| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163551 | BAA02g10230 | A02 | 4550103 | G | A | synonymous_variant | LOW | c.2184C>T|p.Phe728Phe |
S156 |
| 163552 | BAA02g10230 | A02 | 4551256 | G | A | missense_variant | MODERATE | c.1031C>T|p.Thr344Ile |
S168 |
| 163553 | BAA02g10220 | A02 | 4552644 | C | T | upstream_gene_variant | MODIFIER | c.-2867G>A| |
S18 |
| 163554 | BAA02g10220 | A02 | 4553244 | G | A | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S139 |
| 163555 | BAA02g10220 | A02 | 4553530 | G | A | upstream_gene_variant | MODIFIER | c.-3753C>T| |
S244 |
| 163556 | BAA02g10220 | A02 | 4553970 | C | T | upstream_gene_variant | MODIFIER | c.-4193G>A| |
S135 |
| 163557 | BAA02g10220 | A02 | 4554033 | A | G | upstream_gene_variant | MODIFIER | c.-4256T>C| |
S79 S84 |
| 163558 | BAA02g10220 | A02 | 4554081 | G | A | upstream_gene_variant | MODIFIER | c.-4304C>T| |
S187 |
| 163559 | BAA02g10220 | A02 | 4554628 | C | T | upstream_gene_variant | MODIFIER | c.-4851G>A| |
S30 |
| 163560 | BAA02g10230 | A02 | 4554896 | C | T | upstream_gene_variant | MODIFIER | c.-2530G>A| |
S202 |
| 163561 | BAA02g10230 | A02 | 4555423 | C | T | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S64 |
| 163562 | BAA02g10240 | A02 | 4556067 | C | T | synonymous_variant | LOW | c.21C>T|p.Ile7Ile |
S46 |
| 163563 | BAA02g10240 | A02 | 4556640 | G | A | synonymous_variant | LOW | c.594G>A|p.Lys198Lys |
S159 S243 |
| 163564 | BAA02g10240 | A02 | 4556800 | G | A | missense_variant | MODERATE | c.754G>A|p.Asp252Asn |
S148 S30 S31 |
| 163565 | BAA02g10250 | A02 | 4558688 | G | A | missense_variant | MODERATE | c.41G>A|p.Gly14Glu |
S238 |
| 163566 | BAA02g10240 | A02 | 4560155 | G | A | downstream_gene_variant | MODIFIER | c.*2900G>A| |
S231 |
| 163567 | BAA02g10240 | A02 | 4561935 | C | T | downstream_gene_variant | MODIFIER | c.*4680C>T| |
S243 S250 |
| 163568 | BAA02g10240 | A02 | 4562084 | G | A | downstream_gene_variant | MODIFIER | c.*4829G>A| |
S158 |
| 163569 | BAA02g10260 | A02 | 4562244 | C | T | missense_variant | MODERATE | c.1168G>A|p.Val390Ile |
S288 |
| 163570 | BAA02g10260 | A02 | 4562527 | G | A | synonymous_variant | LOW | c.957C>T|p.Phe319Phe |
S169 |
| 163571 | BAA02g10260 | A02 | 4562862 | C | T | missense_variant | MODERATE | c.622G>A|p.Asp208Asn |
S301 S304 |
| 163572 | BAA02g10250 | A02 | 4563101 | C | T | downstream_gene_variant | MODIFIER | c.*2223C>T| |
S18 |
| 163573 | BAA02g10250 | A02 | 4563123 | G | A | downstream_gene_variant | MODIFIER | c.*2245G>A| |
S206 S26 |
| 163574 | BAA02g10260 | A02 | 4563809 | G | A | synonymous_variant | LOW | c.51C>T|p.Phe17Phe |
S210 |
| 163575 | BAA02g10270 | A02 | 4565473 | C | T | synonymous_variant | LOW | c.1335G>A|p.Gln445Gln |
S83 S88 |