Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07170 | A09 | 3995634 | G | A | downstream_gene_variant | MODIFIER | c.*4688C>T| |
S126 |
2 | BAA09g07170 | A09 | 3996199 | G | A | downstream_gene_variant | MODIFIER | c.*4123C>T| |
S240 |
3 | BAA09g07170 | A09 | 3996345 | G | T | downstream_gene_variant | MODIFIER | c.*3977C>A| |
S138 S174 S175 S204 S256 S277 S296 S3 S305 S36 S38 S59 S6 S61 S73 S91 |
4 | BAA09g07170 | A09 | 3996455 | T | A | downstream_gene_variant | MODIFIER | c.*3867A>T| |
S227 S276 S284 S287 S43 S56 S7 |
5 | BAA09g07170 | A09 | 3996852 | C | T | downstream_gene_variant | MODIFIER | c.*3470G>A| |
S170 S191 S203 S212 S213 S215 S240 S71 S88 S9 |
6 | BAA09g07170 | A09 | 3997882 | G | A | downstream_gene_variant | MODIFIER | c.*2440C>T| |
S296 |
7 | BAA09g07170 | A09 | 3998061 | G | A | downstream_gene_variant | MODIFIER | c.*2261C>T| |
S38 |
8 | BAA09g07170 | A09 | 3999345 | G | A | downstream_gene_variant | MODIFIER | c.*977C>T| |
S161 |
9 | BAA09g07170 | A09 | 4000462 | C | T | missense_variant | MODERATE | c.628G>A|p.Gly210Ser |
S8 |
10 | BAA09g07170 | A09 | 4000498 | C | T | missense_variant | MODERATE | c.592G>A|p.Ala198Thr |
S277 |
11 | BAA09g07170 | A09 | 4000977 | G | A | missense_variant | MODERATE | c.113C>T|p.Pro38Leu |
S291 |
12 | BAA09g07170 | A09 | 4001057 | G | A | synonymous_variant | LOW | c.33C>T|p.Ser11Ser |
S95 |
13 | BAA09g07170 | A09 | 4001654 | G | A | upstream_gene_variant | MODIFIER | c.-565C>T| |
S245 |
14 | BAA09g07170 | A09 | 4003338 | C | T | upstream_gene_variant | MODIFIER | c.-2249G>A| |
S213 |
15 | BAA09g07170 | A09 | 4003543 | G | A | upstream_gene_variant | MODIFIER | c.-2454C>T| |
S139 |
16 | BAA09g07170 | A09 | 4003770 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S150 |
17 | BAA09g07170 | A09 | 4005112 | G | A | upstream_gene_variant | MODIFIER | c.-4023C>T| |
S95 |