Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39390 | A09 | 47021319 | G | A | stop_gained | HIGH | c.2230C>T|p.Gln744* |
S38 |
2 | BAA09g39390 | A09 | 47021350 | G | A | synonymous_variant | LOW | c.2199C>T|p.Ile733Ile |
S289 S290 |
3 | BAA09g39390 | A09 | 47021810 | C | T | missense_variant | MODERATE | c.1817G>A|p.Gly606Asp |
S191 |
4 | BAA09g39390 | A09 | 47022080 | G | A | missense_variant | MODERATE | c.1706C>T|p.Pro569Leu |
S201 |
5 | BAA09g39390 | A09 | 47022251 | G | A | missense_variant | MODERATE | c.1622C>T|p.Ala541Val |
S288 |
6 | BAA09g39390 | A09 | 47023034 | C | T | synonymous_variant | LOW | c.1077G>A|p.Lys359Lys |
S179 |
7 | BAA09g39390 | A09 | 47027381 | G | A | upstream_gene_variant | MODIFIER | c.-3271C>T| |
S162 |
8 | BAA09g39390 | A09 | 47027699 | C | T | upstream_gene_variant | MODIFIER | c.-3589G>A| |
S80 |
9 | BAA09g39390 | A09 | 47027774 | C | T | upstream_gene_variant | MODIFIER | c.-3664G>A| |
S43 |
10 | BAA09g39390 | A09 | 47028045 | C | T | upstream_gene_variant | MODIFIER | c.-3935G>A| |
S293 |
11 | BAA09g39390 | A09 | 47028054 | C | T | upstream_gene_variant | MODIFIER | c.-3944G>A| |
S5 |
12 | BAA09g39390 | A09 | 47028455 | G | A | upstream_gene_variant | MODIFIER | c.-4345C>T| |
S172 S217 |
13 | BAA09g39390 | A09 | 47028738 | C | T | upstream_gene_variant | MODIFIER | c.-4628G>A| |
S56 S67 |
14 | BAA09g39390 | A09 | 47028841 | C | T | upstream_gene_variant | MODIFIER | c.-4731G>A| |
S295 |
15 | BAA09g39390 | A09 | 47028853 | G | A | upstream_gene_variant | MODIFIER | c.-4743C>T| |
S249 |
16 | BAA09g39390 | A09 | 47028854 | G | A | upstream_gene_variant | MODIFIER | c.-4744C>T| |
S151 S263 |