| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 30951 | BAA01g21560 | A01 | 10701932 | G | A | upstream_gene_variant | MODIFIER | c.-4058G>A| |
S199 |
| 30952 | BAA01g21560 | A01 | 10702207 | C | T | upstream_gene_variant | MODIFIER | c.-3783C>T| |
S16 |
| 30953 | BAA01g21560 | A01 | 10702865 | G | A | upstream_gene_variant | MODIFIER | c.-3125G>A| |
S75 S81 |
| 30954 | BAA01g21560 | A01 | 10702912 | C | T | upstream_gene_variant | MODIFIER | c.-3078C>T| |
S256 |
| 30955 | BAA01g21560 | A01 | 10703009 | G | A | upstream_gene_variant | MODIFIER | c.-2981G>A| |
S34 |
| 30956 | BAA01g21560 | A01 | 10703893 | C | T | upstream_gene_variant | MODIFIER | c.-2097C>T| |
S305 |
| 30957 | BAA01g21560 | A01 | 10704082 | C | T | upstream_gene_variant | MODIFIER | c.-1908C>T| |
S53 |
| 30958 | BAA01g21560 | A01 | 10704109 | G | A | upstream_gene_variant | MODIFIER | c.-1881G>A| |
S109 |
| 30959 | BAA01g21560 | A01 | 10704804 | C | T | upstream_gene_variant | MODIFIER | c.-1186C>T| |
S166 |
| 30960 | BAA01g21560 | A01 | 10705487 | C | T | upstream_gene_variant | MODIFIER | c.-503C>T| |
S100 |
| 30961 | BAA01g21560 | A01 | 10705503 | C | T | upstream_gene_variant | MODIFIER | c.-487C>T| |
S150 |
| 30962 | BAA01g21560 | A01 | 10705721 | G | A | upstream_gene_variant | MODIFIER | c.-269G>A| |
S275 |
| 30963 | BAA01g21560 | A01 | 10707016 | C | T | downstream_gene_variant | MODIFIER | c.*694C>T| |
S286 |
| 30964 | BAA01g21560 | A01 | 10707306 | C | T | downstream_gene_variant | MODIFIER | c.*984C>T| |
S111 |
| 30965 | BAA01g21570 | A01 | 10707672 | C | T | missense_variant | MODERATE | c.1060G>A|p.Glu354Lys |
S247 |
| 30966 | BAA01g21570 | A01 | 10709088 | G | A | synonymous_variant | LOW | c.204C>T|p.Leu68Leu |
S288 |
| 30967 | BAA01g21570 | A01 | 10709132 | C | T | missense_variant | MODERATE | c.160G>A|p.Ala54Thr |
S139 |
| 30968 | BAA01g21580 | A01 | 10709318 | C | T | upstream_gene_variant | MODIFIER | c.-3687C>T| |
S117 |
| 30969 | BAA01g21580 | A01 | 10709433 | G | A | upstream_gene_variant | MODIFIER | c.-3572G>A| |
S257 |
| 30970 | BAA01g21570 | A01 | 10709684 | G | A | splice_region_variant&intron_variant | LOW | c.156+6C>T| |
S163 |
| 30971 | BAA01g21570 | A01 | 10709794 | G | A | missense_variant | MODERATE | c.52C>T|p.Arg18Cys |
S281 |
| 30972 | BAA01g21570 | A01 | 10709836 | C | T | missense_variant | MODERATE | c.10G>A|p.Gly4Ser |
S18 |
| 30973 | BAA01g21570 | A01 | 10710109 | G | A | upstream_gene_variant | MODIFIER | c.-264C>T| |
S197 |
| 30974 | BAA01g21570 | A01 | 10710862 | C | T | upstream_gene_variant | MODIFIER | c.-1017G>A| |
S135 |
| 30975 | BAA01g21570 | A01 | 10711574 | G | A | upstream_gene_variant | MODIFIER | c.-1729C>T| |
S33 |