| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 25101 | BAA01g18030 | A01 | 8828448 | G | A | missense_variant | MODERATE | c.1736G>A|p.Arg579Lys |
S234 |
| 25102 | BAA01g18020 | A01 | 8828635 | C | T | downstream_gene_variant | MODIFIER | c.*4463C>T| |
S18 |
| 25103 | BAA01g18030 | A01 | 8829247 | C | T | downstream_gene_variant | MODIFIER | c.*717C>T| |
S198 |
| 25104 | BAA01g18040 | A01 | 8830989 | G | A | upstream_gene_variant | MODIFIER | c.-595C>T| |
S45 |
| 25105 | BAA01g18050 | A01 | 8831611 | C | T | synonymous_variant | LOW | c.396G>A|p.Thr132Thr |
S100 |
| 25106 | BAA01g18050 | A01 | 8831612 | G | A | missense_variant | MODERATE | c.395C>T|p.Thr132Met |
S246 |
| 25107 | BAA01g18050 | A01 | 8831942 | G | A | missense_variant | MODERATE | c.65C>T|p.Thr22Ile |
S246 |
| 25108 | BAA01g18040 | A01 | 8832042 | G | A | upstream_gene_variant | MODIFIER | c.-1648C>T| |
S15 S3 |
| 25109 | BAA01g18040 | A01 | 8833397 | C | T | upstream_gene_variant | MODIFIER | c.-3003G>A| |
S255 |
| 25110 | BAA01g18040 | A01 | 8833673 | C | T | upstream_gene_variant | MODIFIER | c.-3279G>A| |
S233 |
| 25111 | BAA01g18040 | A01 | 8833914 | C | T | upstream_gene_variant | MODIFIER | c.-3520G>A| |
S35 |
| 25112 | BAA01g18040 | A01 | 8834439 | G | A | upstream_gene_variant | MODIFIER | c.-4045C>T| |
S37 |
| 25113 | BAA01g18040 | A01 | 8835128 | C | T | upstream_gene_variant | MODIFIER | c.-4734G>A| |
S166 |
| 25114 | BAA01g18050 | A01 | 8836651 | C | T | upstream_gene_variant | MODIFIER | c.-4645G>A| |
S242 |
| 25115 | BAA01g18060 | A01 | 8837398 | T | A | downstream_gene_variant | MODIFIER | c.*1548A>T| |
S241 |
| 25116 | BAA01g18060 | A01 | 8840097 | T | C | missense_variant | MODERATE | c.1118A>G|p.Glu373Gly |
S255 |
| 25117 | BAA01g18060 | A01 | 8840118 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1098-1G>A| |
S247 |
| 25118 | BAA01g18060 | A01 | 8840237 | C | T | missense_variant | MODERATE | c.1064G>A|p.Arg355Lys |
S167 |
| 25119 | BAA01g18060 | A01 | 8840920 | G | A | intron_variant | MODIFIER | c.688-151C>T| |
S172 S217 |
| 25120 | BAA01g18060 | A01 | 8842003 | C | T | missense_variant | MODERATE | c.589G>A|p.Gly197Arg |
S182 |
| 25121 | BAA01g18060 | A01 | 8842349 | G | A | splice_region_variant&intron_variant | LOW | c.450+3C>T| |
S45 |
| 25122 | BAA01g18060 | A01 | 8842856 | G | A | intron_variant | MODIFIER | c.175-15C>T| |
S156 |
| 25123 | BAA01g18060 | A01 | 8842942 | G | A | intron_variant | MODIFIER | c.175-101C>T| |
S246 |
| 25124 | BAA01g18060 | A01 | 8843846 | G | A | upstream_gene_variant | MODIFIER | c.-616C>T| |
S209 |
| 25125 | BAA01g18060 | A01 | 8845073 | C | T | upstream_gene_variant | MODIFIER | c.-1843G>A| |
S223 |