| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 188001 | BAA02g24750 | A02 | 13525870 | C | T | upstream_gene_variant | MODIFIER | c.-259C>T| |
S180 |
| 188002 | BAA02g24750 | A02 | 13526036 | C | T | upstream_gene_variant | MODIFIER | c.-93C>T| |
S138 |
| 188003 | BAA02g24760 | A02 | 13527957 | G | A | missense_variant | MODERATE | c.503C>T|p.Ser168Phe |
S187 |
| 188004 | BAA02g24760 | A02 | 13528159 | C | T | synonymous_variant | LOW | c.378G>A|p.Glu126Glu |
S15 S3 |
| 188005 | BAA02g24760 | A02 | 13529071 | G | A | upstream_gene_variant | MODIFIER | c.-430C>T| |
S79 S91 |
| 188006 | BAA02g24760 | A02 | 13530381 | G | A | upstream_gene_variant | MODIFIER | c.-1740C>T| |
S251 |
| 188007 | BAA02g24760 | A02 | 13531545 | C | T | upstream_gene_variant | MODIFIER | c.-2904G>A| |
S66 |
| 188008 | BAA02g24770 | A02 | 13532809 | C | T | missense_variant | MODERATE | c.251G>A|p.Ser84Asn |
S185 |
| 188009 | BAA02g24760 | A02 | 13533222 | C | T | upstream_gene_variant | MODIFIER | c.-4581G>A| |
S105 S106 |
| 188010 | BAA02g24760 | A02 | 13533285 | G | A | upstream_gene_variant | MODIFIER | c.-4644C>T| |
S149 |
| 188011 | BAA02g24770 | A02 | 13534837 | G | A | upstream_gene_variant | MODIFIER | c.-1778C>T| |
S298 |
| 188012 | BAA02g24770 | A02 | 13535184 | G | A | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S44 |
| 188013 | BAA02g24770 | A02 | 13535258 | G | A | upstream_gene_variant | MODIFIER | c.-2199C>T| |
S247 |
| 188014 | BAA02g24770 | A02 | 13535879 | G | A | upstream_gene_variant | MODIFIER | c.-2820C>T| |
S260 |
| 188015 | BAA02g24780 | A02 | 13538173 | C | T | upstream_gene_variant | MODIFIER | c.-2449C>T| |
S172 S217 |
| 188016 | BAA02g24780 | A02 | 13538822 | G | A | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S294 |
| 188017 | BAA02g24790 | A02 | 13541468 | C | T | upstream_gene_variant | MODIFIER | c.-1122C>T| |
S250 S252 |
| 188018 | BAA02g24790 | A02 | 13541498 | C | T | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S273 |
| 188019 | BAA02g24790 | A02 | 13543119 | C | T | missense_variant | MODERATE | c.530C>T|p.Thr177Ile |
S183 S198 |
| 188020 | BAA02g24780 | A02 | 13544762 | C | T | downstream_gene_variant | MODIFIER | c.*3772C>T| |
S185 |
| 188021 | BAA02g24790 | A02 | 13547626 | C | T | downstream_gene_variant | MODIFIER | c.*2975C>T| |
S87 |
| 188022 | BAA02g24790 | A02 | 13547941 | G | A | downstream_gene_variant | MODIFIER | c.*3290G>A| |
S191 |
| 188023 | BAA02g24790-BAA02g24800 | A02 | 13550665 | G | A | intergenic_region | MODIFIER | n.13550665G>A| |
S155 S211 |
| 188024 | BAA02g24790-BAA02g24800 | A02 | 13552137 | G | A | intergenic_region | MODIFIER | n.13552137G>A| |
S103 |
| 188025 | BAA02g24790-BAA02g24800 | A02 | 13552254 | G | A | intergenic_region | MODIFIER | n.13552254G>A| |
S134 |