TP53 NM_000546.5:c.741_742delinsTT

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A complex substitution where the nucleotide sequence at positions 741 and 742 of the coding sequence of the TP53 gene has changed from cytosine-cytosine to thymine-thymine.

**Synonyms:** - LFS1 c.741_742CC>TT - LFS1 c.741_742delCCinsTT - Li-Fraumeni Syndrome c.741_742CC>TT - Li-Fraumeni Syndrome c.741_742delCCinsTT - NM_000546.5:c.741_742CC>TT - NM_000546.5:c.741_742delCCinsTT - NM_000546.5:c.741_742delinsTT - P53 c.741_742CC>TT - P53 c.741_742delCCinsTT - TP53 NM_000546.5:c.741_742CC>TT - TP53 NM_000546.5:c.741_742delCCinsTT - TP53 NM_000546.5:c.741_742delCCinsTT - TP53 c.741_742CC>TT - TP53 c.741_742delCCinsTT - Tumor Protein p53 c.741_742CC>TT - Tumor Protein p53 c.741_742delCCinsTT