Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g07580 | A07 | 16814801 | G | A | upstream_gene_variant | MODIFIER | c.-4917G>A| |
S163 |
2 | BAA07g07580 | A07 | 16815397 | G | A | upstream_gene_variant | MODIFIER | c.-4321G>A| |
S48 |
3 | BAA07g07580 | A07 | 16816266 | G | A | upstream_gene_variant | MODIFIER | c.-3452G>A| |
S182 |
4 | BAA07g07580 | A07 | 16816304 | C | T | upstream_gene_variant | MODIFIER | c.-3414C>T| |
S181 |
5 | BAA07g07580 | A07 | 16816387 | G | A | upstream_gene_variant | MODIFIER | c.-3331G>A| |
S134 |
6 | BAA07g07580 | A07 | 16820083 | G | A | splice_region_variant&intron_variant | LOW | c.186-4G>A| |
S157 S163 |
7 | BAA07g07580 | A07 | 16820406 | C | T | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S162 |
8 | BAA07g07580 | A07 | 16822015 | G | A | downstream_gene_variant | MODIFIER | c.*1015G>A| |
S134 |
9 | BAA07g07580 | A07 | 16822199 | G | A | downstream_gene_variant | MODIFIER | c.*1199G>A| |
S203 |
10 | BAA07g07580 | A07 | 16823542 | G | A | downstream_gene_variant | MODIFIER | c.*2542G>A| |
S292 |
11 | BAA07g07580 | A07 | 16823674 | G | A | downstream_gene_variant | MODIFIER | c.*2674G>A| |
S62 |
12 | BAA07g07580 | A07 | 16824020 | G | A | downstream_gene_variant | MODIFIER | c.*3020G>A| |
S211 S227 |
13 | BAA07g07580 | A07 | 16824276 | G | T | downstream_gene_variant | MODIFIER | c.*3276G>T| |
S232 |
14 | BAA07g07580 | A07 | 16824282 | G | A | downstream_gene_variant | MODIFIER | c.*3282G>A| |
S177 |
15 | BAA07g07580 | A07 | 16824354 | G | A | downstream_gene_variant | MODIFIER | c.*3354G>A| |
S236 |
16 | BAA07g07580 | A07 | 16825026 | C | T | downstream_gene_variant | MODIFIER | c.*4026C>T| |
S32 |
17 | BAA07g07580 | A07 | 16825028 | G | T | downstream_gene_variant | MODIFIER | c.*4028G>T| |
S76 |
18 | BAA07g07580 | A07 | 16825273 | G | A | downstream_gene_variant | MODIFIER | c.*4273G>A| |
S120 |
19 | BAA07g07580 | A07 | 16825831 | G | T | downstream_gene_variant | MODIFIER | c.*4831G>T| |
S62 |