| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170801 | BAA02g15280 | A02 | 7328621 | C | T | downstream_gene_variant | MODIFIER | c.*323G>A| |
S186 |
| 170802 | BAA02g15280 | A02 | 7328762 | G | A | downstream_gene_variant | MODIFIER | c.*182C>T| |
S295 |
| 170803 | BAA02g15280 | A02 | 7329347 | C | T | missense_variant | MODERATE | c.3314G>A|p.Arg1105Lys |
S205 |
| 170804 | BAA02g15280 | A02 | 7329749 | G | A | missense_variant | MODERATE | c.2912C>T|p.Ala971Val |
S204 |
| 170805 | BAA02g15280 | A02 | 7329774 | G | A | missense_variant | MODERATE | c.2887C>T|p.His963Tyr |
S279 |
| 170806 | BAA02g15280 | A02 | 7330086 | G | A | missense_variant | MODERATE | c.2575C>T|p.His859Tyr |
S47 |
| 170807 | BAA02g15280 | A02 | 7330996 | G | A | intron_variant | MODIFIER | c.2352-687C>T| |
S41 |
| 170808 | BAA02g15280 | A02 | 7331139 | G | A | intron_variant | MODIFIER | c.2351+647C>T| |
S109 |
| 170809 | BAA02g15280 | A02 | 7331339 | G | A | intron_variant | MODIFIER | c.2351+447C>T| |
S105 |
| 170810 | BAA02g15280 | A02 | 7331340 | C | T | intron_variant | MODIFIER | c.2351+446G>A| |
S9 |
| 170811 | BAA02g15280 | A02 | 7331576 | G | A | intron_variant | MODIFIER | c.2351+210C>T| |
S265 |
| 170812 | BAA02g15280 | A02 | 7331649 | T | C | intron_variant | MODIFIER | c.2351+137A>G| |
S32 |
| 170813 | BAA02g15280 | A02 | 7331755 | G | A | intron_variant | MODIFIER | c.2351+31C>T| |
S45 |
| 170814 | BAA02g15280 | A02 | 7331802 | C | T | missense_variant | MODERATE | c.2335G>A|p.Glu779Lys |
S88 |
| 170815 | BAA02g15280 | A02 | 7331996 | C | T | missense_variant | MODERATE | c.2141G>A|p.Arg714Lys |
S242 |
| 170816 | BAA02g15280 | A02 | 7332011 | C | T | missense_variant | MODERATE | c.2126G>A|p.Gly709Glu |
S273 |
| 170817 | BAA02g15280 | A02 | 7332035 | C | T | missense_variant | MODERATE | c.2102G>A|p.Ser701Asn |
S123 S278 |
| 170818 | BAA02g15280 | A02 | 7332390 | G | A | intron_variant | MODIFIER | c.1828-81C>T| |
S45 |
| 170819 | BAA02g15280 | A02 | 7332522 | C | T | intron_variant | MODIFIER | c.1828-213G>A| |
S25 |
| 170820 | BAA02g15280 | A02 | 7332560 | G | T | intron_variant | MODIFIER | c.1828-251C>A| |
S71 |
| 170821 | BAA02g15280 | A02 | 7333126 | G | A | missense_variant | MODERATE | c.1805C>T|p.Ala602Val |
S64 |
| 170822 | BAA02g15280 | A02 | 7333486 | C | T | missense_variant | MODERATE | c.1445G>A|p.Gly482Glu |
S25 |
| 170823 | BAA02g15280 | A02 | 7333557 | G | A | synonymous_variant | LOW | c.1374C>T|p.Pro458Pro |
S282 |
| 170824 | BAA02g15280 | A02 | 7333810 | C | T | missense_variant | MODERATE | c.1121G>A|p.Gly374Glu |
S221 |
| 170825 | BAA02g15280 | A02 | 7333964 | G | A | stop_gained | HIGH | c.967C>T|p.Gln323* |
S228 |