Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16290 | A09 | 9466998 | C | T | downstream_gene_variant | MODIFIER | c.*4936G>A| |
S263 S297 |
2 | BAA09g16290 | A09 | 9468415 | G | A | downstream_gene_variant | MODIFIER | c.*3519C>T| |
S223 |
3 | BAA09g16290 | A09 | 9468444 | G | A | downstream_gene_variant | MODIFIER | c.*3490C>T| |
S74 |
4 | BAA09g16290 | A09 | 9472019 | C | T | missense_variant | MODERATE | c.2150G>A|p.Arg717Lys |
S131 |
5 | BAA09g16290 | A09 | 9472485 | G | A | missense_variant | MODERATE | c.1684C>T|p.Pro562Ser |
S88 |
6 | BAA09g16290 | A09 | 9472788 | G | A | stop_gained | HIGH | c.1381C>T|p.Gln461* |
S244 |
7 | BAA09g16290 | A09 | 9472913 | G | A | missense_variant | MODERATE | c.1256C>T|p.Pro419Leu |
S75 |
8 | BAA09g16290 | A09 | 9473210 | G | A | missense_variant | MODERATE | c.1034C>T|p.Pro345Leu |
S271 |
9 | BAA09g16290 | A09 | 9473635 | C | T | synonymous_variant | LOW | c.609G>A|p.Gln203Gln |
S107 |
10 | BAA09g16290 | A09 | 9473829 | G | A | missense_variant | MODERATE | c.415C>T|p.His139Tyr |
S88 |
11 | BAA09g16290 | A09 | 9473881 | C | T | synonymous_variant | LOW | c.363G>A|p.Ala121Ala |
S234 |
12 | BAA09g16290 | A09 | 9474096 | C | T | missense_variant | MODERATE | c.148G>A|p.Ala50Thr |
S140 |
13 | BAA09g16290 | A09 | 9474944 | G | A | upstream_gene_variant | MODIFIER | c.-701C>T| |
S190 |
14 | BAA09g16290 | A09 | 9475007 | G | A | upstream_gene_variant | MODIFIER | c.-764C>T| |
S46 |
15 | BAA09g16290 | A09 | 9476420 | C | T | upstream_gene_variant | MODIFIER | c.-2177G>A| |
S295 |
16 | BAA09g16290 | A09 | 9477994 | C | T | upstream_gene_variant | MODIFIER | c.-3751G>A| |
S256 |
17 | BAA09g16290 | A09 | 9478199 | G | A | upstream_gene_variant | MODIFIER | c.-3956C>T| |
S252 |