| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 173951 | BAA02g17000 | A02 | 8442995 | G | A | downstream_gene_variant | MODIFIER | c.*861G>A| |
S190 |
| 173952 | BAA02g17000 | A02 | 8443410 | G | A | downstream_gene_variant | MODIFIER | c.*1276G>A| |
S305 |
| 173953 | BAA02g17000 | A02 | 8444106 | G | A | downstream_gene_variant | MODIFIER | c.*1972G>A| |
S188 |
| 173954 | BAA02g17000 | A02 | 8444123 | G | A | downstream_gene_variant | MODIFIER | c.*1989G>A| |
S150 |
| 173955 | BAA02g17000 | A02 | 8446170 | G | A | downstream_gene_variant | MODIFIER | c.*4036G>A| |
S23 |
| 173956 | BAA02g17000 | A02 | 8446255 | C | T | downstream_gene_variant | MODIFIER | c.*4121C>T| |
S202 |
| 173957 | BAA02g17000 | A02 | 8446515 | G | A | downstream_gene_variant | MODIFIER | c.*4381G>A| |
S296 |
| 173958 | BAA02g17000 | A02 | 8446840 | C | T | downstream_gene_variant | MODIFIER | c.*4706C>T| |
S82 |
| 173959 | BAA02g17010 | A02 | 8447431 | G | A | upstream_gene_variant | MODIFIER | c.-4570G>A| |
S33 |
| 173960 | BAA02g17010 | A02 | 8448193 | G | A | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S129 S282 |
| 173961 | BAA02g17010 | A02 | 8448516 | G | A | upstream_gene_variant | MODIFIER | c.-3485G>A| |
S287 |
| 173962 | BAA02g17010 | A02 | 8448859 | C | T | upstream_gene_variant | MODIFIER | c.-3142C>T| |
S116 |
| 173963 | BAA02g17010 | A02 | 8450126 | C | T | upstream_gene_variant | MODIFIER | c.-1875C>T| |
S216 S241 S265 S39 |
| 173964 | BAA02g17010 | A02 | 8450468 | C | T | upstream_gene_variant | MODIFIER | c.-1533C>T| |
S283 |
| 173965 | BAA02g17010 | A02 | 8452115 | G | A | splice_region_variant&intron_variant | LOW | c.108+7G>A| |
S238 |
| 173966 | BAA02g17010 | A02 | 8452725 | C | T | missense_variant | MODERATE | c.364C>T|p.Leu122Phe |
S181 |
| 173967 | BAA02g17010 | A02 | 8452848 | C | T | missense_variant | MODERATE | c.487C>T|p.Leu163Phe |
S183 S198 |
| 173968 | BAA02g17010 | A02 | 8458684 | C | T | intron_variant | MODIFIER | c.1215+427C>T| |
S25 |
| 173969 | BAA02g17010 | A02 | 8458968 | C | T | intron_variant | MODIFIER | c.1215+711C>T| |
S212 |
| 173970 | BAA02g17010 | A02 | 8459119 | C | T | intron_variant | MODIFIER | c.1215+862C>T| |
S104 |
| 173971 | BAA02g17010 | A02 | 8460321 | G | A | intron_variant | MODIFIER | c.1215+2064G>A| |
S172 S217 |
| 173972 | BAA02g17010 | A02 | 8460324 | G | A | intron_variant | MODIFIER | c.1215+2067G>A| |
S296 |
| 173973 | BAA02g17010 | A02 | 8460521 | G | A | intron_variant | MODIFIER | c.1215+2264G>A| |
S297 |
| 173974 | BAA02g17010 | A02 | 8461242 | C | T | intron_variant | MODIFIER | c.1216-1991C>T| |
S216 S265 S39 |
| 173975 | BAA02g17010 | A02 | 8461244 | C | T | intron_variant | MODIFIER | c.1216-1989C>T| |
S250 |