| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11951 | BAA01g09570 | A01 | 4260440 | C | T | intron_variant | MODIFIER | c.736-183G>A| |
S247 |
| 11952 | BAA01g09570 | A01 | 4260562 | G | A | intron_variant | MODIFIER | c.735+94C>T| |
S181 |
| 11953 | BAA01g09570 | A01 | 4260819 | G | A | missense_variant | MODERATE | c.649C>T|p.Leu217Phe |
S96 |
| 11954 | BAA01g09580 | A01 | 4260912 | C | T | downstream_gene_variant | MODIFIER | c.*4902G>A| |
S53 |
| 11955 | BAA01g09570 | A01 | 4261635 | G | A | missense_variant | MODERATE | c.25C>T|p.Pro9Ser |
S207 |
| 11956 | BAA01g09570 | A01 | 4261892 | C | T | upstream_gene_variant | MODIFIER | c.-233G>A| |
S109 |
| 11957 | BAA01g09570 | A01 | 4262964 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S97 |
| 11958 | BAA01g09570 | A01 | 4263550 | G | A | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S280 |
| 11959 | BAA01g09570 | A01 | 4263807 | C | T | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S155 S211 |
| 11960 | BAA01g09570 | A01 | 4264167 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S192 |
| 11961 | BAA01g09580 | A01 | 4266322 | C | T | missense_variant | MODERATE | c.782G>A|p.Gly261Asp |
S53 |
| 11962 | BAA01g09570 | A01 | 4266569 | C | T | upstream_gene_variant | MODIFIER | c.-4910G>A| |
S246 |
| 11963 | BAA01g09590 | A01 | 4267571 | G | A | upstream_gene_variant | MODIFIER | c.-3194G>A| |
S105 S106 |
| 11964 | BAA01g09580 | A01 | 4269234 | C | T | upstream_gene_variant | MODIFIER | c.-1081G>A| |
S296 |
| 11965 | BAA01g09580 | A01 | 4269642 | G | A | upstream_gene_variant | MODIFIER | c.-1489C>T| |
S162 |
| 11966 | BAA01g09580 | A01 | 4269661 | G | A | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S167 |
| 11967 | BAA01g09580 | A01 | 4269693 | C | T | upstream_gene_variant | MODIFIER | c.-1540G>A| |
S249 |
| 11968 | BAA01g09580 | A01 | 4270682 | C | T | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S270 |
| 11969 | BAA01g09590 | A01 | 4270937 | C | T | missense_variant | MODERATE | c.173C>T|p.Pro58Leu |
S61 |
| 11970 | BAA01g09590 | A01 | 4271006 | C | T | missense_variant | MODERATE | c.242C>T|p.Pro81Leu |
S166 |
| 11971 | BAA01g09590 | A01 | 4271033 | G | A | missense_variant | MODERATE | c.269G>A|p.Gly90Asp |
S74 |
| 11972 | BAA01g09590 | A01 | 4272153 | G | A | synonymous_variant | LOW | c.801G>A|p.Gln267Gln |
S228 |
| 11973 | BAA01g09600 | A01 | 4273863 | C | T | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S265 |
| 11974 | BAA01g09600 | A01 | 4274148 | C | T | missense_variant | MODERATE | c.1021G>A|p.Val341Met |
S242 |
| 11975 | BAA01g09600 | A01 | 4274260 | C | T | synonymous_variant | LOW | c.909G>A|p.Leu303Leu |
S133 |