Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26110 | A04 | 26877607 | G | A | downstream_gene_variant | MODIFIER | c.*3976C>T| |
S108 |
2 | BAA04g26110 | A04 | 26878770 | C | T | downstream_gene_variant | MODIFIER | c.*2813G>A| |
S192 |
3 | BAA04g26110 | A04 | 26880320 | G | A | downstream_gene_variant | MODIFIER | c.*1263C>T| |
S257 |
4 | BAA04g26110 | A04 | 26880728 | G | A | downstream_gene_variant | MODIFIER | c.*855C>T| |
S82 S92 |
5 | BAA04g26110 | A04 | 26881444 | G | A | downstream_gene_variant | MODIFIER | c.*139C>T| |
S53 |
6 | BAA04g26110 | A04 | 26881728 | C | T | intron_variant | MODIFIER | c.688-95G>A| |
S112 |
7 | BAA04g26110 | A04 | 26881856 | G | A | intron_variant | MODIFIER | c.688-223C>T| |
S190 |
8 | BAA04g26110 | A04 | 26882144 | G | A | intron_variant | MODIFIER | c.687+409C>T| |
S85 |
9 | BAA04g26110 | A04 | 26882645 | C | T | missense_variant | MODERATE | c.595G>A|p.Glu199Lys |
S42 |
10 | BAA04g26110 | A04 | 26883786 | G | A | missense_variant | MODERATE | c.452C>T|p.Ser151Phe |
S138 |
11 | BAA04g26110 | A04 | 26884126 | C | T | missense_variant | MODERATE | c.112G>A|p.Glu38Lys |
S247 |
12 | BAA04g26110 | A04 | 26885110 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| |
S284 |
13 | BAA04g26110 | A04 | 26887565 | C | T | upstream_gene_variant | MODIFIER | c.-3328G>A| |
S125 |
14 | BAA04g26110 | A04 | 26888855 | C | T | upstream_gene_variant | MODIFIER | c.-4618G>A| |
S51 |