| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 38601 | BAA01g24890 | A01 | 13301196 | C | T | missense_variant | MODERATE | c.1060G>A|p.Glu354Lys |
S75 |
| 38602 | BAA01g24890 | A01 | 13301399 | G | A | missense_variant | MODERATE | c.857C>T|p.Ser286Phe |
S56 |
| 38603 | BAA01g24890 | A01 | 13301470 | G | A | synonymous_variant | LOW | c.786C>T|p.Asp262Asp |
S157 |
| 38604 | BAA01g24890 | A01 | 13301825 | C | T | missense_variant | MODERATE | c.431G>A|p.Arg144Lys |
S16 |
| 38605 | BAA01g24890 | A01 | 13302011 | G | A | missense_variant | MODERATE | c.245C>T|p.Pro82Leu |
S208 S219 |
| 38606 | BAA01g24880 | A01 | 13303540 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S32 |
| 38607 | BAA01g24880 | A01 | 13303922 | C | T | upstream_gene_variant | MODIFIER | c.-4965G>A| |
S150 |
| 38608 | BAA01g24880 | A01 | 13303924 | G | A | upstream_gene_variant | MODIFIER | c.-4967C>T| |
S181 |
| 38609 | BAA01g24890 | A01 | 13304513 | G | A | upstream_gene_variant | MODIFIER | c.-2258C>T| |
S100 |
| 38610 | BAA01g24890 | A01 | 13304595 | C | T | upstream_gene_variant | MODIFIER | c.-2340G>A| |
S44 |
| 38611 | BAA01g24890 | A01 | 13304654 | G | A | upstream_gene_variant | MODIFIER | c.-2399C>T| |
S208 |
| 38612 | BAA01g24890 | A01 | 13304717 | C | T | upstream_gene_variant | MODIFIER | c.-2462G>A| |
S284 |
| 38613 | BAA01g24890 | A01 | 13304838 | C | T | upstream_gene_variant | MODIFIER | c.-2583G>A| |
S166 |
| 38614 | BAA01g24890 | A01 | 13305058 | C | T | upstream_gene_variant | MODIFIER | c.-2803G>A| |
S134 |
| 38615 | BAA01g24890 | A01 | 13305954 | G | A | upstream_gene_variant | MODIFIER | c.-3699C>T| |
S228 |
| 38616 | BAA01g24890 | A01 | 13307217 | G | A | upstream_gene_variant | MODIFIER | c.-4962C>T| |
S74 |
| 38617 | BAA01g24890-BAA01g24900 | A01 | 13307665 | G | A | intergenic_region | MODIFIER | n.13307665G>A| |
S13 |
| 38618 | BAA01g24890-BAA01g24900 | A01 | 13307826 | G | A | intergenic_region | MODIFIER | n.13307826G>A| |
S34 |
| 38619 | BAA01g24900 | A01 | 13311652 | G | A | upstream_gene_variant | MODIFIER | c.-3181G>A| |
S234 |
| 38620 | BAA01g24900 | A01 | 13312226 | G | A | upstream_gene_variant | MODIFIER | c.-2607G>A| |
S159 S243 S276 S298 S299 |
| 38621 | BAA01g24900 | A01 | 13312279 | C | T | upstream_gene_variant | MODIFIER | c.-2554C>T| |
S85 |
| 38622 | BAA01g24900 | A01 | 13312623 | T | A | upstream_gene_variant | MODIFIER | c.-2210T>A| |
S186 |
| 38623 | BAA01g24900 | A01 | 13312879 | G | A | upstream_gene_variant | MODIFIER | c.-1954G>A| |
S186 |
| 38624 | BAA01g24900 | A01 | 13312901 | C | T | upstream_gene_variant | MODIFIER | c.-1932C>T| |
S305 |
| 38625 | BAA01g24900 | A01 | 13313356 | C | T | upstream_gene_variant | MODIFIER | c.-1477C>T| |
S143 |