Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g32490 | A09 | 41150560 | G | A | downstream_gene_variant | MODIFIER | c.*4797C>T| |
S238 |
2 | BAA09g32490 | A09 | 41151376 | G | A | downstream_gene_variant | MODIFIER | c.*3981C>T| |
S233 |
3 | BAA09g32490 | A09 | 41151907 | G | A | downstream_gene_variant | MODIFIER | c.*3450C>T| |
S124 |
4 | BAA09g32490 | A09 | 41151913 | C | T | downstream_gene_variant | MODIFIER | c.*3444G>A| |
S183 |
5 | BAA09g32490 | A09 | 41152419 | G | A | downstream_gene_variant | MODIFIER | c.*2938C>T| |
S282 |
6 | BAA09g32490 | A09 | 41152453 | C | T | downstream_gene_variant | MODIFIER | c.*2904G>A| |
S245 |
7 | BAA09g32490 | A09 | 41155544 | C | T | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S193 |
8 | BAA09g32490 | A09 | 41155554 | G | A | splice_region_variant&intron_variant | LOW | c.222-3C>T| |
S7 |
9 | BAA09g32490 | A09 | 41157714 | C | T | missense_variant | MODERATE | c.49G>A|p.Ala17Thr |
S8 |
10 | BAA09g32490 | A09 | 41160848 | C | T | upstream_gene_variant | MODIFIER | c.-3086G>A| |
S56 |
11 | BAA09g32490 | A09 | 41160940 | G | A | upstream_gene_variant | MODIFIER | c.-3178C>T| |
S162 |
12 | BAA09g32490 | A09 | 41160967 | C | T | upstream_gene_variant | MODIFIER | c.-3205G>A| |
S159 S243 S299 |
13 | BAA09g32490 | A09 | 41161063 | A | T | upstream_gene_variant | MODIFIER | c.-3301T>A| |
S297 |
14 | BAA09g32490 | A09 | 41161263 | C | T | upstream_gene_variant | MODIFIER | c.-3501G>A| |
S145 |
15 | BAA09g32490 | A09 | 41161490 | C | T | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S18 |
16 | BAA09g32490 | A09 | 41161953 | G | A | upstream_gene_variant | MODIFIER | c.-4191C>T| |
S162 |
17 | BAA09g32490 | A09 | 41162426 | G | A | upstream_gene_variant | MODIFIER | c.-4664C>T| |
S176 |