A premature stop codon (C-T mutation) disrupting base 2065 of the coding sequence (CDS), which locates in the conserved Helicase_C_2 domain.
Amino acid replacement: Q689term.
Nucleotide substitution: C2065T.
C5750203T
C2065T
Q689term | Rtel1-PA; Q689term | Rtel1-PB
Q689term
Rtel1xp171 is rescued by Rtel1fTRG01096.sfGFP-TVPTBF