| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 16101 | BAA01g12250 | A01 | 5755738 | C | T | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S200 |
| 16102 | BAA01g12250 | A01 | 5756912 | G | A | missense_variant | MODERATE | c.122G>A|p.Gly41Asp |
S201 |
| 16103 | BAA01g12250 | A01 | 5756975 | C | T | missense_variant | MODERATE | c.185C>T|p.Pro62Leu |
S78 |
| 16104 | BAA01g12250 | A01 | 5757032 | C | T | missense_variant | MODERATE | c.242C>T|p.Thr81Ile |
S211 |
| 16105 | BAA01g12250 | A01 | 5757073 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S58 |
| 16106 | BAA01g12270 | A01 | 5758807 | C | T | upstream_gene_variant | MODIFIER | c.-4474C>T| |
S176 |
| 16107 | BAA01g12270 | A01 | 5758920 | G | A | upstream_gene_variant | MODIFIER | c.-4361G>A| |
S157 S163 |
| 16108 | BAA01g12270 | A01 | 5760161 | C | T | upstream_gene_variant | MODIFIER | c.-3120C>T| |
S296 |
| 16109 | BAA01g12270 | A01 | 5760408 | G | A | upstream_gene_variant | MODIFIER | c.-2873G>A| |
S103 |
| 16110 | BAA01g12260 | A01 | 5761180 | C | T | missense_variant | MODERATE | c.875G>A|p.Gly292Asp |
S177 |
| 16111 | BAA01g12260 | A01 | 5761284 | C | T | synonymous_variant | LOW | c.771G>A|p.Pro257Pro |
S250 |
| 16112 | BAA01g12270 | A01 | 5762154 | C | T | upstream_gene_variant | MODIFIER | c.-1127C>T| |
S261 |
| 16113 | BAA01g12270 | A01 | 5762351 | G | A | upstream_gene_variant | MODIFIER | c.-930G>A| |
S13 |
| 16114 | BAA01g12270 | A01 | 5763422 | G | A | splice_region_variant&intron_variant | LOW | c.136+6G>A| |
S133 |
| 16115 | BAA01g12270 | A01 | 5764085 | G | A | synonymous_variant | LOW | c.378G>A|p.Gln126Gln |
S153 |
| 16116 | BAA01g12280 | A01 | 5764521 | C | T | missense_variant | MODERATE | c.1168G>A|p.Asp390Asn |
S94 |
| 16117 | BAA01g12280 | A01 | 5764971 | G | A | missense_variant | MODERATE | c.718C>T|p.His240Tyr |
S12 |
| 16118 | BAA01g12280 | A01 | 5764984 | G | A | synonymous_variant | LOW | c.705C>T|p.Thr235Thr |
S32 |
| 16119 | BAA01g12280 | A01 | 5765195 | G | A | missense_variant | MODERATE | c.494C>T|p.Ser165Leu |
S180 |
| 16120 | BAA01g12260 | A01 | 5766027 | C | T | upstream_gene_variant | MODIFIER | c.-3055G>A| |
S51 |
| 16121 | BAA01g12260 | A01 | 5767055 | G | A | upstream_gene_variant | MODIFIER | c.-4083C>T| |
S209 |
| 16122 | BAA01g12260 | A01 | 5767090 | C | T | upstream_gene_variant | MODIFIER | c.-4118G>A| |
S294 |
| 16123 | BAA01g12290 | A01 | 5768301 | C | T | synonymous_variant | LOW | c.1146G>A|p.Glu382Glu |
S136 |
| 16124 | BAA01g12290 | A01 | 5768716 | C | T | missense_variant | MODERATE | c.731G>A|p.Gly244Glu |
S128 |
| 16125 | BAA01g12290 | A01 | 5770045 | C | T | missense_variant | MODERATE | c.82G>A|p.Gly28Ser |
S119 |