| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 66951 | BAA01g35060-BAA01g35070 | A01 | 23457152 | C | A | intergenic_region | MODIFIER | n.23457152C>A| |
S249 |
| 66952 | BAA01g35060-BAA01g35070 | A01 | 23460874 | G | A | intergenic_region | MODIFIER | n.23460874G>A| |
S297 |
| 66953 | BAA01g35060-BAA01g35070 | A01 | 23480526 | C | T | intergenic_region | MODIFIER | n.23480526C>T| |
S233 |
| 66954 | BAA01g35060-BAA01g35070 | A01 | 23488484 | G | A | intergenic_region | MODIFIER | n.23488484G>A| |
S174 |
| 66955 | BAA01g35070 | A01 | 23488974 | C | T | downstream_gene_variant | MODIFIER | c.*4770G>A| |
S139 |
| 66956 | BAA01g35070 | A01 | 23489267 | C | T | downstream_gene_variant | MODIFIER | c.*4477G>A| |
S178 |
| 66957 | BAA01g35070 | A01 | 23491078 | G | A | downstream_gene_variant | MODIFIER | c.*2666C>T| |
S35 |
| 66958 | BAA01g35070 | A01 | 23492450 | C | T | downstream_gene_variant | MODIFIER | c.*1294G>A| |
S216 |
| 66959 | BAA01g35080 | A01 | 23505706 | G | A | downstream_gene_variant | MODIFIER | c.*1130C>T| |
S125 |
| 66960 | BAA01g35080 | A01 | 23509821 | C | T | intron_variant | MODIFIER | c.2437-792G>A| |
S272 |
| 66961 | BAA01g35090 | A01 | 23513761 | T | A | downstream_gene_variant | MODIFIER | c.*3236A>T| |
S243 |
| 66962 | BAA01g35080 | A01 | 23514193 | G | A | stop_gained | HIGH | c.973C>T|p.Gln325* |
S197 |
| 66963 | BAA01g35090 | A01 | 23514478 | C | T | downstream_gene_variant | MODIFIER | c.*2519G>A| |
S107 |
| 66964 | BAA01g35080 | A01 | 23516384 | C | T | upstream_gene_variant | MODIFIER | c.-1070G>A| |
S115 |
| 66965 | BAA01g35080 | A01 | 23516679 | C | T | upstream_gene_variant | MODIFIER | c.-1365G>A| |
S127 |
| 66966 | BAA01g35090 | A01 | 23517016 | G | A | missense_variant | MODERATE | c.1523C>T|p.Ser508Phe |
S296 |
| 66967 | BAA01g35090 | A01 | 23517377 | C | T | missense_variant | MODERATE | c.1162G>A|p.Glu388Lys |
S146 |
| 66968 | BAA01g35090 | A01 | 23518470 | G | A | missense_variant | MODERATE | c.142C>T|p.Leu48Phe |
S187 |
| 66969 | BAA01g35080 | A01 | 23519262 | G | A | upstream_gene_variant | MODIFIER | c.-3948C>T| |
S207 |
| 66970 | BAA01g35080 | A01 | 23519353 | C | T | upstream_gene_variant | MODIFIER | c.-4039G>A| |
S18 |
| 66971 | BAA01g35080 | A01 | 23519367 | C | T | upstream_gene_variant | MODIFIER | c.-4053G>A| |
S185 |
| 66972 | BAA01g35080 | A01 | 23519485 | G | A | upstream_gene_variant | MODIFIER | c.-4171C>T| |
S262 |
| 66973 | BAA01g35090 | A01 | 23521099 | C | T | upstream_gene_variant | MODIFIER | c.-2488G>A| |
S20 |
| 66974 | BAA01g35090 | A01 | 23523530 | G | A | upstream_gene_variant | MODIFIER | c.-4919C>T| |
S176 |
| 66975 | BAA01g35100 | A01 | 23524663 | A | G | upstream_gene_variant | MODIFIER | c.-93A>G| |
S269 |