Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38750 | A09 | 46487249 | C | T | downstream_gene_variant | MODIFIER | c.*1831G>A| |
S139 |
2 | BAA09g38750 | A09 | 46487656 | C | T | downstream_gene_variant | MODIFIER | c.*1424G>A| |
S247 |
3 | BAA09g38750 | A09 | 46488376 | C | T | downstream_gene_variant | MODIFIER | c.*704G>A| |
S159 S243 S299 |
4 | BAA09g38750 | A09 | 46488393 | G | A | downstream_gene_variant | MODIFIER | c.*687C>T| |
S273 |
5 | BAA09g38750 | A09 | 46488397 | C | T | downstream_gene_variant | MODIFIER | c.*683G>A| |
S94 |
6 | BAA09g38750 | A09 | 46488942 | C | T | downstream_gene_variant | MODIFIER | c.*138G>A| |
S259 |
7 | BAA09g38750 | A09 | 46489424 | C | T | intron_variant | MODIFIER | c.1654-37G>A| |
S13 S278 S279 |
8 | BAA09g38750 | A09 | 46489877 | C | T | synonymous_variant | LOW | c.1251G>A|p.Gln417Gln |
S247 |
9 | BAA09g38750 | A09 | 46490629 | C | T | missense_variant | MODERATE | c.770G>A|p.Arg257Lys |
S54 |
10 | BAA09g38750 | A09 | 46490773 | C | T | missense_variant | MODERATE | c.709G>A|p.Glu237Lys |
S60 |
11 | BAA09g38750 | A09 | 46491719 | C | T | intron_variant | MODIFIER | c.330+68G>A| |
S135 |
12 | BAA09g38750 | A09 | 46491864 | G | A | stop_gained | HIGH | c.253C>T|p.Arg85* |
S116 |
13 | BAA09g38750 | A09 | 46492003 | C | T | missense_variant | MODERATE | c.214G>A|p.Glu72Lys |
S293 |
14 | BAA09g38750 | A09 | 46493423 | G | A | upstream_gene_variant | MODIFIER | c.-1207C>T| |
S105 S106 |
15 | BAA09g38750 | A09 | 46494223 | G | A | upstream_gene_variant | MODIFIER | c.-2007C>T| |
S188 |
16 | BAA09g38750 | A09 | 46494546 | G | A | upstream_gene_variant | MODIFIER | c.-2330C>T| |
S7 |
17 | BAA09g38750 | A09 | 46495364 | T | C | upstream_gene_variant | MODIFIER | c.-3148A>G| |
S262 |
18 | BAA09g38750 | A09 | 46496033 | G | A | upstream_gene_variant | MODIFIER | c.-3817C>T| |
S290 |
19 | BAA09g38750 | A09 | 46496429 | C | T | upstream_gene_variant | MODIFIER | c.-4213G>A| |
S66 |
20 | BAA09g38750 | A09 | 46496889 | G | A | upstream_gene_variant | MODIFIER | c.-4673C>T| |
S271 |