| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 166051 | BAA02g12190 | A02 | 5494029 | G | A | missense_variant | MODERATE | c.295C>T|p.Pro99Ser |
S305 |
| 166052 | BAA02g12190 | A02 | 5494231 | G | A | synonymous_variant | LOW | c.93C>T|p.Pro31Pro |
S209 |
| 166053 | BAA02g12200 | A02 | 5495801 | G | A | missense_variant | MODERATE | c.1894C>T|p.Pro632Ser |
S235 |
| 166054 | BAA02g12200 | A02 | 5497053 | C | T | missense_variant | MODERATE | c.1000G>A|p.Val334Ile |
S262 |
| 166055 | BAA02g12200 | A02 | 5497388 | C | T | missense_variant | MODERATE | c.665G>A|p.Gly222Asp |
S257 |
| 166056 | BAA02g12200 | A02 | 5497606 | G | A | missense_variant | MODERATE | c.533C>T|p.Thr178Ile |
S173 |
| 166057 | BAA02g12200 | A02 | 5498943 | C | T | splice_region_variant&intron_variant | LOW | c.102+8G>A| |
S1 S90 |
| 166058 | BAA02g12200 | A02 | 5499005 | G | A | synonymous_variant | LOW | c.48C>T|p.Leu16Leu |
S80 |
| 166059 | BAA02g12190 | A02 | 5499137 | C | T | upstream_gene_variant | MODIFIER | c.-4814G>A| |
S77 S82 |
| 166060 | BAA02g12190 | A02 | 5499151 | G | A | upstream_gene_variant | MODIFIER | c.-4828C>T| |
S203 |
| 166061 | BAA02g12210 | A02 | 5499822 | C | T | missense_variant | MODERATE | c.1817G>A|p.Arg606Lys |
S34 |
| 166062 | BAA02g12210 | A02 | 5500798 | C | T | missense_variant | MODERATE | c.1105G>A|p.Gly369Arg |
S209 |
| 166063 | BAA02g12210 | A02 | 5501210 | C | T | missense_variant | MODERATE | c.772G>A|p.Ala258Thr |
S301 S304 |
| 166064 | BAA02g12210 | A02 | 5501340 | C | T | synonymous_variant | LOW | c.642G>A|p.Pro214Pro |
S12 |
| 166065 | BAA02g12210 | A02 | 5501713 | G | A | missense_variant | MODERATE | c.347C>T|p.Ala116Val |
S105 S106 |
| 166066 | BAA02g12200 | A02 | 5502363 | C | T | upstream_gene_variant | MODIFIER | c.-3311G>A| |
S6 |
| 166067 | BAA02g12220 | A02 | 5504711 | C | T | missense_variant | MODERATE | c.1768G>A|p.Gly590Ser |
S266 |
| 166068 | BAA02g12220 | A02 | 5504737 | G | A | missense_variant | MODERATE | c.1742C>T|p.Thr581Ile |
S294 |
| 166069 | BAA02g12220 | A02 | 5505109 | G | A | missense_variant | MODERATE | c.1472C>T|p.Ser491Phe |
S132 S137 S215 |
| 166070 | BAA02g12220 | A02 | 5507408 | C | T | upstream_gene_variant | MODIFIER | c.-213G>A| |
S130 |
| 166071 | BAA02g12220 | A02 | 5507458 | G | A | upstream_gene_variant | MODIFIER | c.-263C>T| |
S246 |
| 166072 | BAA02g12220 | A02 | 5507508 | C | T | upstream_gene_variant | MODIFIER | c.-313G>A| |
S270 |
| 166073 | BAA02g12220 | A02 | 5509862 | T | C | upstream_gene_variant | MODIFIER | c.-2667A>G| |
S246 |
| 166074 | BAA02g12220 | A02 | 5510431 | G | A | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S287 |
| 166075 | BAA02g12220 | A02 | 5510934 | G | A | upstream_gene_variant | MODIFIER | c.-3739C>T| |
S190 |