| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178301 | BAA02g19240 | A02 | 9993321 | C | T | upstream_gene_variant | MODIFIER | c.-408G>A| |
S183 S198 |
| 178302 | BAA02g19250 | A02 | 9993711 | C | T | missense_variant | MODERATE | c.587G>A|p.Gly196Glu |
S115 |
| 178303 | BAA02g19240 | A02 | 9995054 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S15 S3 |
| 178304 | BAA02g19240 | A02 | 9995069 | C | T | upstream_gene_variant | MODIFIER | c.-2156G>A| |
S181 |
| 178305 | BAA02g19240 | A02 | 9996242 | T | A | upstream_gene_variant | MODIFIER | c.-3329A>T| |
S38 |
| 178306 | BAA02g19240 | A02 | 9997417 | C | T | upstream_gene_variant | MODIFIER | c.-4504G>A| |
S76 |
| 178307 | BAA02g19240 | A02 | 9997430 | C | T | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S270 |
| 178308 | BAA02g19250 | A02 | 9998956 | C | T | upstream_gene_variant | MODIFIER | c.-3723G>A| |
S71 |
| 178309 | BAA02g19250 | A02 | 9999120 | G | A | upstream_gene_variant | MODIFIER | c.-3887C>T| |
S303 |
| 178310 | BAA02g19250 | A02 | 9999205 | C | T | upstream_gene_variant | MODIFIER | c.-3972G>A| |
S283 |
| 178311 | BAA02g19250 | A02 | 9999270 | C | T | upstream_gene_variant | MODIFIER | c.-4037G>A| |
S289 S290 |
| 178312 | BAA02g19250 | A02 | 9999495 | G | A | upstream_gene_variant | MODIFIER | c.-4262C>T| |
S295 |
| 178313 | BAA02g19250 | A02 | 9999606 | G | A | upstream_gene_variant | MODIFIER | c.-4373C>T| |
S231 |
| 178314 | BAA02g19250 | A02 | 9999845 | G | A | upstream_gene_variant | MODIFIER | c.-4612C>T| |
S23 |
| 178315 | BAA02g19280 | A02 | 10001422 | C | T | upstream_gene_variant | MODIFIER | c.-2289C>T| |
S183 S198 |
| 178316 | BAA02g19280 | A02 | 10001736 | C | T | upstream_gene_variant | MODIFIER | c.-1975C>T| |
S94 |
| 178317 | BAA02g19280 | A02 | 10002158 | C | T | upstream_gene_variant | MODIFIER | c.-1553C>T| |
S162 |
| 178318 | BAA02g19270 | A02 | 10004175 | G | A | upstream_gene_variant | MODIFIER | c.-992C>T| |
S298 |
| 178319 | BAA02g19270 | A02 | 10004331 | C | T | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S34 |
| 178320 | BAA02g19290 | A02 | 10005761 | C | T | synonymous_variant | LOW | c.435C>T|p.Phe145Phe |
S249 |
| 178321 | BAA02g19290 | A02 | 10005797 | C | T | synonymous_variant | LOW | c.471C>T|p.Asn157Asn |
S174 S27 |
| 178322 | BAA02g19270 | A02 | 10007160 | C | T | upstream_gene_variant | MODIFIER | c.-3977G>A| |
S79 S84 |
| 178323 | BAA02g19310 | A02 | 10008187 | C | T | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S77 S82 |
| 178324 | BAA02g19310 | A02 | 10011024 | C | T | upstream_gene_variant | MODIFIER | c.-1755C>T| |
S290 |
| 178325 | BAA02g19310 | A02 | 10011361 | G | A | upstream_gene_variant | MODIFIER | c.-1418G>A| |
S48 |