Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g05380 | A05 | 2624897 | C | T | upstream_gene_variant | MODIFIER | c.-264C>T| |
S174 S27 |
2 | BAA05g05380 | A05 | 2624927 | C | T | upstream_gene_variant | MODIFIER | c.-234C>T| |
S228 |
3 | BAA05g05380 | A05 | 2625663 | C | T | synonymous_variant | LOW | c.411C>T|p.Ala137Ala |
S297 |
4 | BAA05g05380 | A05 | 2626047 | G | A | synonymous_variant | LOW | c.795G>A|p.Lys265Lys |
S132 S137 S215 S89 |
5 | BAA05g05380 | A05 | 2627622 | C | T | missense_variant | MODERATE | c.1979C>T|p.Pro660Leu |
S28 |
6 | BAA05g05380 | A05 | 2629044 | G | A | missense_variant | MODERATE | c.3112G>A|p.Glu1038Lys |
S206 S26 |
7 | BAA05g05380 | A05 | 2629468 | G | A | splice_region_variant&synonymous_variant | LOW | c.3462G>A|p.Gly1154Gly |
S264 |
8 | BAA05g05380 | A05 | 2629750 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3667-1G>A| |
S306 S308 |
9 | BAA05g05380 | A05 | 2630774 | G | A | missense_variant | MODERATE | c.4444G>A|p.Ala1482Thr |
S144 |
10 | BAA05g05380 | A05 | 2634993 | G | A | downstream_gene_variant | MODIFIER | c.*3431G>A| |
S246 |
11 | BAA05g05380 | A05 | 2635294 | C | T | downstream_gene_variant | MODIFIER | c.*3732C>T| |
S155 S211 |
12 | BAA05g05380 | A05 | 2635576 | G | A | downstream_gene_variant | MODIFIER | c.*4014G>A| |
S37 |
13 | BAA05g05380 | A05 | 2635580 | G | A | downstream_gene_variant | MODIFIER | c.*4018G>A| |
S138 |