| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 180751 | BAA02g20500 | A02 | 10882603 | G | A | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S91 |
| 180752 | BAA02g20500 | A02 | 10882636 | G | A | synonymous_variant | LOW | c.40C>T|p.Leu14Leu |
S200 |
| 180753 | BAA02g20500 | A02 | 10883452 | G | A | upstream_gene_variant | MODIFIER | c.-777C>T| |
S69 |
| 180754 | BAA02g20500 | A02 | 10884490 | C | T | upstream_gene_variant | MODIFIER | c.-1815G>A| |
S108 |
| 180755 | BAA02g20510 | A02 | 10884885 | C | T | missense_variant | MODERATE | c.1589G>A|p.Arg530Lys |
S32 |
| 180756 | BAA02g20510 | A02 | 10885830 | G | A | missense_variant | MODERATE | c.644C>T|p.Pro215Leu |
S4 |
| 180757 | BAA02g20510 | A02 | 10886112 | C | T | missense_variant | MODERATE | c.362G>A|p.Arg121His |
S283 |
| 180758 | BAA02g20500 | A02 | 10886611 | G | A | upstream_gene_variant | MODIFIER | c.-3936C>T| |
S155 S211 |
| 180759 | BAA02g20500 | A02 | 10886648 | C | T | upstream_gene_variant | MODIFIER | c.-3973G>A| |
S40 S49 |
| 180760 | BAA02g20500 | A02 | 10887190 | G | A | upstream_gene_variant | MODIFIER | c.-4515C>T| |
S210 |
| 180761 | BAA02g20500 | A02 | 10887414 | G | A | upstream_gene_variant | MODIFIER | c.-4739C>T| |
S148 S30 S31 |
| 180762 | BAA02g20520 | A02 | 10888615 | C | T | missense_variant | MODERATE | c.328G>A|p.Val110Met |
S218 |
| 180763 | BAA02g20510 | A02 | 10889783 | G | A | upstream_gene_variant | MODIFIER | c.-3310C>T| |
S256 |
| 180764 | BAA02g20510 | A02 | 10889826 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S263 |
| 180765 | BAA02g20510 | A02 | 10889852 | C | T | upstream_gene_variant | MODIFIER | c.-3379G>A| |
S234 |
| 180766 | BAA02g20510 | A02 | 10890039 | G | A | upstream_gene_variant | MODIFIER | c.-3566C>T| |
S296 |
| 180767 | BAA02g20510 | A02 | 10890164 | C | T | upstream_gene_variant | MODIFIER | c.-3691G>A| |
S219 S72 |
| 180768 | BAA02g20510 | A02 | 10890374 | G | A | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S44 |
| 180769 | BAA02g20510 | A02 | 10890718 | C | T | upstream_gene_variant | MODIFIER | c.-4245G>A| |
S171 |
| 180770 | BAA02g20510 | A02 | 10890741 | C | T | upstream_gene_variant | MODIFIER | c.-4268G>A| |
S268 |
| 180771 | BAA02g20510 | A02 | 10890831 | C | T | upstream_gene_variant | MODIFIER | c.-4358G>A| |
S84 |
| 180772 | BAA02g20520 | A02 | 10891515 | T | A | upstream_gene_variant | MODIFIER | c.-2225A>T| |
S142 S164 S177 S206 S208 S217 S219 S230 S26 S63 S72 |
| 180773 | BAA02g20520 | A02 | 10892716 | C | T | upstream_gene_variant | MODIFIER | c.-3426G>A| |
S216 |
| 180774 | BAA02g20530 | A02 | 10894410 | C | T | intron_variant | MODIFIER | c.390-72G>A| |
S112 |
| 180775 | BAA02g20530 | A02 | 10895207 | G | A | synonymous_variant | LOW | c.318C>T|p.Pro106Pro |
S200 |