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Art [367]
3 years ago
7

Identify the types of mutations represented by change in each DNA sequence

Biology
2 answers:
ipn [44]3 years ago
5 0

Answer:

below(sorry if i'm wrong, it's been a little while)

Explanation:

deletion

substitution

insertion

inversion

duplication

translocation ?

Simora [160]3 years ago
4 0

PLATO Answer:

deletion

substitution

insertion

inversion

duplication

translocation

Explanation: ATGC → ATC: G is deleted.

ATGC → ATTC: T is substituted for G.

ATTCGC → ATTCGGC: An extra G is inserted.

ACGT → TGCA: The order of bases is inverted, or reversed.

ATTG → ATTGATTG: The bases ATTG are duplicated.

ATTC (chromosome 1) CGATTC (chromosome 2) → ATCGA (chromosome 1) TCTTC (chromosome 2): TC from chromosome 1 translocates to chromosome 2. CGA from chromosome 2 translocates to chromosome 1.

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Explanation:

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7 0
3 years ago
(protein)?
belka [17]

Answer:

Since, the original DNA sequence has not been provided, the mutation can be an insertion/deletion or a frameshift mutation.

  1. Mutated DNA
  2. Frameshift mutation/ insertion or deletion
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Explanation:

Frameshift Mutation:

  • A frameshift mutation is the alteration in the reading frame of the DNA due to the addition/deletion of one or two nucleotides.
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  • The CT at the end of the sequence is indicative of a frameshift in the DNA reading frame.
  • Frameshift mutation affect all amino acids in a polypeptide chain as all codons are moved one or two steps forwards or backwards.
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