Snv Samenvattingen, Aantekeningen en Examens

Types of DNA Variation - single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) AUG (methionine) Stop Codons UGA, UAA, UAG

CMMB 413 Exam with 100% Correct Answers | Verified | Latest 2024 Version Types of DNA Variation - single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) AUG (methionine) Stop Codons UGA, UAA, UAG 20 number of amino acids 64 number of dif...

SNV Correct Answer: Any sequence change that affects one base of genome SNPs are common ones Promoter Correct Answer: specific region of a gene where RNA polymerase can bind and begin transcription Nucleosome Correct Answer: 150 bps of DNA around core proteins Stop Codons Correct Answer: UAA, UAG, UGA Karyotype Analysis Correct Answer: Usually done at metaphase Detects trisomy, deletions, duplications, translocations Confirming test FISH Analysis Correct Answer: Fluores...

HMX Genetics Exam Questions with Correct Answers Single Nucleotide Variant (SNV) - ANSWER differences in DNA sequence. 46 chromosomes. >1% of population. Common complex traits bp in nucleus - ANSWER 6 billion Chromatin - ANSWER packaged DNA. Composed of DNA helix wound around histone proteins forming nucleosomes. 150 bp of DNA wound around each histone core Amino acid - ANSWER 20 different molecules used to build proteins. Coded by genes. Organic. Contains...

CMMB 413 Final Exam Review Actual Questions and Answers Solved 100% Types of DNA Variation - answer- single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - answer- most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) - answerAUG (methionine) Stop Codons - answerUGA, UAA, UAG 20 - answernumb...

CMMB 413 Final Exam Review 2024 Update| Questions with Complete Solutions| Certified Quality Guaranteed Success Types of DNA Variation - single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) AUG (methionine) Stop Codons UGA, UAA, UAG...

HMX Genetics Practice Test Questions and Answers Variants - ANSWER Differences in DNA sequence -lead to changes in phenotype -can affect amount of RNA produced by affecting transcription, RNA stability, changing RNA levels -can affect amount of protein produced by affecting translation, protein stability, changing protein levels, protein function, etc. Single Nucleotide Variance (SNV) - ANSWER differences in DNA sequence at one location Single Nucleotide Polymorphisms ...

HMX Genetics Test Questions with Correct Answers SNV - ANSWER Any sequence change that affects one base of genome SNPs are common ones Promoter - ANSWER specific region of a gene where RNA polymerase can bind and begin transcription Nucleosome - ANSWER 150 bps of DNA around core proteins Stop Codons - ANSWER UAA, UAG, UGA Karyotype Analysis - ANSWER Usually done at metaphase Detects trisomy, deletions, duplications, translocations Confir...