| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 62801 | BAA01g33110-BAA01g33120 | A01 | 22023414 | G | A | intergenic_region | MODIFIER | n.22023414G>A| |
S33 |
| 62802 | BAA01g33110-BAA01g33120 | A01 | 22024482 | G | A | intergenic_region | MODIFIER | n.22024482G>A| |
S37 |
| 62803 | BAA01g33120 | A01 | 22025557 | G | A | upstream_gene_variant | MODIFIER | c.-4618G>A| |
S42 |
| 62804 | BAA01g33120 | A01 | 22025612 | G | A | upstream_gene_variant | MODIFIER | c.-4563G>A| |
S221 |
| 62805 | BAA01g33120 | A01 | 22026974 | C | T | upstream_gene_variant | MODIFIER | c.-3201C>T| |
S19 |
| 62806 | BAA01g33120 | A01 | 22027869 | C | T | upstream_gene_variant | MODIFIER | c.-2306C>T| |
S193 |
| 62807 | BAA01g33120 | A01 | 22030748 | G | A | missense_variant | MODERATE | c.121G>A|p.Gly41Arg |
S62 |
| 62808 | BAA01g33120 | A01 | 22030969 | C | T | missense_variant | MODERATE | c.245C>T|p.Ala82Val |
S167 |
| 62809 | BAA01g33130 | A01 | 22031151 | C | T | downstream_gene_variant | MODIFIER | c.*2251G>A| |
S113 |
| 62810 | BAA01g33120 | A01 | 22031721 | C | T | missense_variant | MODERATE | c.500C>T|p.Thr167Ile |
S267 |
| 62811 | BAA01g33140 | A01 | 22032227 | C | T | upstream_gene_variant | MODIFIER | c.-4082C>T| |
S11 |
| 62812 | BAA01g33120 | A01 | 22032503 | C | T | synonymous_variant | LOW | c.858C>T|p.Asp286Asp |
S192 |
| 62813 | BAA01g33140 | A01 | 22033092 | C | A | upstream_gene_variant | MODIFIER | c.-3217C>A| |
S245 |
| 62814 | BAA01g33140 | A01 | 22033385 | G | A | upstream_gene_variant | MODIFIER | c.-2924G>A| |
S6 |
| 62815 | BAA01g33130 | A01 | 22033450 | G | A | synonymous_variant | LOW | c.609C>T|p.Leu203Leu |
S217 S248 |
| 62816 | BAA01g33140 | A01 | 22034144 | C | T | upstream_gene_variant | MODIFIER | c.-2165C>T| |
S9 |
| 62817 | BAA01g33130 | A01 | 22035153 | G | A | upstream_gene_variant | MODIFIER | c.-651C>T| |
S176 |
| 62818 | BAA01g33130 | A01 | 22035744 | C | T | upstream_gene_variant | MODIFIER | c.-1242G>A| |
S111 |
| 62819 | BAA01g33130 | A01 | 22035789 | C | T | upstream_gene_variant | MODIFIER | c.-1287G>A| |
S46 |
| 62820 | BAA01g33140 | A01 | 22036393 | C | T | missense_variant | MODERATE | c.85C>T|p.Leu29Phe |
S139 |
| 62821 | BAA01g33140 | A01 | 22036864 | C | T | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S142 |
| 62822 | BAA01g33140 | A01 | 22036875 | G | A | missense_variant | MODERATE | c.454G>A|p.Ala152Thr |
S163 |
| 62823 | BAA01g33130 | A01 | 22037614 | C | T | upstream_gene_variant | MODIFIER | c.-3112G>A| |
S182 |
| 62824 | BAA01g33140 | A01 | 22039696 | G | A | downstream_gene_variant | MODIFIER | c.*2783G>A| |
S15 S3 |
| 62825 | BAA01g33140 | A01 | 22039904 | C | T | downstream_gene_variant | MODIFIER | c.*2991C>T| |
S94 |