in a shortened protein that may function improperly or not at all."

If you had a good cell replication this certainly will screw it up and cause it to atrophy. You cannot build healthy cells with messed up DNA and short of a needed protean. 


"Insertion
An insertion changes the number of DNA bases in a gene by adding a piece of DNA. As a result, the protein made by the gene may not function properly."

If you have an insertion, the protean that was being made is not made the way it was originally.  This is almost always detrimental.


Deletion
A deletion changes the number of DNA bases by removing a piece of DNA. Small deletions may remove one or a few base pairs within a gene, while larger deletions can remove an entire gene or several neighboring genes. The deleted DNA may alter the function of the resulting protein(s)."

If you delete the proper coding for say a lung cell, what do you think will happen?  It diminishes in its function and has a "genetic disease".  Normal cell reproduction is reduced or completely flawed.


"Duplication

A duplication consists of a piece of DNA that is abnormally copied one or more times. This type of mutation may alter the function of the resulting protein."

This is sometimes neutral, but most of the time harmful because you have an extra protean that is not needed.


"Frameshift mutation

This type of mutation occurs when the addition or loss of DNA bases changes a gene’s reading frame. A reading frame consists of groups of 3 bases that each code for one amino acid. A frameshift mutation shifts the grouping of these bases and changes the code for amino acids. The resulting protein is usually nonfunctional. Insertions, deletions, and duplications can all be frameshift mutations."

Frameshifts are almost always harmful to cell reproduction.


Repeat expansion (illustration)
Nucleotide repeats are short DNA sequences that are repeated a number of times in a row. For example, a trinucleotide repeat is made up of 3-base-pair sequences, and a tetranucleotide repeat is made up of 4-base-pair sequences. A repeat expansion is a mutation that increases the number of times that the short DNA sequence is repeated. This type of mutation can cause the resulting protein to function improperly.

Any sane person can see that mutations are not something we want.

We just want our cells to replicate as strong good performing cells, giving us health. But as we progress along the path of self destruction, we are not getting that. There are over 4000 and counting defective DNA codings we have identified so far according the the "Human Genome Project's" head honcho.

The news is not good for humanity.  Self destruction is what we seem to want in our ignorance. 

I am trying very hard to stop this delusional idea that by "magic" our genome will fix all the defects and genetic illnesses.  That is not going to happen without some serious help from the "genetic engineer" who designed us.

We can stop much of it by reducing the causes for the levels of genetic defects we have now.  Continue to interbreed out some of the defects with others who have healthy "complimentary" parts to our defects and pair up with those who are stronger in areas where we are weak.

http://www.ncbi.nlm.nih.gov/pubmed?term=Gene%20loss
There are over 85,000 papers just on gene loss and disease on this PubMed site.