| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g33970 | A05 | 35407169 | C | T | intron_variant | MODIFIER | c.3064+951G>A| |
S176 |
| 2 | BAA05g33970 | A05 | 35407204 | C | T | intron_variant | MODIFIER | c.3064+916G>A| |
S162 |
| 3 | BAA05g33970 | A05 | 35407635 | G | A | intron_variant | MODIFIER | c.3064+485C>T| |
S205 |
| 4 | BAA05g33970 | A05 | 35408129 | C | T | missense_variant | MODERATE | c.3055G>A|p.Glu1019Lys |
S83 S88 |
| 5 | BAA05g33970 | A05 | 35408507 | G | A | missense_variant | MODERATE | c.2677C>T|p.Pro893Ser |
S34 |
| 6 | BAA05g33970 | A05 | 35408680 | G | A | missense_variant | MODERATE | c.2504C>T|p.Ser835Phe |
S150 |
| 7 | BAA05g33970 | A05 | 35409087 | C | T | synonymous_variant | LOW | c.2097G>A|p.Pro699Pro |
S270 |
| 8 | BAA05g33970 | A05 | 35409795 | G | A | missense_variant | MODERATE | c.1487C>T|p.Ser496Phe |
S275 |
| 9 | BAA05g33970 | A05 | 35410040 | C | T | synonymous_variant | LOW | c.1242G>A|p.Lys414Lys |
S99 |
| 10 | BAA05g33970 | A05 | 35411537 | G | A | upstream_gene_variant | MODIFIER | c.-256C>T| |
S231 |
| 11 | BAA05g33970 | A05 | 35411731 | C | T | upstream_gene_variant | MODIFIER | c.-450G>A| |
S162 |
| 12 | BAA05g33970 | A05 | 35411963 | C | T | upstream_gene_variant | MODIFIER | c.-682G>A| |
S295 |
| 13 | BAA05g33970 | A05 | 35412894 | G | A | upstream_gene_variant | MODIFIER | c.-1613C>T| |
S276 |
| 14 | BAA05g33970 | A05 | 35413200 | G | A | upstream_gene_variant | MODIFIER | c.-1919C>T| |
S90 |
| 15 | BAA05g33970 | A05 | 35413311 | C | T | upstream_gene_variant | MODIFIER | c.-2030G>A| |
S67 |