| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155901 | BAA02g04010 | A02 | 1736430 | G | A | synonymous_variant | LOW | c.57G>A|p.Gln19Gln |
S131 |
| 155902 | BAA02g04020 | A02 | 1740794 | G | A | upstream_gene_variant | MODIFIER | c.-1328C>T| |
S305 |
| 155903 | BAA02g04020 | A02 | 1741458 | G | A | upstream_gene_variant | MODIFIER | c.-1992C>T| |
S308 |
| 155904 | BAA02g04020 | A02 | 1741535 | C | T | upstream_gene_variant | MODIFIER | c.-2069G>A| |
S116 |
| 155905 | BAA02g04020 | A02 | 1742684 | G | A | upstream_gene_variant | MODIFIER | c.-3218C>T| |
S86 |
| 155906 | BAA02g04020 | A02 | 1743253 | G | A | upstream_gene_variant | MODIFIER | c.-3787C>T| |
S13 |
| 155907 | BAA02g04020 | A02 | 1744086 | C | T | upstream_gene_variant | MODIFIER | c.-4620G>A| |
S108 |
| 155908 | BAA02g04030 | A02 | 1746508 | C | T | synonymous_variant | LOW | c.9C>T|p.Phe3Phe |
S292 |
| 155909 | BAA02g04030 | A02 | 1747032 | G | A | missense_variant | MODERATE | c.533G>A|p.Gly178Glu |
S208 |
| 155910 | BAA02g04040 | A02 | 1748084 | C | T | downstream_gene_variant | MODIFIER | c.*3717G>A| |
S46 |
| 155911 | BAA02g04030 | A02 | 1748559 | G | A | missense_variant | MODERATE | c.1045G>A|p.Gly349Arg |
S25 |
| 155912 | BAA02g04030 | A02 | 1750336 | C | T | downstream_gene_variant | MODIFIER | c.*1415C>T| |
S207 |
| 155913 | BAA02g04030 | A02 | 1751068 | G | A | downstream_gene_variant | MODIFIER | c.*2147G>A| |
S63 |
| 155914 | BAA02g04050 | A02 | 1751446 | C | T | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S79 S84 |
| 155915 | BAA02g04040 | A02 | 1751848 | G | A | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S59 |
| 155916 | BAA02g04040 | A02 | 1752198 | C | T | missense_variant | MODERATE | c.44G>A|p.Arg15Lys |
S115 |
| 155917 | BAA02g04040 | A02 | 1752367 | G | A | upstream_gene_variant | MODIFIER | c.-126C>T| |
S269 |
| 155918 | BAA02g04040 | A02 | 1752456 | C | T | upstream_gene_variant | MODIFIER | c.-215G>A| |
S289 S290 |
| 155919 | BAA02g04040 | A02 | 1752927 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S198 |
| 155920 | BAA02g04040 | A02 | 1752934 | G | A | upstream_gene_variant | MODIFIER | c.-693C>T| |
S210 S225 |
| 155921 | BAA02g04040 | A02 | 1755417 | G | A | upstream_gene_variant | MODIFIER | c.-3176C>T| |
S11 |
| 155922 | BAA02g04050 | A02 | 1756307 | C | T | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S15 S3 |
| 155923 | BAA02g04040 | A02 | 1756765 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S209 |
| 155924 | BAA02g04040 | A02 | 1757044 | G | A | upstream_gene_variant | MODIFIER | c.-4803C>T| |
S110 |
| 155925 | BAA02g04050 | A02 | 1757465 | G | A | downstream_gene_variant | MODIFIER | c.*761G>A| |
S45 |