| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31901 | BAA01g22060 | A01 | 11001065 | G | A | splice_donor_variant&intron_variant | HIGH | c.818+1G>A| |
S187 |
| 31902 | BAA01g22060 | A01 | 11001799 | C | T | synonymous_variant | LOW | c.1089C>T|p.Leu363Leu |
S167 |
| 31903 | BAA01g22050 | A01 | 11002352 | G | A | upstream_gene_variant | MODIFIER | c.-3341C>T| |
S299 |
| 31904 | BAA01g22060 | A01 | 11002923 | G | A | missense_variant | MODERATE | c.1645G>A|p.Asp549Asn |
S172 S217 |
| 31905 | BAA01g22060 | A01 | 11003417 | C | T | missense_variant | MODERATE | c.1963C>T|p.Arg655Trp |
S237 |
| 31906 | BAA01g22070 | A01 | 11005120 | C | T | missense_variant | MODERATE | c.2174G>A|p.Gly725Asp |
S43 |
| 31907 | BAA01g22070 | A01 | 11006042 | C | T | missense_variant | MODERATE | c.1318G>A|p.Val440Ile |
S148 S210 S30 S31 |
| 31908 | BAA01g22070 | A01 | 11006484 | C | T | synonymous_variant | LOW | c.876G>A|p.Val292Val |
S158 |
| 31909 | BAA01g22070 | A01 | 11007400 | C | T | upstream_gene_variant | MODIFIER | c.-41G>A| |
S139 |
| 31910 | BAA01g22080 | A01 | 11008183 | G | A | synonymous_variant | LOW | c.273C>T|p.Tyr91Tyr |
S131 |
| 31911 | BAA01g22070 | A01 | 11008496 | G | A | upstream_gene_variant | MODIFIER | c.-1137C>T| |
S72 S78 |
| 31912 | BAA01g22070 | A01 | 11009274 | C | T | upstream_gene_variant | MODIFIER | c.-1915G>A| |
S206 S26 |
| 31913 | BAA01g22090 | A01 | 11010358 | G | A | synonymous_variant | LOW | c.492C>T|p.Thr164Thr |
S298 |
| 31914 | BAA01g22090 | A01 | 11010457 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.394-1G>A| |
S205 |
| 31915 | BAA01g22090 | A01 | 11010593 | G | A | missense_variant | MODERATE | c.332C>T|p.Ala111Val |
S244 |
| 31916 | BAA01g22070 | A01 | 11010955 | G | A | upstream_gene_variant | MODIFIER | c.-3596C>T| |
S294 |
| 31917 | BAA01g22090 | A01 | 11011570 | C | T | missense_variant | MODERATE | c.14G>A|p.Gly5Glu |
S38 |
| 31918 | BAA01g22100 | A01 | 11013370 | C | T | missense_variant | MODERATE | c.850C>T|p.Pro284Ser |
S272 |
| 31919 | BAA01g22100 | A01 | 11013632 | G | A | splice_region_variant&intron_variant | LOW | c.1023+6G>A| |
S173 |
| 31920 | BAA01g22090 | A01 | 11013919 | G | A | upstream_gene_variant | MODIFIER | c.-2336C>T| |
S95 |
| 31921 | BAA01g22100 | A01 | 11014325 | C | T | synonymous_variant | LOW | c.1273C>T|p.Leu425Leu |
S206 S26 |
| 31922 | BAA01g22090 | A01 | 11015297 | G | A | upstream_gene_variant | MODIFIER | c.-3714C>T| |
S209 |
| 31923 | BAA01g22100 | A01 | 11017943 | C | T | downstream_gene_variant | MODIFIER | c.*2843C>T| |
S128 |
| 31924 | BAA01g22100 | A01 | 11018364 | G | A | downstream_gene_variant | MODIFIER | c.*3264G>A| |
S138 |
| 31925 | BAA01g22100 | A01 | 11018416 | C | T | downstream_gene_variant | MODIFIER | c.*3316C>T| |
S207 S260 |