Lobster claw syndrome, or Ectrodactyly, is a rare genetic condition caused by a mutation in the TP63 gene, which is inherited in an autosomal dominant pattern. This means that only one copy of the mutated gene is needed to display the syndrome.
A one base left out mutation is called a deletion mutation. This type of mutation involves the loss of one or more nucleotides from a DNA sequence, which can lead to a frameshift mutation if not in multiples of three.
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
Frameshift mutation.
transcription
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
It is a mutation/
chromosomal mutation
deletion mutation
Lobster claw syndrome, or Ectrodactyly, is a rare genetic condition caused by a mutation in the TP63 gene, which is inherited in an autosomal dominant pattern. This means that only one copy of the mutated gene is needed to display the syndrome.
A mutation that involves a single nucleotide is called a point mutation. This type of mutation can include substitutions, insertions, or deletions of a single nucleotide in the DNA sequence.
A frameshift mutation in the CARD15 gene
A one base left out mutation is called a deletion mutation. This type of mutation involves the loss of one or more nucleotides from a DNA sequence, which can lead to a frameshift mutation if not in multiples of three.
No, the fusion of the two middle toes is not indicative of ectrodactyly. Ectrodactyly, also known as lobster claw deformity, is a more severe condition where there is a missing or cleft hand or foot due to a congenital malformation. Fusion of toes may be due to other causes.
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
Chromosomal mutation
a point mutation