| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 213401 | BAA02g31970 | A02 | 26003120 | C | T | missense_variant | MODERATE | c.2267G>A|p.Gly756Glu |
S245 |
| 213402 | BAA02g31970 | A02 | 26003371 | G | A | synonymous_variant | LOW | c.2094C>T|p.Ile698Ile |
S271 |
| 213403 | BAA02g31970 | A02 | 26005263 | G | A | intron_variant | MODIFIER | c.1419+21C>T| |
S303 |
| 213404 | BAA02g31970 | A02 | 26005396 | G | A | missense_variant | MODERATE | c.1307C>T|p.Ser436Phe |
S9 |
| 213405 | BAA02g31970 | A02 | 26005605 | C | T | missense_variant | MODERATE | c.1181G>A|p.Gly394Glu |
S25 |
| 213406 | BAA02g31970 | A02 | 26006164 | G | A | synonymous_variant | LOW | c.771C>T|p.Ser257Ser |
S162 |
| 213407 | BAA02g31970 | A02 | 26006248 | G | T | synonymous_variant | LOW | c.687C>A|p.Val229Val |
S216 |
| 213408 | BAA02g31970 | A02 | 26007309 | G | A | intron_variant | MODIFIER | c.596+379C>T| |
S189 |
| 213409 | BAA02g31970 | A02 | 26007342 | G | A | intron_variant | MODIFIER | c.596+346C>T| |
S153 S213 |
| 213410 | BAA02g31970 | A02 | 26009223 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S203 |
| 213411 | BAA02g31970 | A02 | 26009260 | C | T | upstream_gene_variant | MODIFIER | c.-152G>A| |
S238 |
| 213412 | BAA02g31970 | A02 | 26009487 | C | T | upstream_gene_variant | MODIFIER | c.-379G>A| |
S256 |
| 213413 | BAA02g31970 | A02 | 26010141 | C | T | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S186 |
| 213414 | BAA02g31970 | A02 | 26010705 | C | T | upstream_gene_variant | MODIFIER | c.-1597G>A| |
S12 |
| 213415 | BAA02g31970 | A02 | 26011790 | C | T | upstream_gene_variant | MODIFIER | c.-2682G>A| |
S61 |
| 213416 | BAA02g31970 | A02 | 26012002 | C | T | upstream_gene_variant | MODIFIER | c.-2894G>A| |
S155 S211 |
| 213417 | BAA02g31980 | A02 | 26022554 | C | T | downstream_gene_variant | MODIFIER | c.*1901G>A| |
S50 |
| 213418 | BAA02g31980 | A02 | 26023229 | C | T | downstream_gene_variant | MODIFIER | c.*1226G>A| |
S200 |
| 213419 | BAA02g31980 | A02 | 26026118 | C | T | missense_variant | MODERATE | c.228G>A|p.Met76Ile |
S150 |
| 213420 | BAA02g31980 | A02 | 26026133 | C | T | synonymous_variant | LOW | c.213G>A|p.Gln71Gln |
S184 |
| 213421 | BAA02g31980 | A02 | 26026201 | C | T | missense_variant | MODERATE | c.145G>A|p.Asp49Asn |
S256 |
| 213422 | BAA02g31980 | A02 | 26026219 | C | T | missense_variant | MODERATE | c.127G>A|p.Glu43Lys |
S184 |
| 213423 | BAA02g31980 | A02 | 26026274 | C | T | synonymous_variant | LOW | c.72G>A|p.Leu24Leu |
S165 S211 S227 S255 |
| 213424 | BAA02g31980 | A02 | 26026478 | C | T | upstream_gene_variant | MODIFIER | c.-133G>A| |
S103 S134 |
| 213425 | BAA02g31980 | A02 | 26026854 | C | T | upstream_gene_variant | MODIFIER | c.-509G>A| |
S55 |