How many locations have been identified in the human genome where single base differences occur?
- A$1.4$ million
- B$14$ million
- C$1.4$ billion
- D$14$ billion
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Similar Questions
Correctly match Column-$I$ with Column-$II$ regarding $\text{H.G.P.}:-$
Column-$I$ Column-$II$ $A$. $1^{st}$ Chromosome $i$. $1.4$ million locations $B$. $\text{SNPs}$ $ii$. $2968$ genes $C$. Dystrophin gene $iii$. $Y$ Chromosome $D$. $\text{TDF}$ gene $iv$. $2.4$ million $bp$
| Column-$I$ | Column-$II$ |
| $A$. $1^{st}$ Chromosome | $i$. $1.4$ million locations |
| $B$. $\text{SNPs}$ | $ii$. $2968$ genes |
| $C$. Dystrophin gene | $iii$. $Y$ Chromosome |
| $D$. $\text{TDF}$ gene | $iv$. $2.4$ million $bp$ |
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View SolutionWhich of the following is $NOT$ a goal of the $HGP$?
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View SolutionThe human genome contains .......... base pairs.
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View SolutionThe main aim of the Human Genome Project is
What was used as a host in the $HGP$?
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