| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 76201 | BAA01g40090 | A01 | 26687091 | C | T | downstream_gene_variant | MODIFIER | c.*3668C>T| |
S242 |
| 76202 | BAA01g40110 | A01 | 26688987 | G | A | synonymous_variant | LOW | c.828C>T|p.Ser276Ser |
S9 |
| 76203 | BAA01g40110 | A01 | 26689213 | C | T | missense_variant | MODERATE | c.602G>A|p.Gly201Glu |
S134 S162 |
| 76204 | BAA01g40110 | A01 | 26689305 | C | T | synonymous_variant | LOW | c.510G>A|p.Lys170Lys |
S156 |
| 76205 | BAA01g40110 | A01 | 26691672 | C | T | upstream_gene_variant | MODIFIER | c.-1282G>A| |
S112 |
| 76206 | BAA01g40110 | A01 | 26692753 | C | T | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S200 S303 |
| 76207 | BAA01g40120 | A01 | 26692845 | G | A | synonymous_variant | LOW | c.273G>A|p.Lys91Lys |
S76 |
| 76208 | BAA01g40120 | A01 | 26692990 | G | A | missense_variant | MODERATE | c.418G>A|p.Gly140Arg |
S60 |
| 76209 | BAA01g40120 | A01 | 26693202 | C | T | synonymous_variant | LOW | c.630C>T|p.Thr210Thr |
S274 |
| 76210 | BAA01g40120 | A01 | 26693585 | C | T | missense_variant | MODERATE | c.1013C>T|p.Pro338Leu |
S231 |
| 76211 | BAA01g40110 | A01 | 26694441 | C | T | upstream_gene_variant | MODIFIER | c.-4051G>A| |
S192 |
| 76212 | BAA01g40130 | A01 | 26695448 | C | T | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S261 |
| 76213 | BAA01g40130 | A01 | 26696135 | C | T | synonymous_variant | LOW | c.781C>T|p.Leu261Leu |
S221 |
| 76214 | BAA01g40120 | A01 | 26697004 | C | T | downstream_gene_variant | MODIFIER | c.*2604C>T| |
S118 |
| 76215 | BAA01g40120 | A01 | 26697204 | C | T | downstream_gene_variant | MODIFIER | c.*2804C>T| |
S16 |
| 76216 | BAA01g40140 | A01 | 26699893 | G | A | splice_region_variant&intron_variant | LOW | c.933+5C>T| |
S267 |
| 76217 | BAA01g40150 | A01 | 26700081 | C | T | upstream_gene_variant | MODIFIER | c.-4656C>T| |
S153 |
| 76218 | BAA01g40140 | A01 | 26700148 | G | A | synonymous_variant | LOW | c.759C>T|p.Phe253Phe |
S139 |
| 76219 | BAA01g40140 | A01 | 26700273 | C | T | missense_variant | MODERATE | c.634G>A|p.Gly212Arg |
S8 |
| 76220 | BAA01g40140 | A01 | 26701049 | G | A | missense_variant | MODERATE | c.151C>T|p.Pro51Ser |
S86 |
| 76221 | BAA01g40140 | A01 | 26701225 | C | T | missense_variant | MODERATE | c.40G>A|p.Val14Ile |
S161 |
| 76222 | BAA01g40140 | A01 | 26701364 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S257 |
| 76223 | BAA01g40140 | A01 | 26701520 | G | A | upstream_gene_variant | MODIFIER | c.-256C>T| |
S169 |
| 76224 | BAA01g40140 | A01 | 26701545 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S263 |
| 76225 | BAA01g40140 | A01 | 26702339 | C | T | upstream_gene_variant | MODIFIER | c.-1075G>A| |
S144 |