| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154601 | BAA02g02840 | A02 | 1283944 | C | T | upstream_gene_variant | MODIFIER | c.-835G>A| |
S33 |
| 154602 | BAA02g02840 | A02 | 1285495 | G | A | upstream_gene_variant | MODIFIER | c.-2386C>T| |
S173 |
| 154603 | BAA02g02840 | A02 | 1285603 | C | T | upstream_gene_variant | MODIFIER | c.-2494G>A| |
S131 |
| 154604 | BAA02g02840 | A02 | 1286083 | C | T | upstream_gene_variant | MODIFIER | c.-2974G>A| |
S199 |
| 154605 | BAA02g02850 | A02 | 1287532 | G | A | synonymous_variant | LOW | c.189G>A|p.Glu63Glu |
S264 |
| 154606 | BAA02g02860 | A02 | 1288639 | C | T | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S108 |
| 154607 | BAA02g02860 | A02 | 1288890 | C | T | upstream_gene_variant | MODIFIER | c.-841C>T| |
S77 S82 |
| 154608 | BAA02g02860 | A02 | 1289102 | G | A | upstream_gene_variant | MODIFIER | c.-629G>A| |
S162 |
| 154609 | BAA02g02860 | A02 | 1290049 | A | C | missense_variant | MODERATE | c.319A>C|p.Lys107Gln |
S143 S250 S262 |
| 154610 | BAA02g02860 | A02 | 1290165 | G | A | synonymous_variant | LOW | c.435G>A|p.Ala145Ala |
S136 |
| 154611 | BAA02g02860 | A02 | 1290258 | C | T | synonymous_variant | LOW | c.528C>T|p.Val176Val |
S250 |
| 154612 | BAA02g02850 | A02 | 1290919 | G | A | downstream_gene_variant | MODIFIER | c.*2547G>A| |
S163 |
| 154613 | BAA02g02850 | A02 | 1291155 | C | T | downstream_gene_variant | MODIFIER | c.*2783C>T| |
S76 |
| 154614 | BAA02g02850 | A02 | 1291422 | G | A | downstream_gene_variant | MODIFIER | c.*3050G>A| |
S210 S225 |
| 154615 | BAA02g02850 | A02 | 1291430 | C | T | downstream_gene_variant | MODIFIER | c.*3058C>T| |
S245 |
| 154616 | BAA02g02850 | A02 | 1292169 | G | A | downstream_gene_variant | MODIFIER | c.*3797G>A| |
S89 |
| 154617 | BAA02g02870 | A02 | 1293090 | A | T | missense_variant | MODERATE | c.331T>A|p.Tyr111Asn |
S206 |
| 154618 | BAA02g02850 | A02 | 1293176 | G | A | downstream_gene_variant | MODIFIER | c.*4804G>A| |
S62 |
| 154619 | BAA02g02870 | A02 | 1296805 | G | A | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S296 |
| 154620 | BAA02g02880 | A02 | 1297135 | C | T | missense_variant | MODERATE | c.69G>A|p.Met23Ile |
S116 |
| 154621 | BAA02g02880 | A02 | 1297150 | C | T | missense_variant | MODERATE | c.54G>A|p.Met18Ile |
S243 S299 |
| 154622 | BAA02g02870 | A02 | 1297759 | G | A | upstream_gene_variant | MODIFIER | c.-3985C>T| |
S23 |
| 154623 | BAA02g02870 | A02 | 1298412 | C | T | upstream_gene_variant | MODIFIER | c.-4638G>A| |
S13 |
| 154624 | BAA02g02880 | A02 | 1298937 | G | A | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S148 S30 S31 |
| 154625 | BAA02g02880 | A02 | 1300017 | G | A | upstream_gene_variant | MODIFIER | c.-2814C>T| |
S8 |