| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177951 | BAA02g19060 | A02 | 9881622 | G | A | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S41 |
| 177952 | BAA02g19060 | A02 | 9881754 | G | A | upstream_gene_variant | MODIFIER | c.-4059C>T| |
S295 |
| 177953 | BAA02g19070 | A02 | 9882773 | G | A | upstream_gene_variant | MODIFIER | c.-1355G>A| |
S206 S26 |
| 177954 | BAA02g19070 | A02 | 9882795 | G | A | upstream_gene_variant | MODIFIER | c.-1333G>A| |
S259 |
| 177955 | BAA02g19070 | A02 | 9883272 | G | A | upstream_gene_variant | MODIFIER | c.-856G>A| |
S133 |
| 177956 | BAA02g19070 | A02 | 9885237 | G | A | downstream_gene_variant | MODIFIER | c.*796G>A| |
S271 |
| 177957 | BAA02g19070 | A02 | 9886215 | G | A | downstream_gene_variant | MODIFIER | c.*1774G>A| |
S265 |
| 177958 | BAA02g19080 | A02 | 9887107 | C | T | synonymous_variant | LOW | c.453G>A|p.Leu151Leu |
S166 |
| 177959 | BAA02g19080 | A02 | 9887504 | G | A | missense_variant | MODERATE | c.56C>T|p.Ser19Phe |
S162 |
| 177960 | BAA02g19080 | A02 | 9889499 | C | T | upstream_gene_variant | MODIFIER | c.-1940G>A| |
S186 |
| 177961 | BAA02g19080 | A02 | 9889599 | G | A | upstream_gene_variant | MODIFIER | c.-2040C>T| |
S215 S36 |
| 177962 | BAA02g19080 | A02 | 9890300 | G | A | upstream_gene_variant | MODIFIER | c.-2741C>T| |
S134 |
| 177963 | BAA02g19080 | A02 | 9890553 | C | T | upstream_gene_variant | MODIFIER | c.-2994G>A| |
S155 S211 |
| 177964 | BAA02g19080 | A02 | 9890811 | G | A | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S11 |
| 177965 | BAA02g19080 | A02 | 9892415 | C | T | upstream_gene_variant | MODIFIER | c.-4856G>A| |
S104 S52 |
| 177966 | BAA02g19090 | A02 | 9892787 | C | T | upstream_gene_variant | MODIFIER | c.-2453C>T| |
S284 |
| 177967 | BAA02g19090 | A02 | 9892854 | C | T | upstream_gene_variant | MODIFIER | c.-2386C>T| |
S302 |
| 177968 | BAA02g19090 | A02 | 9892937 | G | A | upstream_gene_variant | MODIFIER | c.-2303G>A| |
S74 |
| 177969 | BAA02g19090 | A02 | 9893863 | G | A | upstream_gene_variant | MODIFIER | c.-1377G>A| |
S62 |
| 177970 | BAA02g19090 | A02 | 9894028 | G | A | upstream_gene_variant | MODIFIER | c.-1212G>A| |
S279 |
| 177971 | BAA02g19090 | A02 | 9894249 | G | A | upstream_gene_variant | MODIFIER | c.-991G>A| |
S204 |
| 177972 | BAA02g19090 | A02 | 9894279 | C | T | upstream_gene_variant | MODIFIER | c.-961C>T| |
S211 S227 |
| 177973 | BAA02g19090 | A02 | 9894298 | G | A | upstream_gene_variant | MODIFIER | c.-942G>A| |
S126 |
| 177974 | BAA02g19090 | A02 | 9894352 | G | A | upstream_gene_variant | MODIFIER | c.-888G>A| |
S143 |
| 177975 | BAA02g19090 | A02 | 9894381 | G | A | upstream_gene_variant | MODIFIER | c.-859G>A| |
S170 |