| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154451 | BAA02g02710 | A02 | 1230350 | C | T | upstream_gene_variant | MODIFIER | c.-3570C>T| |
S212 |
| 154452 | BAA02g02710 | A02 | 1230502 | G | A | upstream_gene_variant | MODIFIER | c.-3418G>A| |
S187 |
| 154453 | BAA02g02710 | A02 | 1232834 | C | T | upstream_gene_variant | MODIFIER | c.-1086C>T| |
S152 |
| 154454 | BAA02g02710 | A02 | 1233804 | C | T | upstream_gene_variant | MODIFIER | c.-116C>T| |
S167 |
| 154455 | BAA02g02710 | A02 | 1234470 | C | T | missense_variant | MODERATE | c.460C>T|p.Pro154Ser |
S250 |
| 154456 | BAA02g02710 | A02 | 1234623 | C | T | missense_variant | MODERATE | c.613C>T|p.Leu205Phe |
S160 |
| 154457 | BAA02g02710 | A02 | 1234871 | G | A | synonymous_variant | LOW | c.861G>A|p.Gln287Gln |
S296 |
| 154458 | BAA02g02710 | A02 | 1235222 | G | A | synonymous_variant | LOW | c.1212G>A|p.Gln404Gln |
S162 |
| 154459 | BAA02g02710 | A02 | 1235381 | G | A | synonymous_variant | LOW | c.1371G>A|p.Gly457Gly |
S151 S241 |
| 154460 | BAA02g02710 | A02 | 1238231 | G | A | missense_variant | MODERATE | c.3820G>A|p.Asp1274Asn |
S162 |
| 154461 | BAA02g02710 | A02 | 1238417 | C | T | synonymous_variant | LOW | c.3921C>T|p.Asp1307Asp |
S116 |
| 154462 | BAA02g02710 | A02 | 1238690 | C | T | missense_variant | MODERATE | c.4091C>T|p.Ser1364Leu |
S249 |
| 154463 | BAA02g02730 | A02 | 1239064 | C | T | upstream_gene_variant | MODIFIER | c.-1990C>T| |
S224 |
| 154464 | BAA02g02720 | A02 | 1239951 | G | A | synonymous_variant | LOW | c.543C>T|p.Val181Val |
S247 |
| 154465 | BAA02g02720 | A02 | 1240085 | C | T | missense_variant | MODERATE | c.409G>A|p.Val137Met |
S274 |
| 154466 | BAA02g02730 | A02 | 1242028 | C | T | missense_variant | MODERATE | c.314C>T|p.Ala105Val |
S245 |
| 154467 | BAA02g02720 | A02 | 1243876 | C | T | upstream_gene_variant | MODIFIER | c.-3145G>A| |
S199 |
| 154468 | BAA02g02720 | A02 | 1244136 | C | T | upstream_gene_variant | MODIFIER | c.-3405G>A| |
S262 |
| 154469 | BAA02g02720 | A02 | 1244234 | C | T | upstream_gene_variant | MODIFIER | c.-3503G>A| |
S2 |
| 154470 | BAA02g02720 | A02 | 1244360 | C | T | upstream_gene_variant | MODIFIER | c.-3629G>A| |
S103 |
| 154471 | BAA02g02750 | A02 | 1245595 | G | A | missense_variant | MODERATE | c.367G>A|p.Gly123Ser |
S125 |
| 154472 | BAA02g02740 | A02 | 1246532 | C | T | upstream_gene_variant | MODIFIER | c.-3027G>A| |
S185 |
| 154473 | BAA02g02740 | A02 | 1246694 | C | T | upstream_gene_variant | MODIFIER | c.-3189G>A| |
S38 |
| 154474 | BAA02g02740 | A02 | 1246758 | C | T | upstream_gene_variant | MODIFIER | c.-3253G>A| |
S14 |
| 154475 | BAA02g02740 | A02 | 1247605 | G | A | upstream_gene_variant | MODIFIER | c.-4100C>T| |
S136 |