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. 2014 Dec 30;10:41. doi: 10.1186/s13007-014-0041-7

Table 2.

Candidate causative SNPs in bak1 - 5 mob1

Chr Position Ref/Alt AF (%) AGI Gene ID AA change Sanger F 3
1 11892068 C/T 100 At1g32830 Transposable element n.a. Absent
1 11892070 G/T 100 At1g32830 Transposable element n.a. Homa
1 11892252 T/G 100 At1g32830 Transposable element n.a. Homa
1 16516501 T/C 83.3 At1g43745 Transposable element n.a. Absent
1 16525522 T/C 77.8 At1g43755 Transposable element n.a. Homa
1 24243231 G/A 80.9 At1g65270 Unknown protein G > S Hom
5 26457834 G/A 85.0 At5g66210 CPK28 A > V Homb
5 26458077 G/A 78.5 At5g66210 CPK28 S > L Homb
5 26474069 G/A 76.5 At5g66270 Zn-finger family protein P > L Hom

Unique SNPs in annotated coding regions with allele frequencies (AF) over 75% identified by CandiSNP for bak1-5 mob1, listing the Chromosome number (Chr), position, reference base (Ref), sequenced alternate base (Alt), locus number (AGI), gene identification (Gene ID), amino acid change (AA change; ‘n.a.’ is not applicable). All SNPs were confirmed in at least three independent back-crossed lines (F3 generation) by Sanger sequencing compared to bak1-5. SNPs that were homozygous (Hom) or not present (Absent) are listed.

aThese SNPs were also identified in bak1-5 by Sanger sequencing (however, not by Illumina sequencing) and are therefore not unique to bak1-5 mob1.

bThese SNPs are the causative mutations for bak1-5 mob1 [13].