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. 2021 May 27;20:106. doi: 10.1186/s12934-021-01598-z

Table 1.

Mutations chosen for detailed characterization

Chromosome Position Mutation Amino acid change Gene Abbreviation
3 286312 C→T Nonsense mutation CDC39 CDC39
10 715141 A→G T200T DAN4 DAN4 T200T
1 27105 A→G T288T FLO9 FLO9 T288T
3 151555 + A Intergenic tK(CUU)C/MAK32 tK(CUU)C/MAK32 int
7 128474 T→A Nonsense mutation MDS3 MDS3
7 404475  + G Intergenic MST27/tR(UCU)G1 MST27/tR(UCU)G1 int
7 530034 A→C S257S MTL1 MTL1 S257S
2 754982 C→T D709N RIF1 RIF1 D709N
9 241053 (A)21→22 Intergenic RNR3/FIS1 RNR3/FIS1 int
14 12986 (T)11→14 Intergenic SNO2/SNZ2 SNO2/SNZ2 int
11 43222 G→T T1025N STE6 STE6 T1025N
1 12690 A→T Intergenic YAL064W-B/TDA8 YAL064W-B/TDA8 int
8 2303 (C)11→12 Intergenic YHL050C/YHL050C YHL050C int

All mutations were verified by Sanger sequencing