| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 24151 | BAA01g17500 | A01 | 8518178 | T | A | downstream_gene_variant | MODIFIER | c.*3088T>A| |
S120 |
| 24152 | BAA01g17530 | A01 | 8519741 | C | T | upstream_gene_variant | MODIFIER | c.-3694C>T| |
S79 S84 |
| 24153 | BAA01g17530 | A01 | 8520512 | G | A | upstream_gene_variant | MODIFIER | c.-2923G>A| |
S301 S304 |
| 24154 | BAA01g17530 | A01 | 8521021 | G | A | upstream_gene_variant | MODIFIER | c.-2414G>A| |
S159 S243 |
| 24155 | BAA01g17530 | A01 | 8521320 | C | T | upstream_gene_variant | MODIFIER | c.-2115C>T| |
S35 |
| 24156 | BAA01g17530 | A01 | 8521852 | G | A | upstream_gene_variant | MODIFIER | c.-1583G>A| |
S173 |
| 24157 | BAA01g17530 | A01 | 8522137 | C | T | upstream_gene_variant | MODIFIER | c.-1298C>T| |
S2 |
| 24158 | BAA01g17520 | A01 | 8522341 | C | T | synonymous_variant | LOW | c.162G>A|p.Glu54Glu |
S148 S30 S31 |
| 24159 | BAA01g17520 | A01 | 8523191 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S288 |
| 24160 | BAA01g17520 | A01 | 8523933 | G | A | upstream_gene_variant | MODIFIER | c.-1431C>T| |
S257 |
| 24161 | BAA01g17520 | A01 | 8526524 | C | T | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S113 |
| 24162 | BAA01g17520 | A01 | 8527201 | C | T | upstream_gene_variant | MODIFIER | c.-4699G>A| |
S19 |
| 24163 | BAA01g17530 | A01 | 8527572 | C | T | downstream_gene_variant | MODIFIER | c.*2299C>T| |
S18 |
| 24164 | BAA01g17530 | A01 | 8527576 | C | T | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S267 |
| 24165 | BAA01g17540 | A01 | 8527606 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.373-1G>A| |
S197 |
| 24166 | BAA01g17540 | A01 | 8527635 | G | A | missense_variant | MODERATE | c.401G>A|p.Gly134Glu |
S58 |
| 24167 | BAA01g17540 | A01 | 8527673 | C | T | missense_variant | MODERATE | c.439C>T|p.Leu147Phe |
S125 |
| 24168 | BAA01g17540 | A01 | 8527901 | C | A | synonymous_variant | LOW | c.540C>A|p.Leu180Leu |
S265 |
| 24169 | BAA01g17540 | A01 | 8528529 | G | A | missense_variant | MODERATE | c.928G>A|p.Asp310Asn |
S263 |
| 24170 | BAA01g17540 | A01 | 8528658 | T | G | missense_variant | MODERATE | c.1057T>G|p.Phe353Val |
S155 S163 S170 S231 S241 S283 S3 S62 S76 |
| 24171 | BAA01g17540 | A01 | 8528659 | T | G | missense_variant | MODERATE | c.1058T>G|p.Phe353Cys |
S155 S163 S170 S231 S241 S283 S3 S62 S76 |
| 24172 | BAA01g17540 | A01 | 8528706 | G | A | missense_variant | MODERATE | c.1105G>A|p.Glu369Lys |
S280 |
| 24173 | BAA01g17540 | A01 | 8529065 | G | A | synonymous_variant | LOW | c.1464G>A|p.Gln488Gln |
S172 S217 |
| 24174 | BAA01g17540 | A01 | 8529146 | C | T | synonymous_variant | LOW | c.1545C>T|p.Thr515Thr |
S198 |
| 24175 | BAA01g17540 | A01 | 8529170 | C | T | synonymous_variant | LOW | c.1569C>T|p.Phe523Phe |
S267 |