If a point mutation occurs in a body cell so that the original sequence of mRNA of CGA changes to AGA, what will be the likely c
onsequence? U
C
A
G
UUU
Phenylalanine
UCU
Serine
UAU
Tyrosine
UGU
Cysteine
U
U
UUC
Phenylalanine
UCC
Serine
UAC
Tyrosine
UGC
Cysteine
C
UUA
Leucine
UCA
Serine
UAA
Stop
UGA
Stop
A
UUG
Leucine
UCG
Serine
UAG
Stop
UGG
Tryptophan
G
CUU
Leucine
CCU
Proline
CAU
Hisitidine
CGU
Arginine
U
C
CUC
Leucine
CCC
Proline
CAC
Hisitidine
CGC
Arginine
C
CUA
Leucine
CCA
Proline
CAA
Glutamine
CGA
Arginine
A
CUG
Leucine
CCG
Proline
CAG
Glutamine
CGG
Arginine
G
AUU
Isoleucine
ACU
Threonine
AAU
Asparagine
AGU
Serine
U
A
AUC
Isoleucine
ACC
Threonine
AAC
Asparagine
AGC
Serine
C
AUA
Isoleucine
ACA
Threonine
AAA
Lysine
AGA
Arginine
A
AUG
Methionine/Start
ACG
Threonine
AAG
Lysine
AGG
Arginine
G
GUU
Valine
GCU
Alanine
GAU
Aspartate
GGU
Glycine
U
G
GUC
Valine
GCC
Alanine
GAC
Aspartate
GGC
Glycine
C
GUA
Valine
GCA
Alanine
GAA
Glutamate
GGA
Glycine
A
GUG
Valine
GCG
Alanine
GAG
Glutamate
GGG
Glycine
G
The mutation will cause a translocation to occur.
The mutation will cause a change in the individual but it will not be inherited.
The mutation will be inherited by the offspring.
The mutation will not cause any change in the individual and it will not be inherited.
If a point mutation occurs during which CGA changes to AGA, the mutation will be simply inherited to the offspring and there won't be any harsh effects on the health of individual.
This is because, both AGA and CGA code for same amino acid called Arginine.
We know that mutations posses harmful effects when they change the genetic sequence leading to the incorporation of incorrect amino acid in the organisms and their offspring. But in this case the mutation will not be harmful and will simply be transferred to the offspring and will have no effect on the functioning, fitness or survival of the organism
