| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158001 | BAA02g05640 | A02 | 2432670 | C | T | downstream_gene_variant | MODIFIER | c.*3183C>T| |
S38 |
| 158002 | BAA02g05640 | A02 | 2432722 | G | A | downstream_gene_variant | MODIFIER | c.*3235G>A| |
S192 |
| 158003 | BAA02g05640 | A02 | 2433117 | G | C | downstream_gene_variant | MODIFIER | c.*3630G>C| |
S110 |
| 158004 | BAA02g05640 | A02 | 2433917 | C | T | downstream_gene_variant | MODIFIER | c.*4430C>T| |
S167 |
| 158005 | BAA02g05660 | A02 | 2434918 | C | T | upstream_gene_variant | MODIFIER | c.-758G>A| |
S239 |
| 158006 | BAA02g05660 | A02 | 2435561 | G | A | upstream_gene_variant | MODIFIER | c.-1401C>T| |
S150 |
| 158007 | BAA02g05680 | A02 | 2436523 | G | A | missense_variant | MODERATE | c.583C>T|p.Leu195Phe |
S159 |
| 158008 | BAA02g05660 | A02 | 2436873 | G | A | upstream_gene_variant | MODIFIER | c.-2713C>T| |
S190 |
| 158009 | BAA02g05660 | A02 | 2438461 | G | A | upstream_gene_variant | MODIFIER | c.-4301C>T| |
S187 |
| 158010 | BAA02g05660 | A02 | 2438598 | G | A | upstream_gene_variant | MODIFIER | c.-4438C>T| |
S164 S198 |
| 158011 | BAA02g05670 | A02 | 2439779 | C | T | upstream_gene_variant | MODIFIER | c.-4346G>A| |
S104 |
| 158012 | BAA02g05670 | A02 | 2439837 | C | T | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S94 |
| 158013 | BAA02g05670 | A02 | 2440032 | G | A | upstream_gene_variant | MODIFIER | c.-4599C>T| |
S125 |
| 158014 | BAA02g05670 | A02 | 2440092 | G | A | upstream_gene_variant | MODIFIER | c.-4659C>T| |
S155 S211 |
| 158015 | BAA02g05680 | A02 | 2440630 | G | A | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S271 |
| 158016 | BAA02g05680 | A02 | 2440846 | C | T | upstream_gene_variant | MODIFIER | c.-3369G>A| |
S201 |
| 158017 | BAA02g05690 | A02 | 2441843 | C | T | missense_variant | MODERATE | c.418C>T|p.Leu140Phe |
S287 |
| 158018 | BAA02g05690 | A02 | 2442292 | G | A | missense_variant&splice_region_variant | MODERATE | c.712G>A|p.Asp238Asn |
S84 S93 |
| 158019 | BAA02g05690 | A02 | 2442492 | C | T | splice_region_variant&intron_variant | LOW | c.831+6C>T| |
S117 |
| 158020 | BAA02g05710 | A02 | 2442729 | C | T | upstream_gene_variant | MODIFIER | c.-4680C>T| |
S94 |
| 158021 | BAA02g05690 | A02 | 2442876 | G | A | missense_variant | MODERATE | c.1055G>A|p.Gly352Glu |
S98 |
| 158022 | BAA02g05710 | A02 | 2443681 | G | A | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S51 |
| 158023 | BAA02g05710 | A02 | 2443696 | G | A | upstream_gene_variant | MODIFIER | c.-3713G>A| |
S187 |
| 158024 | BAA02g05710 | A02 | 2444143 | C | T | upstream_gene_variant | MODIFIER | c.-3266C>T| |
S79 S84 |
| 158025 | BAA02g05710 | A02 | 2444549 | T | C | upstream_gene_variant | MODIFIER | c.-2860T>C| |
S165 |