Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40580 | A01 | 26875836 | T | C | downstream_gene_variant | MODIFIER | c.*4985A>G| |
S19 S305 |
2 | BAA01g40580 | A01 | 26875837 | C | T | downstream_gene_variant | MODIFIER | c.*4984G>A| |
S94 |
3 | BAA01g40580 | A01 | 26875871 | G | A | downstream_gene_variant | MODIFIER | c.*4950C>T| |
S58 |
4 | BAA01g40580 | A01 | 26876186 | C | T | downstream_gene_variant | MODIFIER | c.*4635G>A| |
S12 |
5 | BAA01g40580 | A01 | 26876802 | C | T | downstream_gene_variant | MODIFIER | c.*4019G>A| |
S251 |
6 | BAA01g40580 | A01 | 26877113 | G | A | downstream_gene_variant | MODIFIER | c.*3708C>T| |
S241 |
7 | BAA01g40580 | A01 | 26877199 | C | T | downstream_gene_variant | MODIFIER | c.*3622G>A| |
S118 |
8 | BAA01g40580 | A01 | 26877775 | C | T | downstream_gene_variant | MODIFIER | c.*3046G>A| |
S267 |
9 | BAA01g40580 | A01 | 26878031 | C | T | downstream_gene_variant | MODIFIER | c.*2790G>A| |
S292 |
10 | BAA01g40580 | A01 | 26878617 | T | A | downstream_gene_variant | MODIFIER | c.*2204A>T| |
S206 S26 |
11 | BAA01g40580 | A01 | 26878678 | C | T | downstream_gene_variant | MODIFIER | c.*2143G>A| |
S20 |
12 | BAA01g40580 | A01 | 26879155 | C | T | downstream_gene_variant | MODIFIER | c.*1666G>A| |
S32 |
13 | BAA01g40580 | A01 | 26879402 | C | T | downstream_gene_variant | MODIFIER | c.*1419G>A| |
S37 |
14 | BAA01g40580 | A01 | 26879720 | C | T | downstream_gene_variant | MODIFIER | c.*1101G>A| |
S32 |
15 | BAA01g40580 | A01 | 26879922 | G | A | downstream_gene_variant | MODIFIER | c.*899C>T| |
S208 S219 |
16 | BAA01g40580 | A01 | 26880134 | G | A | downstream_gene_variant | MODIFIER | c.*687C>T| |
S202 |
17 | BAA01g40580 | A01 | 26880669 | C | T | downstream_gene_variant | MODIFIER | c.*152G>A| |
S237 |
18 | BAA01g40580 | A01 | 26880998 | C | T | intron_variant | MODIFIER | c.639+33G>A| |
S161 |
19 | BAA01g40580 | A01 | 26881307 | G | A | synonymous_variant | LOW | c.456C>T|p.Asn152Asn |
S298 |
20 | BAA01g40580 | A01 | 26881460 | G | A | intron_variant | MODIFIER | c.343-40C>T| |
S157 S163 |
21 | BAA01g40580 | A01 | 26882303 | C | T | upstream_gene_variant | MODIFIER | c.-444G>A| |
S293 |
22 | BAA01g40580 | A01 | 26884707 | G | A | upstream_gene_variant | MODIFIER | c.-2848C>T| |
S297 |