Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33460 | A09 | 42034999 | C | T | downstream_gene_variant | MODIFIER | c.*3524G>A| |
S120 |
2 | BAA09g33460 | A09 | 42035394 | G | A | downstream_gene_variant | MODIFIER | c.*3129C>T| |
S11 |
3 | BAA09g33460 | A09 | 42035907 | G | A | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S200 |
4 | BAA09g33460 | A09 | 42036138 | C | T | downstream_gene_variant | MODIFIER | c.*2385G>A| |
S30 S31 |
5 | BAA09g33460 | A09 | 42036309 | C | T | downstream_gene_variant | MODIFIER | c.*2214G>A| |
S192 |
6 | BAA09g33460 | A09 | 42036748 | C | T | downstream_gene_variant | MODIFIER | c.*1775G>A| |
S246 |
7 | BAA09g33460 | A09 | 42036970 | G | A | downstream_gene_variant | MODIFIER | c.*1553C>T| |
S223 |
8 | BAA09g33460 | A09 | 42037538 | T | A | downstream_gene_variant | MODIFIER | c.*985A>T| |
S125 S162 |
9 | BAA09g33460 | A09 | 42037697 | G | A | downstream_gene_variant | MODIFIER | c.*826C>T| |
S78 S83 |
10 | BAA09g33460 | A09 | 42037813 | G | A | downstream_gene_variant | MODIFIER | c.*710C>T| |
S271 |
11 | BAA09g33460 | A09 | 42038960 | C | T | missense_variant | MODERATE | c.1882G>A|p.Gly628Ser |
S237 |
12 | BAA09g33460 | A09 | 42039473 | G | A | synonymous_variant | LOW | c.1549C>T|p.Leu517Leu |
S33 |
13 | BAA09g33460 | A09 | 42039814 | C | T | missense_variant | MODERATE | c.1345G>A|p.Gly449Arg |
S211 S227 |
14 | BAA09g33460 | A09 | 42041517 | C | T | missense_variant | MODERATE | c.97G>A|p.Gly33Ser |
S159 S243 S299 |
15 | BAA09g33460 | A09 | 42043660 | C | T | upstream_gene_variant | MODIFIER | c.-1962G>A| |
S259 |
16 | BAA09g33460 | A09 | 42045475 | G | A | upstream_gene_variant | MODIFIER | c.-3777C>T| |
S196 |
17 | BAA09g33460 | A09 | 42045517 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S40 S49 |