| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 23051 | BAA01g16650 | A01 | 8107724 | G | A | upstream_gene_variant | MODIFIER | c.-2471C>T| |
S131 |
| 23052 | BAA01g16650 | A01 | 8109106 | C | T | upstream_gene_variant | MODIFIER | c.-3853G>A| |
S46 |
| 23053 | BAA01g16650 | A01 | 8109432 | C | T | upstream_gene_variant | MODIFIER | c.-4179G>A| |
S61 |
| 23054 | BAA01g16660 | A01 | 8109857 | C | T | missense_variant | MODERATE | c.677G>A|p.Arg226Lys |
S47 |
| 23055 | BAA01g16660 | A01 | 8110297 | C | T | missense_variant | MODERATE | c.562G>A|p.Ala188Thr |
S299 |
| 23056 | BAA01g16670 | A01 | 8110815 | C | T | downstream_gene_variant | MODIFIER | c.*3156G>A| |
S250 |
| 23057 | BAA01g16660 | A01 | 8111086 | G | A | synonymous_variant | LOW | c.297C>T|p.Val99Val |
S94 |
| 23058 | BAA01g16660 | A01 | 8111105 | C | T | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S139 |
| 23059 | BAA01g16660 | A01 | 8113784 | C | T | upstream_gene_variant | MODIFIER | c.-2402G>A| |
S146 |
| 23060 | BAA01g16670 | A01 | 8114164 | C | T | missense_variant | MODERATE | c.1028G>A|p.Ser343Asn |
S88 |
| 23061 | BAA01g16670 | A01 | 8114173 | G | A | missense_variant | MODERATE | c.1019C>T|p.Ala340Val |
S56 |
| 23062 | BAA01g16670 | A01 | 8114497 | G | A | missense_variant | MODERATE | c.790C>T|p.Arg264Cys |
S263 |
| 23063 | BAA01g16670 | A01 | 8114653 | C | T | missense_variant | MODERATE | c.634G>A|p.Gly212Arg |
S19 |
| 23064 | BAA01g16670 | A01 | 8115123 | C | T | missense_variant | MODERATE | c.164G>A|p.Ser55Asn |
S192 |
| 23065 | BAA01g16670 | A01 | 8115183 | C | T | splice_region_variant&intron_variant | LOW | c.111-7G>A| |
S134 |
| 23066 | BAA01g16660 | A01 | 8115185 | G | A | upstream_gene_variant | MODIFIER | c.-3803C>T| |
S252 |
| 23067 | BAA01g16660 | A01 | 8115580 | G | A | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S163 |
| 23068 | BAA01g16660 | A01 | 8116187 | G | A | upstream_gene_variant | MODIFIER | c.-4805C>T| |
S178 |
| 23069 | BAA01g16670 | A01 | 8117349 | C | T | upstream_gene_variant | MODIFIER | c.-1828G>A| |
S100 |
| 23070 | BAA01g16680 | A01 | 8126856 | G | A | missense_variant | MODERATE | c.55G>A|p.Ala19Thr |
S195 |
| 23071 | BAA01g16680 | A01 | 8127408 | G | A | missense_variant | MODERATE | c.607G>A|p.Ala203Thr |
S263 |
| 23072 | BAA01g16680 | A01 | 8127676 | G | A | missense_variant | MODERATE | c.875G>A|p.Arg292Lys |
S37 |
| 23073 | BAA01g16680 | A01 | 8128140 | G | A | missense_variant | MODERATE | c.1252G>A|p.Asp418Asn |
S284 |
| 23074 | BAA01g16690 | A01 | 8129972 | C | T | upstream_gene_variant | MODIFIER | c.-1814C>T| |
S48 |
| 23075 | BAA01g16690 | A01 | 8130454 | C | T | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S62 |