Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g06210 | A09 | 3457993 | G | A | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S139 S271 |
2 | BAA09g06210 | A09 | 3458319 | G | A | upstream_gene_variant | MODIFIER | c.-4458G>A| |
S33 |
3 | BAA09g06210 | A09 | 3459493 | G | A | upstream_gene_variant | MODIFIER | c.-3284G>A| |
S280 |
4 | BAA09g06210 | A09 | 3460427 | G | A | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S205 |
5 | BAA09g06210 | A09 | 3462579 | C | T | upstream_gene_variant | MODIFIER | c.-198C>T| |
S270 |
6 | BAA09g06210 | A09 | 3462775 | G | A | upstream_gene_variant | MODIFIER | c.-2G>A| |
S185 |
7 | BAA09g06210 | A09 | 3462943 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Leu |
S293 |
8 | BAA09g06210 | A09 | 3463616 | G | A | synonymous_variant | LOW | c.762G>A|p.Glu254Glu |
S152 |
9 | BAA09g06210 | A09 | 3463922 | C | T | missense_variant | MODERATE | c.989C>T|p.Ala330Val |
S261 |
10 | BAA09g06210 | A09 | 3464189 | C | T | intron_variant | MODIFIER | c.1182+74C>T| |
S230 |
11 | BAA09g06210 | A09 | 3465250 | G | A | synonymous_variant | LOW | c.1752G>A|p.Gln584Gln |
S30 S31 |
12 | BAA09g06210 | A09 | 3466630 | G | A | downstream_gene_variant | MODIFIER | c.*1281G>A| |
S299 |
13 | BAA09g06210 | A09 | 3466748 | G | A | downstream_gene_variant | MODIFIER | c.*1399G>A| |
S69 |
14 | BAA09g06210 | A09 | 3467135 | C | T | downstream_gene_variant | MODIFIER | c.*1786C>T| |
S168 S85 |
15 | BAA09g06210 | A09 | 3468406 | C | T | downstream_gene_variant | MODIFIER | c.*3057C>T| |
S119 S246 |
16 | BAA09g06210 | A09 | 3468793 | C | T | downstream_gene_variant | MODIFIER | c.*3444C>T| |
S143 |