| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 20301 | BAA01g15020 | A01 | 7159678 | C | T | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S299 |
| 20302 | BAA01g15010 | A01 | 7159739 | G | A | downstream_gene_variant | MODIFIER | c.*3615G>A| |
S202 |
| 20303 | BAA01g15020 | A01 | 7160163 | C | T | splice_region_variant&synonymous_variant | LOW | c.648G>A|p.Gly216Gly |
S231 |
| 20304 | BAA01g15010 | A01 | 7160434 | G | A | downstream_gene_variant | MODIFIER | c.*4310G>A| |
S171 |
| 20305 | BAA01g15020 | A01 | 7160774 | C | T | missense_variant | MODERATE | c.341G>A|p.Arg114His |
S249 |
| 20306 | BAA01g15020 | A01 | 7161677 | C | T | upstream_gene_variant | MODIFIER | c.-496G>A| |
S54 |
| 20307 | BAA01g15020 | A01 | 7162135 | C | T | upstream_gene_variant | MODIFIER | c.-954G>A| |
S62 |
| 20308 | BAA01g15020 | A01 | 7163984 | G | A | upstream_gene_variant | MODIFIER | c.-2803C>T| |
S5 |
| 20309 | BAA01g15020 | A01 | 7164319 | C | T | upstream_gene_variant | MODIFIER | c.-3138G>A| |
S33 |
| 20310 | BAA01g15030 | A01 | 7166879 | C | T | downstream_gene_variant | MODIFIER | c.*2009G>A| |
S160 |
| 20311 | BAA01g15030 | A01 | 7167414 | C | T | downstream_gene_variant | MODIFIER | c.*1474G>A| |
S7 |
| 20312 | BAA01g15030 | A01 | 7168468 | C | T | downstream_gene_variant | MODIFIER | c.*420G>A| |
S158 |
| 20313 | BAA01g15030 | A01 | 7170215 | C | T | missense_variant | MODERATE | c.1030G>A|p.Glu344Lys |
S10 |
| 20314 | BAA01g15030 | A01 | 7172011 | G | A | upstream_gene_variant | MODIFIER | c.-668C>T| |
S32 |
| 20315 | BAA01g15030 | A01 | 7172631 | G | A | upstream_gene_variant | MODIFIER | c.-1288C>T| |
S209 |
| 20316 | BAA01g15030 | A01 | 7172709 | G | A | upstream_gene_variant | MODIFIER | c.-1366C>T| |
S75 S81 |
| 20317 | BAA01g15030 | A01 | 7173774 | G | A | upstream_gene_variant | MODIFIER | c.-2431C>T| |
S217 |
| 20318 | BAA01g15040 | A01 | 7174729 | C | T | missense_variant | MODERATE | c.899G>A|p.Gly300Asp |
S40 S49 |
| 20319 | BAA01g15040 | A01 | 7175176 | G | A | stop_gained | HIGH | c.616C>T|p.Gln206* |
S262 |
| 20320 | BAA01g15040 | A01 | 7175513 | G | A | synonymous_variant | LOW | c.279C>T|p.Leu93Leu |
S45 |
| 20321 | BAA01g15030 | A01 | 7176236 | C | T | upstream_gene_variant | MODIFIER | c.-4893G>A| |
S210 S225 S55 |
| 20322 | BAA01g15040 | A01 | 7176844 | C | T | upstream_gene_variant | MODIFIER | c.-1053G>A| |
S18 |
| 20323 | BAA01g15040 | A01 | 7176996 | G | A | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S207 |
| 20324 | BAA01g15050 | A01 | 7177456 | C | T | synonymous_variant | LOW | c.93C>T|p.Tyr31Tyr |
S167 |
| 20325 | BAA01g15050 | A01 | 7177485 | C | T | missense_variant | MODERATE | c.122C>T|p.Thr41Ile |
S187 S188 S276 |