Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17290 | A05 | 9710380 | G | A | missense_variant | MODERATE | c.221C>T|p.Ser74Phe |
S279 |
2 | BAA05g17290 | A05 | 9710987 | G | A | intron_variant | MODIFIER | c.140-526C>T| |
S180 |
3 | BAA05g17290 | A05 | 9712070 | G | A | intron_variant | MODIFIER | c.140-1609C>T| |
S157 |
4 | BAA05g17290 | A05 | 9712384 | C | T | intron_variant | MODIFIER | c.140-1923G>A| |
S50 |
5 | BAA05g17290 | A05 | 9712385 | C | T | intron_variant | MODIFIER | c.140-1924G>A| |
S45 |
6 | BAA05g17290 | A05 | 9713482 | G | A | intron_variant | MODIFIER | c.139+2807C>T| |
S94 |
7 | BAA05g17290 | A05 | 9715632 | G | A | intron_variant | MODIFIER | c.139+657C>T| |
S308 |
8 | BAA05g17290 | A05 | 9715883 | G | A | intron_variant | MODIFIER | c.139+406C>T| |
S170 |
9 | BAA05g17290 | A05 | 9716902 | C | T | upstream_gene_variant | MODIFIER | c.-387G>A| |
S140 S279 |
10 | BAA05g17290 | A05 | 9717214 | C | T | upstream_gene_variant | MODIFIER | c.-699G>A| |
S228 |
11 | BAA05g17290 | A05 | 9717960 | G | A | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S127 |
12 | BAA05g17290 | A05 | 9718313 | G | A | upstream_gene_variant | MODIFIER | c.-1798C>T| |
S243 S299 |
13 | BAA05g17290 | A05 | 9721198 | C | T | upstream_gene_variant | MODIFIER | c.-4683G>A| |
S17 |