| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 86701 | BAA01g46100 | A01 | 30728592 | C | T | downstream_gene_variant | MODIFIER | c.*167C>T| |
S206 S26 |
| 86702 | BAA01g46100 | A01 | 30728902 | C | T | downstream_gene_variant | MODIFIER | c.*477C>T| |
S169 |
| 86703 | BAA01g46100 | A01 | 30729194 | G | A | downstream_gene_variant | MODIFIER | c.*769G>A| |
S189 |
| 86704 | BAA01g46100 | A01 | 30729794 | G | A | downstream_gene_variant | MODIFIER | c.*1369G>A| |
S296 |
| 86705 | BAA01g46100 | A01 | 30730065 | C | T | downstream_gene_variant | MODIFIER | c.*1640C>T| |
S266 |
| 86706 | BAA01g46110 | A01 | 30735406 | G | T | splice_region_variant&intron_variant | LOW | c.110+5G>T| |
S255 |
| 86707 | BAA01g46110 | A01 | 30736361 | G | A | intron_variant | MODIFIER | c.375-142G>A| |
S297 |
| 86708 | BAA01g46110 | A01 | 30736590 | G | A | intron_variant | MODIFIER | c.447+15G>A| |
S139 |
| 86709 | BAA01g46110 | A01 | 30737926 | C | T | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S164 |
| 86710 | BAA01g46110 | A01 | 30739696 | G | A | intron_variant | MODIFIER | c.1139-242G>A| |
S292 |
| 86711 | BAA01g46120 | A01 | 30740570 | C | T | upstream_gene_variant | MODIFIER | c.-4719C>T| |
S107 |
| 86712 | BAA01g46110 | A01 | 30743115 | C | T | missense_variant | MODERATE | c.2521C>T|p.Pro841Ser |
S298 |
| 86713 | BAA01g46120 | A01 | 30743224 | G | A | upstream_gene_variant | MODIFIER | c.-2065G>A| |
S86 |
| 86714 | BAA01g46120 | A01 | 30744449 | G | A | upstream_gene_variant | MODIFIER | c.-840G>A| |
S209 |
| 86715 | BAA01g46120 | A01 | 30744929 | G | A | upstream_gene_variant | MODIFIER | c.-360G>A| |
S157 S163 |
| 86716 | BAA01g46130 | A01 | 30745821 | C | T | upstream_gene_variant | MODIFIER | c.-3213C>T| |
S301 S304 |
| 86717 | BAA01g46130 | A01 | 30746185 | C | T | upstream_gene_variant | MODIFIER | c.-2849C>T| |
S184 |
| 86718 | BAA01g46130 | A01 | 30746336 | G | A | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S124 |
| 86719 | BAA01g46120 | A01 | 30746692 | G | A | missense_variant | MODERATE | c.679G>A|p.Asp227Asn |
S197 |
| 86720 | BAA01g46130 | A01 | 30747194 | C | T | upstream_gene_variant | MODIFIER | c.-1840C>T| |
S274 |
| 86721 | BAA01g46130 | A01 | 30747357 | G | A | upstream_gene_variant | MODIFIER | c.-1677G>A| |
S208 S219 |
| 86722 | BAA01g46130 | A01 | 30748253 | C | T | upstream_gene_variant | MODIFIER | c.-781C>T| |
S192 |
| 86723 | BAA01g46130 | A01 | 30748489 | C | T | upstream_gene_variant | MODIFIER | c.-545C>T| |
S79 S84 |
| 86724 | BAA01g46130 | A01 | 30749894 | G | A | missense_variant | MODERATE | c.296G>A|p.Ser99Asn |
S228 |
| 86725 | BAA01g46130 | A01 | 30750245 | G | A | missense_variant | MODERATE | c.565G>A|p.Asp189Asn |
S67 |