Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36250 | A09 | 44613050 | C | T | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S36 |
2 | BAA09g36250 | A09 | 44613163 | C | T | upstream_gene_variant | MODIFIER | c.-4413C>T| |
S109 |
3 | BAA09g36250 | A09 | 44613751 | C | T | upstream_gene_variant | MODIFIER | c.-3825C>T| |
S246 |
4 | BAA09g36250 | A09 | 44614223 | G | A | upstream_gene_variant | MODIFIER | c.-3353G>A| |
S200 |
5 | BAA09g36250 | A09 | 44614536 | C | T | upstream_gene_variant | MODIFIER | c.-3040C>T| |
S202 |
6 | BAA09g36250 | A09 | 44614919 | C | T | upstream_gene_variant | MODIFIER | c.-2657C>T| |
S135 |
7 | BAA09g36250 | A09 | 44615352 | G | A | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S177 |
8 | BAA09g36250 | A09 | 44616437 | G | A | upstream_gene_variant | MODIFIER | c.-1139G>A| |
S176 |
9 | BAA09g36250 | A09 | 44616504 | G | A | upstream_gene_variant | MODIFIER | c.-1072G>A| |
S262 |
10 | BAA09g36250 | A09 | 44616514 | G | A | upstream_gene_variant | MODIFIER | c.-1062G>A| |
S64 |
11 | BAA09g36250 | A09 | 44616578 | C | T | upstream_gene_variant | MODIFIER | c.-998C>T| |
S174 S27 |
12 | BAA09g36250 | A09 | 44616612 | C | T | upstream_gene_variant | MODIFIER | c.-964C>T| |
S155 S211 |
13 | BAA09g36250 | A09 | 44616863 | G | A | upstream_gene_variant | MODIFIER | c.-713G>A| |
S17 |
14 | BAA09g36250 | A09 | 44617104 | C | T | upstream_gene_variant | MODIFIER | c.-472C>T| |
S18 |
15 | BAA09g36250 | A09 | 44617186 | G | A | upstream_gene_variant | MODIFIER | c.-390G>A| |
S225 S73 |
16 | BAA09g36250 | A09 | 44617654 | C | T | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S186 |
17 | BAA09g36250 | A09 | 44617895 | C | T | intron_variant | MODIFIER | c.112-134C>T| |
S159 S243 S299 |
18 | BAA09g36250 | A09 | 44618842 | C | T | missense_variant | MODERATE | c.626C>T|p.Ala209Val |
S257 |
19 | BAA09g36250 | A09 | 44619433 | C | T | downstream_gene_variant | MODIFIER | c.*551C>T| |
S269 |
20 | BAA09g36250 | A09 | 44623742 | C | T | downstream_gene_variant | MODIFIER | c.*4860C>T| |
S132 S137 S215 |
21 | BAA09g36250 | A09 | 44623849 | G | A | downstream_gene_variant | MODIFIER | c.*4967G>A| |
S176 |