| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157551 | BAA02g05240 | A02 | 2296794 | C | T | synonymous_variant | LOW | c.168G>A|p.Arg56Arg |
S242 |
| 157552 | BAA02g05230 | A02 | 2297509 | C | T | upstream_gene_variant | MODIFIER | c.-2778G>A| |
S104 |
| 157553 | BAA02g05230 | A02 | 2297694 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S10 |
| 157554 | BAA02g05230 | A02 | 2297705 | G | A | upstream_gene_variant | MODIFIER | c.-2974C>T| |
S198 |
| 157555 | BAA02g05250 | A02 | 2297728 | G | A | synonymous_variant | LOW | c.504C>T|p.Val168Val |
S110 |
| 157556 | BAA02g05250 | A02 | 2298050 | C | T | synonymous_variant | LOW | c.264G>A|p.Glu88Glu |
S15 S3 |
| 157557 | BAA02g05250 | A02 | 2298669 | C | T | missense_variant | MODERATE | c.83G>A|p.Gly28Glu |
S293 |
| 157558 | BAA02g05230 | A02 | 2299227 | G | A | upstream_gene_variant | MODIFIER | c.-4496C>T| |
S303 |
| 157559 | BAA02g05230 | A02 | 2299605 | G | A | upstream_gene_variant | MODIFIER | c.-4874C>T| |
S132 S137 S215 |
| 157560 | BAA02g05230 | A02 | 2299729 | G | A | upstream_gene_variant | MODIFIER | c.-4998C>T| |
S59 |
| 157561 | BAA02g05240 | A02 | 2300298 | G | A | upstream_gene_variant | MODIFIER | c.-3337C>T| |
S90 |
| 157562 | BAA02g05240 | A02 | 2300369 | G | A | upstream_gene_variant | MODIFIER | c.-3408C>T| |
S273 |
| 157563 | BAA02g05240 | A02 | 2300797 | G | A | upstream_gene_variant | MODIFIER | c.-3836C>T| |
S125 |
| 157564 | BAA02g05240 | A02 | 2300913 | G | A | upstream_gene_variant | MODIFIER | c.-3952C>T| |
S244 |
| 157565 | BAA02g05260 | A02 | 2301447 | G | A | synonymous_variant | LOW | c.228G>A|p.Gln76Gln |
S184 |
| 157566 | BAA02g05260 | A02 | 2301848 | C | T | missense_variant | MODERATE | c.512C>T|p.Ser171Phe |
S272 |
| 157567 | BAA02g05260 | A02 | 2303175 | G | A | missense_variant | MODERATE | c.1193G>A|p.Gly398Asp |
S303 |
| 157568 | BAA02g05250 | A02 | 2303387 | C | T | upstream_gene_variant | MODIFIER | c.-4636G>A| |
S123 |
| 157569 | BAA02g05270 | A02 | 2304968 | G | A | missense_variant | MODERATE | c.1759C>T|p.His587Tyr |
S148 S210 S30 S31 |
| 157570 | BAA02g05270 | A02 | 2305338 | G | A | missense_variant | MODERATE | c.1478C>T|p.Pro493Leu |
S23 |
| 157571 | BAA02g05270 | A02 | 2305404 | G | A | missense_variant | MODERATE | c.1412C>T|p.Ala471Val |
S280 |
| 157572 | BAA02g05270 | A02 | 2305500 | G | A | missense_variant | MODERATE | c.1316C>T|p.Pro439Leu |
S125 |
| 157573 | BAA02g05280 | A02 | 2305668 | C | T | upstream_gene_variant | MODIFIER | c.-4254C>T| |
S178 |
| 157574 | BAA02g05270 | A02 | 2306255 | C | T | stop_gained | HIGH | c.1098G>A|p.Trp366* |
S277 S298 |
| 157575 | BAA02g05280 | A02 | 2306999 | G | A | upstream_gene_variant | MODIFIER | c.-2923G>A| |
S209 |