| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158501 | BAA02g06090 | A02 | 2592315 | C | T | synonymous_variant | LOW | c.204C>T|p.Phe68Phe |
S84 S93 |
| 158502 | BAA02g06080 | A02 | 2592829 | C | T | upstream_gene_variant | MODIFIER | c.-3901G>A| |
S138 |
| 158503 | BAA02g06090 | A02 | 2593566 | G | A | missense_variant | MODERATE | c.800G>A|p.Gly267Asp |
S259 |
| 158504 | BAA02g06090 | A02 | 2593842 | C | T | missense_variant | MODERATE | c.905C>T|p.Ala302Val |
S183 S198 |
| 158505 | BAA02g06090 | A02 | 2593866 | C | T | missense_variant | MODERATE | c.929C>T|p.Ser310Leu |
S244 |
| 158506 | BAA02g06090 | A02 | 2593940 | G | A | missense_variant | MODERATE | c.1003G>A|p.Gly335Ser |
S256 |
| 158507 | BAA02g06090 | A02 | 2594200 | G | A | synonymous_variant | LOW | c.1185G>A|p.Gln395Gln |
S210 |
| 158508 | BAA02g06090 | A02 | 2594870 | C | T | missense_variant | MODERATE | c.1360C>T|p.Leu454Phe |
S64 |
| 158509 | BAA02g06100 | A02 | 2596452 | G | A | missense_variant | MODERATE | c.107G>A|p.Gly36Glu |
S174 |
| 158510 | BAA02g06100 | A02 | 2596786 | C | T | missense_variant | MODERATE | c.313C>T|p.Leu105Phe |
S280 |
| 158511 | BAA02g06110 | A02 | 2597068 | C | T | upstream_gene_variant | MODIFIER | c.-2707C>T| |
S42 |
| 158512 | BAA02g06110 | A02 | 2597859 | G | A | upstream_gene_variant | MODIFIER | c.-1916G>A| |
S207 |
| 158513 | BAA02g06110 | A02 | 2599228 | C | T | upstream_gene_variant | MODIFIER | c.-547C>T| |
S15 S153 S181 S2 S213 S217 S248 S3 S4 S6 |
| 158514 | BAA02g06110 | A02 | 2599769 | C | T | upstream_gene_variant | MODIFIER | c.-6C>T| |
S251 |
| 158515 | BAA02g06110 | A02 | 2600294 | G | A | missense_variant | MODERATE | c.520G>A|p.Val174Ile |
S190 |
| 158516 | BAA02g06120 | A02 | 2600724 | G | A | upstream_gene_variant | MODIFIER | c.-1107G>A| |
S283 |
| 158517 | BAA02g06100 | A02 | 2602182 | G | A | downstream_gene_variant | MODIFIER | c.*3543G>A| |
S287 |
| 158518 | BAA02g06120 | A02 | 2602839 | G | A | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S95 |
| 158519 | BAA02g06140 | A02 | 2603028 | G | A | upstream_gene_variant | MODIFIER | c.-4763G>A| |
S169 |
| 158520 | BAA02g06140 | A02 | 2603684 | C | T | upstream_gene_variant | MODIFIER | c.-4107C>T| |
S77 |
| 158521 | BAA02g06140 | A02 | 2603982 | T | C | upstream_gene_variant | MODIFIER | c.-3809T>C| |
S8 |
| 158522 | BAA02g06130 | A02 | 2604812 | G | A | synonymous_variant | LOW | c.1312C>T|p.Leu438Leu |
S297 |
| 158523 | BAA02g06140 | A02 | 2605399 | C | T | upstream_gene_variant | MODIFIER | c.-2392C>T| |
S15 S3 |
| 158524 | BAA02g06130 | A02 | 2607227 | C | T | synonymous_variant | LOW | c.111G>A|p.Val37Val |
S75 S81 |
| 158525 | BAA02g06130 | A02 | 2607692 | G | A | upstream_gene_variant | MODIFIER | c.-355C>T| |
S60 |