| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156651 | BAA02g04630 | A02 | 2003400 | C | T | missense_variant | MODERATE | c.211G>A|p.Asp71Asn |
S242 |
| 156652 | BAA02g04630 | A02 | 2007317 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S84 S93 |
| 156653 | BAA02g04640 | A02 | 2009222 | G | A | downstream_gene_variant | MODIFIER | c.*1475C>T| |
S107 |
| 156654 | BAA02g04640 | A02 | 2009782 | C | T | downstream_gene_variant | MODIFIER | c.*915G>A| |
S242 |
| 156655 | BAA02g04640 | A02 | 2010351 | C | T | downstream_gene_variant | MODIFIER | c.*346G>A| |
S293 |
| 156656 | BAA02g04640 | A02 | 2010467 | G | A | downstream_gene_variant | MODIFIER | c.*230C>T| |
S76 |
| 156657 | BAA02g04640 | A02 | 2011403 | G | A | missense_variant | MODERATE | c.1691C>T|p.Thr564Ile |
S109 |
| 156658 | BAA02g04640 | A02 | 2011444 | G | A | synonymous_variant | LOW | c.1650C>T|p.Phe550Phe |
S57 |
| 156659 | BAA02g04640 | A02 | 2011640 | G | A | intron_variant | MODIFIER | c.1486-32C>T| |
S45 |
| 156660 | BAA02g04640 | A02 | 2012031 | G | A | missense_variant | MODERATE | c.1442C>T|p.Ala481Val |
S286 |
| 156661 | BAA02g04640 | A02 | 2012716 | C | T | missense_variant | MODERATE | c.833G>A|p.Arg278Lys |
S82 S92 |
| 156662 | BAA02g04640 | A02 | 2014196 | C | T | upstream_gene_variant | MODIFIER | c.-648G>A| |
S180 |
| 156663 | BAA02g04640 | A02 | 2014749 | C | T | upstream_gene_variant | MODIFIER | c.-1201G>A| |
S201 |
| 156664 | BAA02g04640 | A02 | 2014908 | G | A | upstream_gene_variant | MODIFIER | c.-1360C>T| |
S261 |
| 156665 | BAA02g04640 | A02 | 2015446 | C | T | upstream_gene_variant | MODIFIER | c.-1898G>A| |
S100 |
| 156666 | BAA02g04640 | A02 | 2015481 | C | T | upstream_gene_variant | MODIFIER | c.-1933G>A| |
S178 |
| 156667 | BAA02g04640 | A02 | 2015918 | C | T | upstream_gene_variant | MODIFIER | c.-2370G>A| |
S242 |
| 156668 | BAA02g04640 | A02 | 2015942 | G | A | upstream_gene_variant | MODIFIER | c.-2394C>T| |
S5 |
| 156669 | BAA02g04640 | A02 | 2016019 | G | A | upstream_gene_variant | MODIFIER | c.-2471C>T| |
S296 |
| 156670 | BAA02g04640 | A02 | 2016609 | G | A | upstream_gene_variant | MODIFIER | c.-3061C>T| |
S296 |
| 156671 | BAA02g04650 | A02 | 2018214 | G | A | missense_variant | MODERATE | c.80C>T|p.Thr27Ile |
S155 S211 |
| 156672 | BAA02g04640 | A02 | 2018480 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S236 |
| 156673 | BAA02g04640 | A02 | 2018540 | C | T | upstream_gene_variant | MODIFIER | c.-4992G>A| |
S240 |
| 156674 | BAA02g04650 | A02 | 2019156 | G | A | upstream_gene_variant | MODIFIER | c.-863C>T| |
S64 |
| 156675 | BAA02g04650 | A02 | 2021356 | G | A | upstream_gene_variant | MODIFIER | c.-3063C>T| |
S208 |