| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 44101 | BAA01g26840 | A01 | 15135481 | G | A | downstream_gene_variant | MODIFIER | c.*2476G>A| |
S12 |
| 44102 | BAA01g26840 | A01 | 15135490 | G | A | downstream_gene_variant | MODIFIER | c.*2485G>A| |
S262 |
| 44103 | BAA01g26840 | A01 | 15135609 | C | T | downstream_gene_variant | MODIFIER | c.*2604C>T| |
S47 |
| 44104 | BAA01g26840 | A01 | 15136256 | G | A | downstream_gene_variant | MODIFIER | c.*3251G>A| |
S175 |
| 44105 | BAA01g26840 | A01 | 15136412 | G | A | downstream_gene_variant | MODIFIER | c.*3407G>A| |
S6 |
| 44106 | BAA01g26840 | A01 | 15136747 | C | T | downstream_gene_variant | MODIFIER | c.*3742C>T| |
S273 |
| 44107 | BAA01g26850 | A01 | 15137864 | G | A | upstream_gene_variant | MODIFIER | c.-3995G>A| |
S306 |
| 44108 | BAA01g26850 | A01 | 15138202 | C | T | upstream_gene_variant | MODIFIER | c.-3657C>T| |
S158 |
| 44109 | BAA01g26850 | A01 | 15138505 | C | T | upstream_gene_variant | MODIFIER | c.-3354C>T| |
S295 |
| 44110 | BAA01g26850 | A01 | 15138640 | C | T | upstream_gene_variant | MODIFIER | c.-3219C>T| |
S38 |
| 44111 | BAA01g26850 | A01 | 15138668 | C | T | upstream_gene_variant | MODIFIER | c.-3191C>T| |
S89 |
| 44112 | BAA01g26850 | A01 | 15138937 | C | T | upstream_gene_variant | MODIFIER | c.-2922C>T| |
S234 |
| 44113 | BAA01g26850 | A01 | 15138971 | C | T | upstream_gene_variant | MODIFIER | c.-2888C>T| |
S196 |
| 44114 | BAA01g26850 | A01 | 15139272 | C | T | upstream_gene_variant | MODIFIER | c.-2587C>T| |
S256 |
| 44115 | BAA01g26850 | A01 | 15139344 | C | T | upstream_gene_variant | MODIFIER | c.-2515C>T| |
S104 S52 |
| 44116 | BAA01g26850 | A01 | 15139995 | C | T | upstream_gene_variant | MODIFIER | c.-1864C>T| |
S117 |
| 44117 | BAA01g26850 | A01 | 15140117 | C | T | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S134 |
| 44118 | BAA01g26850 | A01 | 15140182 | C | T | upstream_gene_variant | MODIFIER | c.-1677C>T| |
S53 |
| 44119 | BAA01g26850 | A01 | 15140281 | C | T | upstream_gene_variant | MODIFIER | c.-1578C>T| |
S69 |
| 44120 | BAA01g26850 | A01 | 15141031 | G | A | upstream_gene_variant | MODIFIER | c.-828G>A| |
S180 |
| 44121 | BAA01g26860 | A01 | 15144027 | C | T | downstream_gene_variant | MODIFIER | c.*3276G>A| |
S139 |
| 44122 | BAA01g26850 | A01 | 15144220 | G | A | missense_variant | MODERATE | c.1520G>A|p.Arg507Lys |
S209 |
| 44123 | BAA01g26850 | A01 | 15145101 | C | T | missense_variant | MODERATE | c.2057C>T|p.Ser686Phe |
S264 |
| 44124 | BAA01g26850 | A01 | 15145137 | C | T | missense_variant | MODERATE | c.2093C>T|p.Thr698Ile |
S69 |
| 44125 | BAA01g26850 | A01 | 15145142 | G | A | missense_variant | MODERATE | c.2098G>A|p.Val700Ile |
S60 |