| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 53751 | BAA01g29550 | A01 | 18675537 | C | T | downstream_gene_variant | MODIFIER | c.*4619C>T| |
S266 |
| 53752 | BAA01g29550 | A01 | 18675668 | G | A | downstream_gene_variant | MODIFIER | c.*4750G>A| |
S196 |
| 53753 | BAA01g29560 | A01 | 18676035 | G | A | downstream_gene_variant | MODIFIER | c.*2002C>T| |
S1 |
| 53754 | BAA01g29560 | A01 | 18676304 | G | A | downstream_gene_variant | MODIFIER | c.*1733C>T| |
S287 |
| 53755 | BAA01g29560 | A01 | 18676726 | C | T | downstream_gene_variant | MODIFIER | c.*1311G>A| |
S200 |
| 53756 | BAA01g29560 | A01 | 18677074 | C | T | downstream_gene_variant | MODIFIER | c.*963G>A| |
S294 |
| 53757 | BAA01g29560 | A01 | 18677095 | G | A | downstream_gene_variant | MODIFIER | c.*942C>T| |
S195 |
| 53758 | BAA01g29560 | A01 | 18677282 | C | T | downstream_gene_variant | MODIFIER | c.*755G>A| |
S117 |
| 53759 | BAA01g29560 | A01 | 18677706 | C | T | downstream_gene_variant | MODIFIER | c.*331G>A| |
S148 S210 S226 |
| 53760 | BAA01g29560 | A01 | 18677834 | C | T | downstream_gene_variant | MODIFIER | c.*203G>A| |
S35 |
| 53761 | BAA01g29560 | A01 | 18677897 | C | T | downstream_gene_variant | MODIFIER | c.*140G>A| |
S273 |
| 53762 | BAA01g29560 | A01 | 18678580 | A | G | synonymous_variant | LOW | c.474T>C|p.Asp158Asp |
S284 |
| 53763 | BAA01g29560 | A01 | 18678652 | G | A | synonymous_variant | LOW | c.402C>T|p.Leu134Leu |
S149 |
| 53764 | BAA01g29560 | A01 | 18678684 | G | A | missense_variant | MODERATE | c.370C>T|p.Leu124Phe |
S97 |
| 53765 | BAA01g29580 | A01 | 18678931 | G | A | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S67 |
| 53766 | BAA01g29560 | A01 | 18679148 | G | A | upstream_gene_variant | MODIFIER | c.-27C>T| |
S216 |
| 53767 | BAA01g29570 | A01 | 18679469 | G | A | synonymous_variant | LOW | c.654C>T|p.Asn218Asn |
S281 |
| 53768 | BAA01g29570 | A01 | 18679642 | G | A | missense_variant | MODERATE | c.481C>T|p.Leu161Phe |
S208 S219 |
| 53769 | BAA01g29570 | A01 | 18679818 | C | T | splice_region_variant&intron_variant | LOW | c.385+4G>A| |
S234 |
| 53770 | BAA01g29560 | A01 | 18680087 | C | T | upstream_gene_variant | MODIFIER | c.-966G>A| |
S32 |
| 53771 | BAA01g29570 | A01 | 18680278 | C | T | synonymous_variant | LOW | c.27G>A|p.Arg9Arg |
S90 |
| 53772 | BAA01g29560 | A01 | 18681087 | G | A | upstream_gene_variant | MODIFIER | c.-1966C>T| |
S287 |
| 53773 | BAA01g29560 | A01 | 18681571 | C | T | upstream_gene_variant | MODIFIER | c.-2450G>A| |
S289 S290 |
| 53774 | BAA01g29560 | A01 | 18682182 | G | A | upstream_gene_variant | MODIFIER | c.-3061C>T| |
S278 |
| 53775 | BAA01g29580 | A01 | 18682967 | G | A | start_lost | HIGH | c.3G>A|p.Met1? |
S8 |