| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10251 | BAA01g08340 | A01 | 3663000 | G | A | upstream_gene_variant | MODIFIER | c.-2406C>T| |
S202 |
| 10252 | BAA01g08350 | A01 | 3663776 | C | T | synonymous_variant | LOW | c.336C>T|p.Phe112Phe |
S164 |
| 10253 | BAA01g08340 | A01 | 3663927 | C | T | upstream_gene_variant | MODIFIER | c.-3333G>A| |
S158 |
| 10254 | BAA01g08350 | A01 | 3664335 | G | A | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S259 |
| 10255 | BAA01g08350 | A01 | 3664605 | C | T | missense_variant | MODERATE | c.872C>T|p.Thr291Ile |
S53 |
| 10256 | BAA01g08350 | A01 | 3664951 | C | T | synonymous_variant | LOW | c.1132C>T|p.Leu378Leu |
S265 |
| 10257 | BAA01g08350 | A01 | 3665000 | C | T | missense_variant | MODERATE | c.1181C>T|p.Ala394Val |
S8 |
| 10258 | BAA01g08350 | A01 | 3665982 | G | A | missense_variant | MODERATE | c.1769G>A|p.Gly590Glu |
S32 |
| 10259 | BAA01g08350 | A01 | 3665998 | G | A | synonymous_variant | LOW | c.1785G>A|p.Val595Val |
S251 |
| 10260 | BAA01g08350 | A01 | 3666158 | C | T | missense_variant | MODERATE | c.1945C>T|p.His649Tyr |
S25 |
| 10261 | BAA01g08350 | A01 | 3666353 | C | T | missense_variant | MODERATE | c.2140C>T|p.Pro714Ser |
S72 |
| 10262 | BAA01g08350 | A01 | 3666668 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S99 |
| 10263 | BAA01g08350 | A01 | 3666868 | C | T | downstream_gene_variant | MODIFIER | c.*378C>T| |
S266 |
| 10264 | BAA01g08350 | A01 | 3668162 | C | T | downstream_gene_variant | MODIFIER | c.*1672C>T| |
S68 |
| 10265 | BAA01g08350 | A01 | 3668394 | C | T | downstream_gene_variant | MODIFIER | c.*1904C>T| |
S128 |
| 10266 | BAA01g08350 | A01 | 3668683 | G | A | downstream_gene_variant | MODIFIER | c.*2193G>A| |
S73 |
| 10267 | BAA01g08350 | A01 | 3668715 | C | T | downstream_gene_variant | MODIFIER | c.*2225C>T| |
S189 |
| 10268 | BAA01g08360 | A01 | 3669686 | C | T | upstream_gene_variant | MODIFIER | c.-4395C>T| |
S210 |
| 10269 | BAA01g08360 | A01 | 3669905 | C | T | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S171 |
| 10270 | BAA01g08360 | A01 | 3671606 | G | A | upstream_gene_variant | MODIFIER | c.-2475G>A| |
S262 |
| 10271 | BAA01g08370 | A01 | 3674515 | C | T | upstream_gene_variant | MODIFIER | c.-4884C>T| |
S51 |
| 10272 | BAA01g08370 | A01 | 3674524 | C | T | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S133 |
| 10273 | BAA01g08360 | A01 | 3674836 | G | A | splice_region_variant&intron_variant | LOW | c.451+6G>A| |
S301 |
| 10274 | BAA01g08360 | A01 | 3676796 | C | T | synonymous_variant | LOW | c.1290C>T|p.Ser430Ser |
S128 |
| 10275 | BAA01g08360 | A01 | 3677140 | G | A | missense_variant | MODERATE | c.1549G>A|p.Val517Ile |
S247 |