Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g09170 | A03 | 3796797 | C | T | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S245 |
2 | BAA03g09170 | A03 | 3797353 | G | A | upstream_gene_variant | MODIFIER | c.-2042G>A| |
S70 |
3 | BAA03g09170 | A03 | 3797418 | G | A | upstream_gene_variant | MODIFIER | c.-1977G>A| |
S210 |
4 | BAA03g09170 | A03 | 3798157 | C | T | upstream_gene_variant | MODIFIER | c.-1238C>T| |
S179 |
5 | BAA03g09170 | A03 | 3798403 | G | A | upstream_gene_variant | MODIFIER | c.-992G>A| |
S47 |
6 | BAA03g09170 | A03 | 3799901 | C | T | intron_variant | MODIFIER | c.128-55C>T| |
S266 |
7 | BAA03g09170 | A03 | 3799930 | C | T | intron_variant | MODIFIER | c.128-26C>T| |
S19 |
8 | BAA03g09170 | A03 | 3800936 | C | T | missense_variant | MODERATE | c.851C>T|p.Thr284Ile |
S293 |
9 | BAA03g09170 | A03 | 3801334 | C | T | missense_variant | MODERATE | c.1112C>T|p.Ala371Val |
S230 |